Hit 1

Reference List

FAIDE(1); FLST(13); XREF(3); INP(6); CDER(2); MP(9); CRYPH(2); NMR(1); IR(1); UV(2); MS(1); POT(1); FINFO(2); RX(4); CNR(20)

Substance (1 of 1)
Beilstein Registry Number90739
Beilstein Preferred RN94-62-2
CAS Registry Number94-62-2; 495-91-0; 7780-20-3; 30511-76-3; 30511-77-4
Chemical Name1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine; 1-Piperinoyl-piperidin; piperine
Autoname5-benzo[1,3]dioxol-5-yl-1-piperidin-1-yl-penta-2,4-dien-1-one
Molecular FormulaC17H19NO3
Molecular Weight285.34
Lawson Number24081; 22876
Compound Typeheterocyclic
Constitution ID38159
Tautomer ID14686
Beilstein Reference5-20-03-00469; 6-20
Entry Date1988/06/27
Update Date1994/01/18

Reference (1 of 20)
Citation Number119906
Document TypeJournal
AuthorsStoklosa,K.
CODENBSCFAS
Journal TitleBull.Soc.Chim.Fr.
Language CodeFR
Publication Year1969
Page3802-3806

Reference (2 of 20)
Citation Number2605306
Document TypeJournal
AuthorsLloyd et al.
CODENJACSAT
Journal TitleJ.Amer.Chem.Soc.
(Series) Volume82
Publication Year1960
Page3791

Reference (3 of 20)
Citation Number2835455
Document TypeJournal
AuthorsGupta et al.
CODENPYTCAS
Journal TitlePhytochemistry
(Series) Volume11
Publication Year1972
Page2646

Reference (4 of 20)
Citation Number3133321
Document TypeJournal
AuthorsDutta et al.
CODENIJSBDB
Journal TitleIndian J.Chem.Sect.B
(Series) Volume15
Publication Year1977
Page583

Reference (5 of 20)
Citation Number3133481
Document TypeJournal
AuthorsLurik et al.
CODENJGCHA4; ZOKHA4
Journal TitleJ.Gen.Chem.USSR (Engl.Transl.); Zh.Obshch.Khim.
(Series) Volume45; 45
Publication Year1975; 1975
Page2246; 2287

Reference (6 of 20)
Citation Number3141536
Document TypeJournal
AuthorsMazeau; Zarzycki
CODENCHDCAQ
Journal TitleC.R.Hebd.Seances Acad.Sci.Ser.C
(Series) Volume281
Publication Year1975
Page583,584

Reference (7 of 20)
Citation Number3141959
Document TypeJournal
AuthorsLoder et al.
CODENAJCHAS
Journal TitleAust.J.Chem.
(Series) Volume22
Publication Year1969
Page1531,1538

Reference (8 of 20)
Citation Number3142215
Document TypeJournal
AuthorsBanerji; Dhara
CODENPYTCAS
Journal TitlePhytochemistry
(Series) Volume13
Publication Year1974
Page2327

Reference (9 of 20)
Citation Number3142495
Document TypeJournal
AuthorsVashkov et al.
CODENRZKHAR
Journal TitleRef.Zh.Khim.
Journal/Review Without CODENChem.Abstr.
(Series) Volume17; 81
Number13234b
Publication Year1973; 1974
Page508

Reference (10 of 20)
Citation Number3214879
Document TypeJournal
AuthorsFeugeas
CODENBSCFAS
Journal TitleBull.Soc.Chim.Fr.
Publication Year1964
Page1892

Reference (11 of 20)
Citation Number3220501
Document TypeJournal
AuthorsNormant; Feugeas
CODENCOREAF
Journal TitleC.R.Hebd.Seances Acad.Sci.
(Series) Volume258
Publication Year1964
Page2846

Reference (12 of 20)
Citation Number3228104
Document TypeJournal
AuthorsGraham
CODENJPMSAE
Journal TitleJ.Pharm.Sci.
(Series) Volume54
Publication Year1965
Page319

Reference (13 of 20)
Citation Number3239881
Document TypeJournal
AuthorsMishra; Tewari
CODENJPMSAE
Journal TitleJ.Pharm.Sci.
(Series) Volume53
Publication Year1964
Page1423

Reference (14 of 20)
Citation Number3281384
Document TypeJournal
AuthorsTraxler
CODENJAFCAU
Journal TitleJ.Agric.Food Chem.
(Series) Volume19
Publication Year1971
Page1135,1137

Reference (15 of 20)
Citation Number3341233
Document TypeJournal
AuthorsSingh et al.
CODENJICSAH
Journal TitleJ.Indian Chem.Soc.
(Series) Volume53
Publication Year1976
Page1162

Reference (16 of 20)
Citation Number3633748
Document TypeJournal
AuthorsBohnsack
CODENRSARAQ
Journal TitleRiechst.Aromen
(Series) Volume15
Publication Year1965
Page77

Reference (17 of 20)
Citation Number3678903
Document TypeJournal
AuthorsBordner; Mullins
CODENCSCMCS
Journal TitleCryst.Struct.Commun.
(Series) Volume3
Publication Year1974
Page693

Reference (18 of 20)
Citation Number4815504
Document TypeJournal
AuthorsKulka
CODENJAFCAU
Journal TitleJ.Agric.Food Chem.
(Series) Volume15
Publication Year1967
Page48,51

Reference (19 of 20)
Citation Number5546680
Document TypeJournal
AuthorsMandai, Tadakatsu; Moriyama, Tadashi; Tsujimoto, Koichiro; Kawada, Mikio; Otera, Junzo
CODENTELEAY
Journal TitleTetrahedron Lett.
Language CodeEN
(Series) Volume27
Number5
Publication Year1986
Page603-606

Reference (20 of 20)
Citation Number5686470
Document TypeJournal
AuthorsHoelzel, Claus; Spiteller, Gerhard
CODENLACHDL
Journal TitleLiebigs Ann.Chem.
Language CodeGE
Number7
Publication Year1984
Page1319-1331

Reaction (1 of 4)
Reaction ID2627935
Reactant BRN4613019
Reactantacetic acid 1-(benzenesulfonyl-benzo[1,3]dioxol-5-yl-methyl)-4-oxo-4-piperidin-1-yl-butyl ester
Product BRN90739; 90741
Product1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine; 1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Reagentt-BuOK
Solvent2-methyl-propan-2-ol
Time12 hour(s)
Other ConditionsAmbient temperature
CommentYield given. Yields of byproduct given
Citation Pointer5546680; Journal; Mandai, Tadakatsu; Moriyama, Tadashi; Tsujimoto, Koichiro; Kawada, Mikio; Otera, Junzo; TELEAY; Tetrahedron Lett.; EN; 27; 5; 1986; 603-606;

Reaction (2 of 4)
Reaction ID3863768
Reactant BRN90739
Reactant1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine
Product BRN5564597
Product5-(3,4-Dihydroxyphenyl)-2,4-pentadiensaeure-piperidid
No. of Reaction Details1
Reaction ClassificationPreparation
Yield86 percent (BRN=5564597)
Reagent0.5 M BBr3, 0.5 M sodium acetate buffer (pH=5)
SolventCH2Cl2
Time72 hour(s)
Other ConditionsAmbient temperature
Citation Pointer5686470; Journal; Hoelzel, Claus; Spiteller, Gerhard; LACHDL; Liebigs Ann.Chem.; GE; 7; 1984; 1319-1331;

Reaction (3 of 4)
Reaction ID5392514
Reactant BRN90739
Reactant1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine
No. of Reaction Details2
Reaction ClassificationChemical behaviour (half reaction)
Subject StudiedKinetics
Citation Pointer119906; Journal; Stoklosa,K.; BSCFAS; Bull.Soc.Chim.Fr.; FR; 1969; 3802-3806;

Reaction (4 of 4)
Reaction ID5714783
Product BRN90739
Product1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation (half reaction)
Citation Pointer3220501; Journal; Normant; Feugeas; COREAF; C.R.Hebd.Seances Acad.Sci.; 258; 1964; 2846;3214879; Journal; Feugeas; BSCFAS; Bull.Soc.Chim.Fr.; 1964; 1892;

Isolation from Natural Product (1 of 6)
Isolation from Natural Productaus Piper nigrum L.
Citation Pointer3281384; Journal; Traxler; JAFCAU; J.Agric.Food Chem.; 19; 1971; 1135,1137;

Isolation from Natural Product (2 of 6)
Isolation from Natural Productaus Pfeffer
Citation Pointer3633748; Journal; Bohnsack; RSARAQ; Riechst.Aromen; 15; 1965; 77;

Isolation from Natural Product (3 of 6)
Isolation from Natural Productaus Stengel von Piper nigrum Linn.
Citation Pointer3341233; Journal; Singh et al.; JICSAH; J.Indian Chem.Soc.; 53; 1976; 1162;

Isolation from Natural Product (4 of 6)
Isolation from Natural Productaus Piper chaba
Citation Pointer3239881; Journal; Mishra; Tewari; JPMSAE; J.Pharm.Sci.; 53; 1964; 1423;

Isolation from Natural Product (5 of 6)
Isolation from Natural Productaus Piper longum Linn.
Citation Pointer3133321; Journal; Dutta et al.; IJSBDB; Indian J.Chem.Sect.B; 15; 1977; 583;

Isolation from Natural Product (6 of 6)
Isolation from Natural Productaus Piper nepalense
Citation Pointer2835455; Journal; Gupta et al.; PYTCAS; Phytochemistry; 11; 1972; 2646;

Derivative (1 of 2)
CommentHydrobromid: C17H19NO3*HBr: aus Piperin in Bzl., ges. benzol. HBr-Lsg.; F: 170grad
Citation Pointer3220501; Journal; Normant; Feugeas; COREAF; C.R.Hebd.Seances Acad.Sci.; 258; 1964; 2846;

Derivative (2 of 2)
CommentHydrobromid: F: 170grad (aus Bzl.; Kofler-App:)
Citation Pointer3214879; Journal; Feugeas; BSCFAS; Bull.Soc.Chim.Fr.; 1964; 1892;

Crossfile Reference (1 of 3)
NamePiperine; for synthesis
Crossfile SourceE.Merck, Darmstadt
External Access ID821036

Crossfile Reference (2 of 3)
NamePIPERINE, 97 PERCENT
Crossfile SourceAldrich
External Access IDP49007

Crossfile Reference (3 of 3)
Namepiperine
Crossfile SourceEINECS
External Access ID202-348-0

Melting Point (1 of 9)
Melting Point129.2 - 130.5
Citation Pointer3281384; Journal; Traxler; JAFCAU; J.Agric.Food Chem.; 19; 1971; 1135,1137;

Melting Point (2 of 9)
Melting Point129
Solventdiethyl ether
Citation Pointer3220501; Journal; Normant; Feugeas; COREAF; C.R.Hebd.Seances Acad.Sci.; 258; 1964; 2846;3214879; Journal; Feugeas; BSCFAS; Bull.Soc.Chim.Fr.; 1964; 1892;

Melting Point (3 of 9)
Melting Point128
Citation Pointer119906; Journal; Stoklosa,K.; BSCFAS; Bull.Soc.Chim.Fr.; FR; 1969; 3802-3806;

Melting Point (4 of 9)
Melting Point128 - 129.5
Citation Pointer3142495; Journal; Vashkov et al.; RZKHAR; Ref.Zh.Khim.; 17; 1973; 508; Chem.Abstr.; 81; 13234b; 1974;3633748; Journal; Bohnsack; RSARAQ; Riechst.Aromen; 15; 1965; 77;

Melting Point (5 of 9)
Melting Point129 - 130
Citation Pointer2835455; Journal; Gupta et al.; PYTCAS; Phytochemistry; 11; 1972; 2646;

Melting Point (6 of 9)
Melting Point128 - 129
Citation Pointer4815504; Journal; Kulka; JAFCAU; J.Agric.Food Chem.; 15; 1967; 48,51;

Melting Point (7 of 9)
Melting Point127 - 129
Citation Pointer3142215; Journal; Banerji; Dhara; PYTCAS; Phytochemistry; 13; 1974; 2327;

Melting Point (8 of 9)
Melting Point128 - 129
Citation Pointer3133481; Journal; Lurik et al.; JGCHA4; J.Gen.Chem.USSR (Engl.Transl.); 45; 1975; 2246; ZOKHA4; Zh.Obshch.Khim.; 45; 1975; 2287;

Melting Point (9 of 9)
Melting Point120 - 129
Citation Pointer3341233; Journal; Singh et al.; JICSAH; J.Indian Chem.Soc.; 53; 1976; 1162;

Crystal Phase (1 of 2)
DescriptionCrystal habit
Citation Pointer3678903; Journal; Bordner; Mullins; CSCMCS; Cryst.Struct.Commun.; 3; 1974; 693;

Crystal Phase (2 of 2)
DescriptionCrystal growth
Citation Pointer3141536; Journal; Mazeau; Zarzycki; CHDCAQ; C.R.Hebd.Seances Acad.Sci.Ser.C; 281; 1975; 583,584;

Nuclear Magnetic Resonance (1 of 1)
DescriptionNMR
Citation Pointer3133481; Journal; Lurik et al.; JGCHA4; J.Gen.Chem.USSR (Engl.Transl.); 45; 1975; 2246; ZOKHA4; Zh.Obshch.Khim.; 45; 1975; 2287;

Infrared Spectra (1 of 1)
DescriptionIR
Citation Pointer3133481; Journal; Lurik et al.; JGCHA4; J.Gen.Chem.USSR (Engl.Transl.); 45; 1975; 2246; ZOKHA4; Zh.Obshch.Khim.; 45; 1975; 2287;3142215; Journal; Banerji; Dhara; PYTCAS; Phytochemistry; 13; 1974; 2327;3220501; Journal; Normant; Feugeas; COREAF; C.R.Hebd.Seances Acad.Sci.; 258; 1964; 2846;

Ultraviolet Spectra (1 of 2)
DescriptionAbsorption maxima
Citation Pointer3220501; Journal; Normant; Feugeas; COREAF; C.R.Hebd.Seances Acad.Sci.; 258; 1964; 2846;

Ultraviolet Spectra (2 of 2)
DescriptionUV/VIS
Citation Pointer3133481; Journal; Lurik et al.; JGCHA4; J.Gen.Chem.USSR (Engl.Transl.); 45; 1975; 2246; ZOKHA4; Zh.Obshch.Khim.; 45; 1975; 2287;3281384; Journal; Traxler; JAFCAU; J.Agric.Food Chem.; 19; 1971; 1135,1137;

Mass Spectrum (1 of 1)
Citation Pointer3142215; Journal; Banerji; Dhara; PYTCAS; Phytochemistry; 13; 1974; 2327;

Electrochemical Characteristics (1 of 1)
Descriptionpolarographic half-wave potential
Citation Pointer3133481; Journal; Lurik et al.; JGCHA4; J.Gen.Chem.USSR (Engl.Transl.); 45; 1975; 2246; ZOKHA4; Zh.Obshch.Khim.; 45; 1975; 2287;

Further Information (1 of 2)
Citation Pointer3141959; Journal; Loder et al.; AJCHAS; Aust.J.Chem.; 22; 1969; 1531,1538;3228104; Journal; Graham; JPMSAE; J.Pharm.Sci.; 54; 1965; 319;

Further Information (2 of 2)
Citation Pointer2605306; Journal; Lloyd et al.; JACSAT; J.Amer.Chem.Soc.; 82; 1960; 3791;

Hit 2

Reference List

FAIDE(1); FLST(23); XREF(4); RSTR(1); INP(30); CDER(1); CPD(2); MP(19); CRYPH(8); SP(1); DEN(4); DV(1); RI(1); NMR(15); IR(12); UV(10); MS(5); ELE(1); DE(3); POT(1); SLB(8); BSPM(1); PHARM(60); RX(31); CNR(126)

Substance (1 of 1)
Beilstein Registry Number90741
Beilstein Preferred RN94-62-2
CAS Registry Number94-62-2; 495-91-0; 7780-20-3; 30511-76-3; 30511-77-4
Chemical Name1-trans,trans-piperinoyl-piperidine; piperine; (E,E)-1-[5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-piperidine
Autoname5-benzo[1,3]dioxol-5-yl-1-piperidin-1-yl-penta-2,4-dien-1-one
Molecular FormulaC17H19NO3
Molecular Weight285.34
Lawson Number24081; 22876
Structure KeywordStereo compound
Compound Typeheterocyclic
Constitution ID38159
Tautomer ID18563
Beilstein Reference0-20-00-00079; 1-20-00-00023; 2-20-00-00053; 4-20-00-01341; 5-20-03-00469; 6-20
Entry Date1988/06/27
Update Date2002/04/29

Reference (1 of 126)
Citation Number156361
Document TypeJournal
AuthorsOkogun,J.I.; Ekong,D.E.U.
CODENJCPRB4
Journal TitleJ.Chem.Soc.Perkin Trans.1
Language CodeEN
Publication Year1974
Page2195-2198

Reference (2 of 126)
Citation Number502948
Document TypeJournal
AuthorsPeinemann
CODENARPMAS
Journal TitleArch.Pharm.(Weinheim Ger.)
(Series) Volume234
Publication Year1896
Page258

Reference (3 of 126)
Citation Number503101
Document TypeJournal
AuthorsFittig; Mielck
CODENJLACBF; JLACBF
Journal TitleJustus Liebigs Ann. Chem.; Justus Liebigs Ann. Chem.
(Series) Volume152; 172
Publication Year1869; 1874
Page52, 54; 140, 152

Reference (4 of 126)
Citation Number505033
Document TypeJournal
AuthorsBorsche
CODENCHBEAM
Journal TitleChem.Ber.
(Series) Volume44
Publication Year1911
Page2945

Reference (5 of 126)
Citation Number505376
Document TypeJournal
AuthorsDehn
CODENJACSAT
Journal TitleJ.Amer.Chem.Soc.
(Series) Volume39
Publication Year1917
Page1400

Reference (6 of 126)
Citation Number505581
Document TypeJournal
AuthorsDobbie; Fox
CODENJCSOA9
Journal TitleJ.Chem.Soc.
(Series) Volume103
Publication Year1913
Page1194

Reference (7 of 126)
Citation Number507531
Document TypeJournal
AuthorsLohaus
CODENJPCEAO
Journal TitleJ.Prakt.Chem.
(Series) Volume<2> 119
Publication Year1928
Page258

Reference (8 of 126)
Citation Number511899
Document TypeJournal
AuthorsBriggs et al.
CODENANCHAM
Journal TitleAnal.Chem.
(Series) Volume29
Publication Year1957
Page904, 905

Reference (9 of 126)
Citation Number520054
Document TypeJournal
AuthorsLohaus; Gall
CODENJLACBF
Journal TitleJustus Liebigs Ann. Chem.
(Series) Volume517
Publication Year1935
Page278, 284

Reference (10 of 126)
Citation Number529237
Document TypeJournal
AuthorsSpring; Stark
CODENJCSOA9
Journal TitleJ.Chem.Soc.
Publication Year1950
Page1177, 1178

Reference (11 of 126)
Citation Number536898
Document TypeJournal
AuthorsKopzik et al.
CODENVMUNAE
Journal TitleVestn.Mosk.Univ.
Journal/Review Without CODENChem.Abstr.
(Series) Volume13
Number6
Publication Year1958; 1959
Page91, 94; 15673

Reference (12 of 126)
Citation Number559145
Document TypeJournal
AuthorsWester
CODENCHZEA6
Journal TitleChem.Zentralbl.
Language CodeGE
(Series) Volume86
NumberI
Publication Year1915
Page248

Reference (13 of 126)
Citation Number562634
Document TypeJournal
AuthorsPucher; Dehn
CODENJACSAT
Journal TitleJ.Amer.Chem.Soc.
(Series) Volume43
Publication Year1921
Page1755

Reference (14 of 126)
Citation Number621663
Document TypeJournal
AuthorsSkita; Franck
CODENCHBEAM
Journal TitleChem.Ber.
(Series) Volume44
Publication Year1911
Page2866

Reference (15 of 126)
Citation Number625129
Document TypeJournal
AuthorsArnall
CODENJCSOA9
Journal TitleJ.Chem.Soc.
(Series) Volume117
Publication Year1920
Page837

Reference (16 of 126)
Citation Number625734
Document TypeJournal
Authorsv. Weisse; Meyer-Levy
CODENJCPBAN; CHZEA6
Journal TitleJ.Chim.Phys.Phys.Chim.Biol.; Chem.Zentralbl.
Language CodeGE
(Series) Volume14; 87
NumberII
Publication Year1916; 1916
Page276; 1030

Reference (17 of 126)
Citation Number625737
Document TypeJournal
AuthorsZeehuisen
CODENAEPPAE; CHZEA6
Journal TitleNaunyn-Schmiedeberg's Arch.Exp.Pathol.Pharmakol.; Chem.Zentralbl.
Language CodeGE
(Series) Volume86; 91
NumberIII
Publication Year1920; 1920
Page366; 668

Reference (18 of 126)
Citation Number636409
Document TypeJournal
AuthorsJanot; Chaigneau
CODENCOREAF
Journal TitleC.R.Hebd.Seances Acad.Sci.
(Series) Volume225
Publication Year1947
Page1371

Reference (19 of 126)
Citation Number642911
Document TypeJournal
AuthorsPleat et al.
CODENJPHAA3
Journal TitleJ.Am.Pharm.Assoc.
(Series) Volume40
Publication Year1951
Page107, 108

Reference (20 of 126)
Citation Number740972
Document TypeJournal
AuthorsKolthoff
CODENBIZEA2; PHJOAV; CHZEA6
Journal TitleBiochem.Z.; Pharm.J.; Chem.Zentralbl.
Language CodeGE
(Series) Volume162; 118; 98
NumberI
Publication Year1925; 1927
Page340; 126; 2116

Reference (21 of 126)
Citation Number745868
Document TypeJournal
AuthorsPaterno
CODENGCITA9
Journal TitleGazz.Chim.Ital.
(Series) Volume44 II
Publication Year1914
Page104, 106

Reference (22 of 126)
Citation Number784769
Document TypePatent
Patent AuthorLever Brothers Co.
Patent NumberUS 2085064
Patent Year1935

Reference (23 of 126)
Citation Number960841
Document TypeJournal
Authorsv. Babo; Keller
CODENJPCEAO; JCVWAE
Journal TitleJ.Prakt.Chem.; Jahresber.Fortschr.Chem.Verw.Theile Anderer Wiss.
(Series) Volume<1> 72
Publication Year1857; 1857
Page55; 413

Reference (24 of 126)
Citation Number960844
Document TypeJournal
AuthorsRuegheimer
CODENCHBEAM
Journal TitleChem.Ber.
(Series) Volume15
Publication Year1882
Page1391

Reference (25 of 126)
Citation Number960845
Document TypeJournal
AuthorsPeckolt
Journal/Review Without CODENApoth. Ztg.
(Series) Volume10
Page471

Reference (26 of 126)
Citation Number960846
Document TypeJournal
AuthorsHerlant
CODENPHJOAV
Journal TitlePharm.J.
(Series) Volume<3> 25
Page643

Reference (27 of 126)
Citation Number960847
Document TypeJournal
AuthorsStenhouse
CODENPHJOAV; JLACBF
Journal TitlePharm.J.; Justus Liebigs Ann. Chem.
(Series) Volume<1> 14; 95
Publication Year1855
Page363; 106

Reference (28 of 126)
Citation Number960848
Document TypeJournal
AuthorsWangerin
Journal/Review Without CODENPharm. Ztg.
(Series) Volume48
Page454

Reference (29 of 126)
Citation Number960849
Document TypeJournal
AuthorsBauer; Hilger
CODENCHZEA6
Journal TitleChem.Zentralbl.
Language CodeGE
(Series) Volume67
NumberI
Publication Year1896
Page1214

Reference (30 of 126)
Citation Number960850
Document TypeJournal
AuthorsVarrentrapp; Will
CODENJLACBF
Journal TitleJustus Liebigs Ann. Chem.
(Series) Volume39
Publication Year1841
Page283

Reference (31 of 126)
Citation Number960851
Document TypeJournal
AuthorsRegnault
CODENANCPAC
Journal TitleAnn.Chim.(Paris)
(Series) Volume<2> 68
Publication Year1838
Page158

Reference (32 of 126)
Citation Number960852
Document TypeJournal
AuthorsLiebig
CODENJLACBF
Journal TitleJustus Liebigs Ann. Chem.
(Series) Volume6
Publication Year1833
Page36

Reference (33 of 126)
Citation Number960853
Document TypeJournal
AuthorsPelletier
CODENANCPAC; JLACBF
Journal TitleAnn.Chim.(Paris); Justus Liebigs Ann. Chem.
(Series) Volume<2> 51; 6
Publication Year1832; 1833
Page199; 33

Reference (34 of 126)
Citation Number960854
Document TypeJournal
AuthorsPelletier
CODENANCPAC
Journal TitleAnn.Chim.(Paris)
Journal/Review Without CODENSchw.
(Series) Volume<2> 16; 32
Publication Year1821
Page344; 436

Reference (35 of 126)
Citation Number960855
Document TypeJournal
AuthorsOerstedt
Journal/Review Without CODENSchweiggers Journ. f. Chemie u. Physik
(Series) Volume29
Page80

Reference (36 of 126)
Citation Number967599
Document TypeJournal
AuthorsSkita; Meyer
CODENCHBEAM
Journal TitleChem.Ber.
(Series) Volume45
Publication Year1912
Page3586

Reference (37 of 126)
Citation Number967610
Document TypeJournal
AuthorsTunmann
CODENCHZEA6
Journal TitleChem.Zentralbl.
Language CodeGE
(Series) Volume89
NumberII
Publication Year1918
Page675

Reference (38 of 126)
Citation Number968116
Document TypeJournal
AuthorsPurvis
CODENJCSOA9
Journal TitleJ.Chem.Soc.
(Series) Volume103
Publication Year1913
Page2291

Reference (39 of 126)
Citation Number969748
Document TypeJournal
AuthorsWagenaar
CODENPHWEAW
Journal TitlePharm.Weekbl.
(Series) Volume66
Publication Year1929
Page405

Reference (40 of 126)
Citation Number969749
Document TypeJournal
AuthorsTammann
CODENZAACAB
Journal TitleZ.Anorg.Allg.Chem.
(Series) Volume181
Publication Year1929
Page413

Reference (41 of 126)
Citation Number969751
Document TypeJournal
AuthorsTammann; Hesse
CODENZAACAB
Journal TitleZ.Anorg.Allg.Chem.
(Series) Volume156
Publication Year1926
Page252

Reference (42 of 126)
Citation Number969752
Document TypeJournal
AuthorsTammann; Tampke
CODENZAACAB
Journal TitleZ.Anorg.Allg.Chem.
(Series) Volume162
Publication Year1927
Page10

Reference (43 of 126)
Citation Number969753
Document TypeJournal
AuthorsHasselblatt
CODENZAACAB
Journal TitleZ.Anorg.Allg.Chem.
(Series) Volume119
Publication Year1921
Page361

Reference (44 of 126)
Citation Number969754
Document TypeJournal
AuthorsTammann
CODENZEPCAC; ZAACAB
Journal TitleZ.Phys.Chem.Stoechiom.Verwandtschaftsl.; Z.Anorg.Allg.Chem.
(Series) Volume25; 181
Publication Year1894; 1929
Page450; 413

Reference (45 of 126)
Citation Number981382
Document TypeJournal
AuthorsSato
Journal/Review Without CODENJapan Analyst; Chem.Abstr.
(Series) Volume6
Publication Year1957; 1958
Page83; 16088

Reference (46 of 126)
Citation Number981383
Document TypeJournal
AuthorsHans; Santavy
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Reaction (1 of 31)
Reaction ID1746488
Reactant BRN4327482; 1310620
Reactant2-(3,6-diisopropyl-pyrazine-2-sulfinyl)-1-piperidin-1-yl-ethanone; 5-(3-bromo-1-propenyl)-1,3-dioxaindan
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Reagent1.) potassium diisopropylamide (KDA)
Other Conditions1.) THF, hexane, RT, 1 h, 2.) THF, hexane, reflux
CommentYield given. Multistep reaction
Citation Pointer5535863; Journal; Ohta, Akihiro; Tonomura, Yoshiko; Sawaki, Junko; Naohito, Sato; Akiike, Hitomi; et al.; HTCYAM; Heterocycles; EN; 32; 5; 1991; 965-973;

Reaction (2 of 31)
Reaction ID1748676
Reactant BRN1365055; 131691
ReactantN-2-butenoylpiperidine; benzo[1,3]dioxole-5-carbaldehyde
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details3
Reaction ClassificationChemical behaviour
Reagenttriethylbenzylammoniumchloride, 50percent KOH
Solventdimethylsulfoxide
Time2 hour(s)
Temperature60 - 65
Other Conditionsvarious solvents
Subject StudiedProduct distribution
Citation Pointer5623047; Journal; Schulze, Andreas; Oediger, Hermann; LACHDL; Liebigs Ann.Chem.; GE; 9; 1981; 1725-1727;

Reaction (3 of 31)
Reaction ID1839034
Reactant BRN167676; 4416084
Reactant1-benzo[1,3]dioxol-5-yl-allyl alcohol; 1-p-tolylsulfanylethynyl-piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Other Conditions1.) BF3OEt2 in refluxing toluene; 2.) oxidation (m-chloroperbenzoic acid, CH2Cl2,-78 grad C); 3.) reflux in toluene
CommentYield given. Multistep reaction
Citation Pointer5542826; Journal; Nakai, Takeshi; Setoi, Hiroyuki; Kageyama, Yasuhide; TELEAY; Tetrahedron Lett.; EN; 22; 41; 1981; 4097-4100;

Reaction (4 of 31)
Reaction ID2627935
Reactant BRN4613019
Reactantacetic acid 1-(benzenesulfonyl-benzo[1,3]dioxol-5-yl-methyl)-4-oxo-4-piperidin-1-yl-butyl ester
Product BRN90739; 90741
Product1-(5-benzo[1,3]dioxol-5-yl-penta-2,4-dienoyl)-piperidine; 1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Reagentt-BuOK
Solvent2-methyl-propan-2-ol
Time12 hour(s)
Other ConditionsAmbient temperature
CommentYield given. Yields of byproduct given
Citation Pointer5546680; Journal; Mandai, Tadakatsu; Moriyama, Tadashi; Tsujimoto, Koichiro; Kawada, Mikio; Otera, Junzo; TELEAY; Tetrahedron Lett.; EN; 27; 5; 1986; 603-606;

Reaction (5 of 31)
Reaction ID3829573
Reactant BRN85624; 102438
Reactanttrans,trans-piperinic acid; piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details2
Reaction ClassificationPreparation
Yield90 percent (BRN=90741)
ReagentN,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride, triethylamine
SolventCH2Cl2
Time60 min
Temperature20 - 25
Citation Pointer5571390; Journal; Cabre, Juan; Palomo, Antonio Luis; SYNTBF; Synthesis; EN; 5; 1984; 413-417;

Reaction (6 of 31)
Reaction ID3829578
Reactant BRN85625; 102438
Reactant5t-benzo[1,3]dioxol-5-yl-penta-2t,4-dienoyl chloride; piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details2
Reaction ClassificationPreparation
Solventdiethyl ether
Citation Pointer5576619; Journal; Banerji, Avijit; Ghosal, Tapasree; Acharyya, Aditi K.; IJSBDB; Indian J.Chem.Sect.B; EN; 23; 6; 1984; 546-549;

Reaction (7 of 31)
Reaction ID3863772
Reactant BRN1101343; 90741
Reactantchloromalonic acid diethyl ester; 1-trans,trans-piperinoyl-piperidine
Product BRN1805352; 4894122
Productethenetetracarboxylic acid tetraethyl ester; 3-benzo[1,3]dioxol-5-yl-6-(piperidine-1-carbonyl)-3,6-dihydro-selenopyran-2,2-dicarboxylic acid diethyl ester
No. of Reaction Details1
Reaction ClassificationPreparation
Yield24 percent (BRN=4894122); 70 percent (BRN=1805352)
Reagentselenium, Cs2CO3
Solventacetonitrile
Other ConditionsHeating
Citation Pointer5597332; Journal; Abelman, Matthew M.; TELEAY; Tetrahedron Lett.; EN; 32; 50; 1991; 7389-7392;

Reaction (8 of 31)
Reaction ID3863773
Reactant BRN1101343; 90741
Reactantchloromalonic acid diethyl ester; 1-trans,trans-piperinoyl-piperidine
Product BRN4894108
Product3-benzo[1,3]dioxol-5-yl-6-(piperidine-1-carbonyl)-3,6-dihydro-thiopyran-2,2-dicarboxylic acid diethyl ester
No. of Reaction Details1
Reaction ClassificationPreparation
Yield80 percent (BRN=4894108)
Reagentsulfur, Cs2CO3
Solventacetonitrile
Other ConditionsHeating
Citation Pointer5597332; Journal; Abelman, Matthew M.; TELEAY; Tetrahedron Lett.; EN; 32; 50; 1991; 7389-7392;

Reaction (9 of 31)
Reaction ID3863774
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN110253
Product1-nitroso-piperidine
No. of Reaction Details2
Reaction ClassificationPreparation
Yield2.36 percent (BRN=110253)
ReagentHClO4 (pH 3.0), NaNO2
SolventH2O
Time2 hour(s)
Temperature100
Citation Pointer5874363; Journal; Nakamura, Masamichi; Katoh, Kuni; Kawabata, Toshiharu; ABCHA6; Agric.Biol.Chem.; EN; 45; 5; 1981; 1257-1260;

Reaction (10 of 31)
Reaction ID3863775
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN288703
Product1-(5-benzo[1,3]dioxol-5-yl-pentanoyl)-piperidine
No. of Reaction Details4
Reaction ClassificationPreparation
ReagentH2
Catalyst10 percent Pd/C
Solventmethanol
Time2 hour(s)
Pressure2585.74
Reaction TypeCatalytic hydrogenation
Citation Pointer6262921; Journal; Ablordeppey, Seth Y.; Fischer, James B.; Glennon, Richard A.; BMECEP; Bioorg.Med.Chem.; EN; 8; 8; 2000; 2105 - 2112;

Reaction (11 of 31)
Reaction ID3863776
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN6144494; 6168367
ProductZ-5-benzylidene-(3,4-methylenedioxy)-2(5H)-furanone; E,E-piperylpiperidine dimer
No. of Reaction Details3
Reaction ClassificationChemical behaviour
Yield26 percent (BRN=6144494); 30 percent (BRN=6168367)
Reagentrose bengal
Solventmethanol
Time18 hour(s)
Other ConditionsIrradiation
Subject StudiedMechanism
Citation Pointer5753488; Journal; Kumar, Anil; Krupadanam, G L David; Srimannarayana, G; IJSBDB; Indian J.Chem.Sect.B; EN; 31; 11; 1992; 784-785;

Reaction (12 of 31)
Reaction ID3863777
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN6662570
Product4,5-(trans)-2,3-epoxy piperylpiperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Yield75 percent (BRN=6662570)
Reagent1percent H2O2
Time18 hour(s)
Temperature37
Other ConditionsHorseradish peroxidase, 0,1M sodium phosphate buffer, pH 6,5
Citation Pointer5851492; Journal; Rao, A. Bhaskar; Rao, M. Venkateswara; Kumar, Anil; Krupadanam, G. L. David; Srimannarayana, G.; TELEAY; Tetrahedron Lett.; EN; 35; 2; 1994; 279-280;

Reaction (13 of 31)
Reaction ID3863778
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN85624
Producttrans,trans-piperinic acid
No. of Reaction Details3
Reaction ClassificationPreparation
Reagent10percent ethanolic NaOH
Solventethanol
Citation Pointer5725528; Journal; Nakamura, Norio; Kiuchi, Fumiyuki; Tsuda, Yoshisuke; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2647-2651;

Reaction (14 of 31)
Reaction ID4925582
Reactant BRN7989620; 114442
Reactant5-(2-iodo-vinyl)-benzo[1,3]dioxole; 1-acryloyl-piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Yield38 percent (BRN=90741)
Reagentpalladium acetate, triphenylphosphine, lithium chloride, triethylamine
Solventacetonitrile
Time18 hour(s)
Temperature70 - 80
Citation Pointer6096589; Journal; Naskar, Dinabandhu; Chowdhury, Shantanu; Roy, Sujit; TELEAY; Tetrahedron Lett.; EN; 39; 7; 1998; 699-702;

Reaction (15 of 31)
Reaction ID4975527
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN8003486; 288703
Product5-benzo[1,3]dioxol-5-yl-1-piperidin-1-yl-pent-4-en-1-one; 1-(5-benzo[1,3]dioxol-5-yl-pentanoyl)-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Yield58 percent (BRN=288703); 14 percent (BRN=8003486)
ReagentNaBH4 (0.008 mole), I2 (0.003 mole)
Solventtetrahydrofuran
Time20 min
Temperature0
Citation Pointer6096582; Journal; Das, Biswanath; Kashinatham, A.; Madhusudhan, P.; TELEAY; Tetrahedron Lett.; EN; 39; 7; 1998; 677-678;

Reaction (16 of 31)
Reaction ID4975528
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN8003486
Product5-benzo[1,3]dioxol-5-yl-1-piperidin-1-yl-pent-4-en-1-one
No. of Reaction Details1
Reaction ClassificationPreparation
Yield74 percent (BRN=8003486)
ReagentNaBH4 (0.0025 mole), I2 (0.001 mole)
Solventtetrahydrofuran
Time20 min
Temperature0
Citation Pointer6096582; Journal; Das, Biswanath; Kashinatham, A.; Madhusudhan, P.; TELEAY; Tetrahedron Lett.; EN; 39; 7; 1998; 677-678;

Reaction (17 of 31)
Reaction ID5043968
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN8117956; 1261487
Product5-benzo[1,3]dioxol-5-yl-1-piperidin-1-yl-pent-3-en-1-one; trans-Db,g-Dihydro-piperidin
No. of Reaction Details1
Reaction ClassificationPreparation
Yield95 percent (BRN=1261487)
ReagentZn, HOAc
Time2 hour(s)
Other ConditionsAmbient temperature
Citation Pointer6117787; Journal; Das, Biswanath; Madhusudhan, P.; TELEAY; Tetrahedron Lett.; EN; 39; 49; 1998; 9099-9100;

Reaction (18 of 31)
Reaction ID5311563
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN1261487
Producttrans-Db,g-Dihydro-piperidin
No. of Reaction Details1
Reaction ClassificationPreparation
Yield96 percent (BRN=1261487)
ReagentMg; MeOH
Time2 hour(s)
Temperature20
Reaction TypeReduction
Citation Pointer6209404; Journal; Das, Biswanth; Kashinatham, A.; Venkataiah, B.; SYNCAV; Synth.Commun.; EN; 29; 21; 1999; 3799 - 3804;

Reaction (19 of 31)
Reaction ID5392515
Reactant BRN1238185; 90741
Reactantbenzophenone; 1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationChemical behaviour (half reaction)
Other Conditionsim Licht
CommentHandbook
Citation Pointer745868; Journal; Paterno; GCITA9; Gazz.Chim.Ital.; 44 II; 1914; 104, 106;

Reaction (20 of 31)
Reaction ID5680972
Reactant BRN90741; 1718733
Reactant1-trans,trans-piperinoyl-piperidine; ethanol; phenylmercury-acetate
Product BRN53813
Product1-[5t-(6-phenylmercurio-benzo[1,3]dioxol-5-yl)-penta-2t,4-dienoyl]-piperidine
No. of Reaction Details2
Reaction ClassificationPreparation
CommentHandbook
Citation Pointer784769; Patent; Lever Brothers Co.; US 2085064; 1935;

Reaction (21 of 31)
Reaction ID5709607
Reactant BRN90741
Reactantalcoholic KOH-solution; 1-trans,trans-piperinoyl-piperidine
Product BRN102438; 85624
Productpiperidine; trans,trans-piperinic acid
No. of Reaction Details1
Reaction ClassificationChemical behaviour
CommentHandbook
Citation Pointer960841; Journal; v. Babo; Keller; JPCEAO; J.Prakt.Chem.; <1> 72; 1857; 55; JCVWAE; Jahresber.Fortschr.Chem.Verw.Theile Anderer Wiss.; 1857; 413;503101; Journal; Fittig; Mielck; JLACBF; Justus Liebigs Ann. Chem.; 152; 1869; 52, 54; JLACBF; Justus Liebigs Ann. Chem.; 172; 1874; 140, 152;

Reaction (22 of 31)
Reaction ID5714786
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation (half reaction)
Citation Pointer3132215; Journal; Tsuboi; Takeda; TELEAY; Tetrahedron Lett.; 1979; 1043;3140982; Journal; Grewe et al.; CHBEAM; Chem.Ber.; 103; 1970; 3752,3766;3141492; Journal; Lurik et al.; PCJOAU; Pharm.Chem.J.(Engl.Transl.); 5; 8; 1971; 462; KHFZAN; Khim.Farm.Zh.; 5; 8; 1971; 15;2995721; Patent; Haarmann and Reimer; DE 2757506; 1977;

Reaction (23 of 31)
Reaction ID5714787
Reactant BRN102438
Reactantchavicinoyl chloride; piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
CommentHandbook
Citation Pointer520054; Journal; Lohaus; Gall; JLACBF; Justus Liebigs Ann. Chem.; 517; 1935; 278, 284;507531; Journal; Lohaus; JPCEAO; J.Prakt.Chem.; <2> 119; 1928; 258;

Reaction (24 of 31)
Reaction ID5714788
Reactant BRN102438
Reactantpiperidine; piperinic acid chloride
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Reagentbenzene
CommentHandbook
Citation Pointer960844; Journal; Ruegheimer; CHBEAM; Chem.Ber.; 15; 1882; 1391;

Reaction (25 of 31)
Reaction ID5746581
Reactant BRN1718733; 90741
Reactantethanol; hydrogen; colloidal palladium; 1-trans,trans-piperinoyl-piperidine
Producttetrahydropiperine
No. of Reaction Details1
Reaction ClassificationChemical behaviour (half reaction)
CommentHandbook
Citation Pointer505033; Journal; Borsche; CHBEAM; Chem.Ber.; 44; 1911; 2945;967599; Journal; Skita; Meyer; CHBEAM; Chem.Ber.; 45; 1912; 3586;1310037; Journal; Paal; CHBEAM; Chem.Ber.; 45; 1912; 2226;

Reaction (26 of 31)
Reaction ID5746582
Reactant BRN1098214; 90741
Reactanthydrogen; hydrochloric acid; palladium chloride; 1-trans,trans-piperinoyl-piperidine
Producttetrahydropiperine
No. of Reaction Details1
Reaction ClassificationChemical behaviour (half reaction)
CommentHandbook
Citation Pointer621663; Journal; Skita; Franck; CHBEAM; Chem.Ber.; 44; 1911; 2866;

Reaction (27 of 31)
Reaction ID5746583
Reactant BRN1098214; 90741
Reactanthydrogen; hydrochloric acid; platinum chlorides; 1-trans,trans-piperinoyl-piperidine
Producttetrahydropiperine
No. of Reaction Details1
Reaction ClassificationChemical behaviour (half reaction)
CommentHandbook
Citation Pointer621663; Journal; Skita; Franck; CHBEAM; Chem.Ber.; 44; 1911; 2866;

Reaction (28 of 31)
Reaction ID8539764
Reactant BRN84600; 114442
Reactant3-benzo[1,3]dioxol-5-yl-acrylic acid; 1-acryloyl-piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationMultistage
Yield51 percent (BRN=90741)
No. of Stages2
Stage 1
Stage 2
Stage Reactant BRN114442
Stage Reactant1-acryloyl-piperidine
ReagentN-bromosuccinimide; tetrabutylammonium trifluoroacetate; Pd(OAc)2; Ph3Sb; Et3N
Solvent1,2-dichloro-ethane; 1,2-dichloro-ethane
Time4 hour(s); 20 hour(s)
Temperature20
Reaction TypeDecarboxylation; bromination; Hunsdiecker reaction; Heck reaction
Citation Pointer6225104; Journal; Naskar, Dinabandhu; Roy, Sujit; TETRAB; Tetrahedron; EN; 56; 10; 2000; 1369 - 1378;

Reaction (29 of 31)
Reaction ID8735157
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN8705257
Product1-[1-(3,4-methylenedioxyphenyl)-2,4-pentadienyl]piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
ReagentLiAlH4
Solventdiethyl ether
Time24 hour(s)
Other ConditionsHeating
Reaction TypeReduction
Citation Pointer6262921; Journal; Ablordeppey, Seth Y.; Fischer, James B.; Glennon, Richard A.; BMECEP; Bioorg.Med.Chem.; EN; 8; 8; 2000; 2105 - 2112;

Reaction (30 of 31)
Reaction ID8900343
Reactant BRN7622; 2811397; 102438
Reactant3,4-methylenedioxy-trans-cinnamaldehyde; (triphenylphosphoranylidene)ethenone; piperidine
Product BRN90741
Product1-trans,trans-piperinoyl-piperidine
No. of Reaction Details1
Reaction ClassificationPreparation
Yield90 percent (BRN=90741)
Solventtetrahydrofuran
Time24 hour(s)
Other ConditionsHeating
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Reaction (31 of 31)
Reaction ID8986873
Reactant BRN90741
Reactant1-trans,trans-piperinoyl-piperidine
Product BRN8998762
Product(5-benzo[1,3]dioxol-5-yl-thiophen-2-yl)-piperidin-1-yl-methanone
No. of Reaction Details1
Reaction ClassificationPreparation
Yield23 percent (BRN=8998762)
Reagentnaphthalene-1,8-trisulfide-2-oxide
Solventchlorobenzene
Time16 hour(s)
Other ConditionsHeating
Citation Pointer6320341; Journal; Grainger, Richard S.; Procopio, Alberto; Steed, Jonathan W.; ORLEF7; Org.Lett.; EN; 3; 22; 2001; 3565 - 3568;

Isolation from Natural Product (1 of 30)
Isolation from Natural Productoleoresin, extract from fruits of Piper nigrum L. (Piperaceae)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Isolation from Natural Product (2 of 30)
Isolation from Natural Productstems of Piper tuberculatum
Citation Pointer6264052; Journal; Navickiene, Hosana Maria D.; Alecio, Alberto Camilo; Kato, Massuo Jorge; Bolzani, Vanderlan da S.; Young, Maria Claudia M.; Cavalheiro, Alberto Jose; Furlan, Maysa; PYTCAS; Phytochemistry; EN; 55; 2410; 2000; 621 - 626;

Isolation from Natural Product (3 of 30)
Isolation from Natural Productdry fruits of black pepper
Citation Pointer6225880; Journal; Paula, Vanderlucia F. de; A Barbosa, Luiz C. de; Demuner, Antonio J.; Pilo-Veloso, Dorila; Picanco, Marcelo C.; PMSCFC; Post Manage.Sci.; EN; 56; 2; 2000; 168 - 174;

Isolation from Natural Product (4 of 30)
Isolation from Natural Productfruits of Piper retrofractum Vahl.
Citation Pointer6205590; Journal; Pande, Archana; Shukla, Y. N.; Srivastava, Ritu; Verma, Monika; IJSBDB; Indian J.Chem.Sect.B; EN; 36; 4; 1997; 377 - 379;

Isolation from Natural Product (5 of 30)
Isolation from Natural Productthe fruits of Piper Longum Linn (Piperaceae)
Citation Pointer6161595; Journal; Das, B.; Kashinatham, A.; Madhusudhan, P.; BCFAAI; Boll.Chim.Farm.; EN; 137; 8; 1998; 319 - 320;

Isolation from Natural Product (6 of 30)
Isolation from Natural Productleaves of Piper betle
Citation Pointer6124808; Journal; Parmar, Virinder S.; Jain, Subhash C.; Gupta, Sangita; Talwar, Sangeeta; Rajwanshi, Vivek K.; et al.; PYTCAS; Phytochemistry; EN; 49; 4; 1998; 1069-1078;

Isolation from Natural Product (7 of 30)
Isolation from Natural Productstems and leaves of Piper khasiana, Piper thomsoni, Piper acutislegnum
Citation Pointer6124808; Journal; Parmar, Virinder S.; Jain, Subhash C.; Gupta, Sangita; Talwar, Sangeeta; Rajwanshi, Vivek K.; et al.; PYTCAS; Phytochemistry; EN; 49; 4; 1998; 1069-1078;

Isolation from Natural Product (8 of 30)
Isolation from Natural ProductPiper acutisleginum, Piperle, Piper khasiana
Citation Pointer6080863; Journal; Parmar, Virinder S.; Jain, Subhash C.; Bisht, Kirpal S.; Jain, Pajni; Taneja, Poonam; et al.; PYTCAS; Phytochemistry; EN; 46; 4; 1997; 597-674;

Isolation from Natural Product (9 of 30)
Isolation from Natural Productfruits of Piper nigrum
Citation Pointer6070238; Journal; Siddiqui, Bina S.; Begum, Sabira; Gulzar, Tahsin; Noor, Farhat and Fatima; PYTCAS; Phytochemistry; EN; 45; 8; 1997; 1617-1620;

Isolation from Natural Product (10 of 30)
Isolation from Natural Productfruits of Piper longum L. (Piperaceae), climber from India
Citation Pointer6049858; Journal; Das, Biswanath; Kashinatham, A.; Srinivas, K. V. N. S.; PLMEAA; Planta Med.; EN; 62; 6; 1996; 582;

Isolation from Natural Product (11 of 30)
Isolation from Natural Productblack pepper at 294 bar and 42 deg C, extracted with CO2
Citation Pointer5945187; Journal; Braumann, Urich; Haendel, heidrun; Albert, Klaus; Ecker, Rainer; Spraul, Manfred; ANCHAM; Anal.Chem.; EN; 67; 5; 1995; 930-935;

Isolation from Natural Product (12 of 30)
Isolation from Natural Productfruits of white pepper (Piper nigrum L.)
Citation Pointer5874394; Journal; Nakatani, Nobuji; Inatani, Reiko; ABCHA6; Agric.Biol.Chem.; EN; 45; 6; 1981; 1473-1476;

Isolation from Natural Product (13 of 30)
Isolation from Natural ProductPiper nigrum L.
Citation Pointer5874363; Journal; Nakamura, Masamichi; Katoh, Kuni; Kawabata, Toshiharu; ABCHA6; Agric.Biol.Chem.; EN; 45; 5; 1981; 1257-1260;

Isolation from Natural Product (14 of 30)
Isolation from Natural ProductUlocladium sp.
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;

Isolation from Natural Product (15 of 30)
Isolation from Natural Productfruits of Javanese long pepper, Piper retrofractum Vahl.
Citation Pointer5846053; Journal; Kikuzaki, Hiroe; Kawabata, Marona; Ishida, Etsuko; Akazawa, Yoko; Takei, Yoko; et al.; BBBIEJ; Biosci.Biotechnol.Biochem.; EN; 57; 8; 1993; 1329-1333;

Isolation from Natural Product (16 of 30)
Isolation from Natural ProductAnethum sowa (seeds)
Citation Pointer5749938; Journal; Jain, A. K.; Sharma, N. D.; Gupta, S. R.; IJSBDB; Indian J.Chem.Sect.B; EN; 25; 1986; 979;

Isolation from Natural Product (17 of 30)
Isolation from Natural Productpepper, fruits of Piper nigrum L.
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Isolation from Natural Product (18 of 30)
Isolation from Natural ProductPiper retrofractum (Piperaceae)
Citation Pointer5710925; Journal; Ahn, Jong-Woong; Ahn, Mi-Ja; Zee, Ok-Pyo; Kim, Eun-Joo; Lee, Sueg-Geun; et al.; PYTCAS; Phytochemistry; EN; 31; 10; 1992; 3609-3612;

Isolation from Natural Product (19 of 30)
Isolation from Natural Productfruits of Piper longum L.
Citation Pointer5673694; Journal; Tabuneng, Wnanbyr; Bando, Hideo; Amiya, Takashi; CPBTAL; Chem.Pharm.Bull.; EN; 31; 10; 1983; 3562-3565;

Isolation from Natural Product (20 of 30)
Isolation from Natural ProductPiper argyrophyllum Miq.
Citation Pointer5575872; Journal; Banerji, Avijit; Nandi, Gopa; IJSBDB; Indian J.Chem.Sect.B; EN; 27; 1-12; 1988; 163-165;

Isolation from Natural Product (21 of 30)
Isolation from Natural ProductPiper nigrum L.
Citation Pointer5510783; Journal; Das, B. P.; Jamal, Molla Yousuf; Choudhury, B.; JICSAH; J.Indian Chem.Soc.; EN; 67; 1; 1990; 72-73;

Isolation from Natural Product (22 of 30)
Isolation from Natural ProductVork. u. Isol. aus Piper peepuloides
Citation Pointer3143698; Journal; Dhar; Raina; PLMEAA; Planta Med.; 23; 1973; 295,296;

Isolation from Natural Product (23 of 30)
Isolation from Natural Productaus schwarzem Pfeffer
Citation Pointer3141492; Journal; Lurik et al.; PCJOAU; Pharm.Chem.J.(Engl.Transl.); 5; 8; 1971; 462; KHFZAN; Khim.Farm.Zh.; 5; 8; 1971; 15;

Isolation from Natural Product (24 of 30)
Isolation from Natural Productaus Papaver aurantiacum
Citation Pointer3132150; Journal; Madhusudhana et al.; CUSCAM; Curr.Sci.; 43; 1974; 76;

Isolation from Natural Product (25 of 30)
Isolation from Natural Productaus Fruechten von Piper guineense
Citation Pointer156361; Journal; Okogun,J.I.; Ekong,D.E.U.; JCPRB4; J.Chem.Soc.Perkin Trans.1; EN; 1974; 2195-2198;

Isolation from Natural Product (26 of 30)
Isolation from Natural ProductFindet sich in den unreifen Fruechten ('schwarzer Pfeffer') und in den Kernen der reifen Fruechte ('weisser Pfeffer') von Piper nigrum
CommentHandbook
Citation Pointer960850; Journal; Varrentrapp; Will; JLACBF; Justus Liebigs Ann. Chem.; 39; 1841; 283;960851; Journal; Regnault; ANCPAC; Ann.Chim.(Paris); <2> 68; 1838; 158;960852; Journal; Liebig; JLACBF; Justus Liebigs Ann. Chem.; 6; 1833; 36;960853; Journal; Pelletier; ANCPAC; Ann.Chim.(Paris); <2> 51; 1832; 199; JLACBF; Justus Liebigs Ann. Chem.; 6; 1833; 33;960854; Journal; Pelletier; ANCPAC; Ann.Chim.(Paris); <2> 16; 1821; 344; Schw.; 32; 436;960855; Journal; Oerstedt; Schweiggers Journ. f. Chemie u. Physik; 29; 80;

Isolation from Natural Product (27 of 30)
Isolation from Natural ProductFindet sich ferner im langen Pfeffer (reife Fruechte von P. longum und P. officinarum)
CommentHandbook
Citation Pointer960848; Journal; Wangerin; Pharm. Ztg.; 48; 454;960849; Journal; Bauer; Hilger; CHZEA6; Chem.Zentralbl.; GE; 67; I; 1896; 1214;

Isolation from Natural Product (28 of 30)
Isolation from Natural Productin den Fruechten von P. Clusii (Aschantipfeffer)
CommentHandbook
Citation Pointer960846; Journal; Herlant; PHJOAV; Pharm.J.; <3> 25; 643;960847; Journal; Stenhouse; PHJOAV; Pharm.J.; <1> 14; 363; JLACBF; Justus Liebigs Ann. Chem.; 95; 1855; 106;

Isolation from Natural Product (29 of 30)
Isolation from Natural Productin der Wurzelrinde von Artanthe geniculata (unechte Jaborandi)
CommentHandbook
Citation Pointer960845; Journal; Peckolt; Apoth. Ztg.; 10; 471;

Isolation from Natural Product (30 of 30)
Isolation from Natural Productin den Fruechten von P. Lowong
CommentHandbook
Citation Pointer502948; Journal; Peinemann; ARPMAS; Arch.Pharm.(Weinheim Ger.); 234; 1896; 258;

Derivative (1 of 1)
Derivative BRN288703
Derivative1-(5-benzo[1,3]dioxol-5-yl-pentanoyl)-piperidine
Citation Pointer5749938; Journal; Jain, A. K.; Sharma, N. D.; Gupta, S. R.; IJSBDB; Indian J.Chem.Sect.B; EN; 25; 1986; 979;

Related Structure (1 of 1)
Citation Pointer3635101; Journal; De Cleyn; Verzele; BSCBAG; Bull.Soc.Chim.Belg.; 84; 1975; 435,436;

Crossfile Reference (1 of 4)
NamePiperine, purum
Crossfile SourceFluka
External Access ID80810

Crossfile Reference (2 of 4)
NamePiperidine, 1-<5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl>-, (E,E)-
Crossfile SourceCRC Handbook of Chemistry and Physics
External Access ID20134

Crossfile Reference (3 of 4)
Data Type13C-NMR Spectrum
Crossfile SourceCSEARCH
External Access IDSADT-12317

Crossfile Reference (4 of 4)
Data Type13C-NMR Spectrum
Crossfile SourceCSEARCH
External Access IDUNIW-14585

Crystal Property Description (1 of 2)
Colour & Other Propertieslight-yellow
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Crystal Property Description (2 of 2)
Colour & Other PropertiesPrismen
CommentHandbook
Citation Pointer967610; Journal; Tunmann; CHZEA6; Chem.Zentralbl.; GE; 89; II; 1918; 675;

Melting Point (1 of 19)
Solventethyl acetate
CommentHandbook
Citation Pointer967610; Journal; Tunmann; CHZEA6; Chem.Zentralbl.; GE; 89; II; 1918; 675;

Melting Point (2 of 19)
Melting Point131
Solventdiethyl ether
Citation Pointer5749938; Journal; Jain, A. K.; Sharma, N. D.; Gupta, S. R.; IJSBDB; Indian J.Chem.Sect.B; EN; 25; 1986; 979;

Melting Point (3 of 19)
Melting Point132
Solventbenzene
Citation Pointer3132150; Journal; Madhusudhana et al.; CUSCAM; Curr.Sci.; 43; 1974; 76;

Melting Point (4 of 19)
Melting Point130
Citation Pointer5575872; Journal; Banerji, Avijit; Nandi, Gopa; IJSBDB; Indian J.Chem.Sect.B; EN; 27; 1-12; 1988; 163-165;

Melting Point (5 of 19)
Melting Point130
Citation Pointer3143698; Journal; Dhar; Raina; PLMEAA; Planta Med.; 23; 1973; 295,296;

Melting Point (6 of 19)
Melting Point129.5
CommentHandbook
Citation Pointer502948; Journal; Peinemann; ARPMAS; Arch.Pharm.(Weinheim Ger.); 234; 1896; 258;

Melting Point (7 of 19)
Melting Point129.5
CommentHandbook
Citation Pointer981397; Journal; Kofler,L.u.A.; Thermo-Mikro-Methoden,3.Aufl.; <Weinheim 1954> S.471;

Melting Point (8 of 19)
Melting Point127
Citation Pointer5975360; Journal; Dehmlow, Eckehard V.; Shamout, Abdul Rahman; JRMPDM; J.Chem.Res.Miniprint; GE; 4; 1981; 1178-1184;

Melting Point (9 of 19)
Melting Point129
Citation Pointer5874394; Journal; Nakatani, Nobuji; Inatani, Reiko; ABCHA6; Agric.Biol.Chem.; EN; 45; 6; 1981; 1473-1476;

Melting Point (10 of 19)
Melting Point128
Citation Pointer5576619; Journal; Banerji, Avijit; Ghosal, Tapasree; Acharyya, Aditi K.; IJSBDB; Indian J.Chem.Sect.B; EN; 23; 6; 1984; 546-549;

Melting Point (11 of 19)
Melting Point129
Citation Pointer3143025; Journal; Patra; Gosh; PYTCAS; Phytochemistry; 13; 1974; 2889;3635101; Journal; De Cleyn; Verzele; BSCBAG; Bull.Soc.Chim.Belg.; 84; 1975; 435,436;

Melting Point (12 of 19)
Melting Point128
Citation Pointer3140982; Journal; Grewe et al.; CHBEAM; Chem.Ber.; 103; 1970; 3752,3766;

Melting Point (13 of 19)
Melting Point128.5 - 130
Citation Pointer3714671; Journal; Meerov; Katyuzhanskaya; CHNCA8; Chem.Nat.Compd.(Engl.Transl.); 9; 1973; 179; KPSUAR; Khim.Prir.Soedin.; 9; 1973; 184;

Melting Point (14 of 19)
Melting Point129 - 130
Citation Pointer2995721; Patent; Haarmann and Reimer; DE 2757506; 1977;

Melting Point (15 of 19)
Melting Point128 - 129.5
Citation Pointer3141492; Journal; Lurik et al.; PCJOAU; Pharm.Chem.J.(Engl.Transl.); 5; 8; 1971; 462; KHFZAN; Khim.Farm.Zh.; 5; 8; 1971; 15;

Melting Point (16 of 19)
Melting Point128 - 130
Citation Pointer156361; Journal; Okogun,J.I.; Ekong,D.E.U.; JCPRB4; J.Chem.Soc.Perkin Trans.1; EN; 1974; 2195-2198;

Melting Point (17 of 19)
Melting Point128 - 129.5
CommentHandbook
Citation Pointer960844; Journal; Ruegheimer; CHBEAM; Chem.Ber.; 15; 1882; 1391;

Melting Point (18 of 19)
Melting Point128 - 129
Citation Pointer6070238; Journal; Siddiqui, Bina S.; Begum, Sabira; Gulzar, Tahsin; Noor, Farhat and Fatima; PYTCAS; Phytochemistry; EN; 45; 8; 1997; 1617-1620;

Melting Point (19 of 19)
Melting Point124
Citation Pointer6205590; Journal; Pande, Archana; Shukla, Y. N.; Srivastava, Ritu; Verma, Monika; IJSBDB; Indian J.Chem.Sect.B; EN; 36; 4; 1997; 377 - 379;

Crystal Phase (1 of 8)
DescriptionRate of crystallization
Commentvon unterkuehltem Piperin bei verschiedenen Temperaturen.; Handbook
Citation Pointer969754; Journal; Tammann; ZEPCAC; Z.Phys.Chem.Stoechiom.Verwandtschaftsl.; 25; 1894; 450; ZAACAB; Z.Anorg.Allg.Chem.; 181; 1929; 413;

Crystal Phase (2 of 8)
DescriptionRate of crystallization
Commentvon unterkuehltem Piperidin bei Drucken bis 1000 kg/cm2.; Handbook
Citation Pointer969753; Journal; Hasselblatt; ZAACAB; Z.Anorg.Allg.Chem.; 119; 1921; 361;

Crystal Phase (3 of 8)
DescriptionRate of crystallization
CommentGeschwindigkeit der Bildung von Keimen bei der Kristallisation von unterkuehlten Schmelzen bei 20grad bzw. bei 48grad:.; Handbook
Citation Pointer981393; Journal; Kondoguri; ZETFA7; Zh.Eksp.Teor.Fiz.; 11; 1941; 728; Chem.Abstr.; 1943; 1314;2200674; Journal; Michnewitsch; KOZHAG; Kolloidn.Zh.; 21; 1959; 69; engl. Ausg. S. 61;

Crystal Phase (4 of 8)
DescriptionRate of crystallization
CommentKeimbildung bei der Kristallisation von unterkuehlten Schmelzen in Abhaengigkeit von der Temperatur (72-80grad):.; Handbook
Citation Pointer2175033; Journal; Tammann; Elsner v. Gronow; ZAACAB; Z.Anorg.Allg.Chem.; 200; 1931; 57, 68;

Crystal Phase (5 of 8)
DescriptionRate of crystallization
Commentin Abhaengigkeit von der Temperatur(0gradbis 90grad) und vom Reinheitsgrad:.; Handbook
Citation Pointer981393; Journal; Kondoguri; ZETFA7; Zh.Eksp.Teor.Fiz.; 11; 1941; 728; Chem.Abstr.; 1943; 1314;

Crystal Phase (6 of 8)
DescriptionRate of crystallization
CommentVerstaerkte Keimbildung bei der Kristallisation von unterkuehlten Schmelzen bei Einwirkung von Ultraschall.; Handbook
Citation Pointer2175021; Journal; Danilow; Tewerowskii; ZETFA7; Zh.Eksp.Teor.Fiz.; 10; 1940; 1305, 1308; Chem.Abstr.; 1941; 5368;

Crystal Phase (7 of 8)
DescriptionInterplanar spacing
Commentvon kristallinem und von fluessigem Piperin:.; Handbook
Citation Pointer981396; Journal; Lewaschewitsch et al.; Trudy Dnetropetrovsk.chim.-technol.Inst.; 4; 1955; 84,88; Chem.Abstr.; 1959; 9760;

Crystal Phase (8 of 8)
DescriptionSolid state structure properties
Citation Pointer3132105; Journal; Grynpas; Lindley; ACBCAR; Acta Crystallogr.Sect.B; 31; 1975; 2663,2664,2665,2666;

Sublimation (1 of 1)
Sublimation104
Pressure0.02
CommentHandbook
Citation Pointer636409; Journal; Janot; Chaigneau; COREAF; C.R.Hebd.Seances Acad.Sci.; 225; 1947; 1371;

Density of the Liquid (1 of 4)
Density of the Liquid1.25
Commentg/cm**3
Citation Pointer3132105; Journal; Grynpas; Lindley; ACBCAR; Acta Crystallogr.Sect.B; 31; 1975; 2663,2664,2665,2666;

Density of the Liquid (2 of 4)
Density of the Liquid1.192
Reference Temperature4
Measurement Temperature20
CommentHandbook
Citation Pointer981390; Journal; Kordes; ZPCBAL; Z.Phys.Chem.Abt.B; 43; 1939; 173,186;

Density of the Liquid (3 of 4)
Density of the Liquid1.13
Measurement Temperature113
Commentg/cm**3; Handbook
Citation Pointer969752; Journal; Tammann; Tampke; ZAACAB; Z.Anorg.Allg.Chem.; 162; 1927; 10;

Density of the Liquid (4 of 4)
Density of the Liquid1.12
Measurement Temperature136
Commentg/cm**3; Handbook
Citation Pointer969752; Journal; Tammann; Tampke; ZAACAB; Z.Anorg.Allg.Chem.; 162; 1927; 10;

Dynamic Viscosity (1 of 1)
Dynamic Viscosity11.3
Temperature95
CommentHandbook
Citation Pointer969749; Journal; Tammann; ZAACAB; Z.Anorg.Allg.Chem.; 181; 1929; 413;969752; Journal; Tammann; Tampke; ZAACAB; Z.Anorg.Allg.Chem.; 162; 1927; 10;969751; Journal; Tammann; Hesse; ZAACAB; Z.Anorg.Allg.Chem.; 156; 1926; 252;

Refractive Index (1 of 1)
Refractive Index1.6846
Wavelength589
Temperature20
CommentHandbook
Citation Pointer981390; Journal; Kordes; ZPCBAL; Z.Phys.Chem.Abt.B; 43; 1939; 173,186;

Nuclear Magnetic Resonance (1 of 15)
Coupling Nuclei1H-1H
SolventsCDCl3
Frequency500
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Nuclear Magnetic Resonance (2 of 15)
DescriptionSpectrum
Nucleus1H
Temperature41.9
Citation Pointer5945187; Journal; Braumann, Urich; Haendel, heidrun; Albert, Klaus; Ecker, Rainer; Spraul, Manfred; ANCHAM; Anal.Chem.; EN; 67; 5; 1995; 930-935;

Nuclear Magnetic Resonance (3 of 15)
DescriptionChemical shifts
Nucleus13C
SolventsCDCl3
Frequency125.7
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Nuclear Magnetic Resonance (4 of 15)
DescriptionChemical shifts
Nucleus1H
SolventsCDCl3
Frequency500
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Nuclear Magnetic Resonance (5 of 15)
DescriptionChemical shifts
Nucleus1H
SolventsCDCl3
Citation Pointer6090513; Journal; Abarbri, Mohamed; Parrain, Jean-Luc; Duchene, Alain; SYNCAV; Synth.Commun.; EN; 28; 2; 1998; 239-250;

Nuclear Magnetic Resonance (6 of 15)
DescriptionChemical shifts
Nucleus13C
SolventsCDCl3
Citation Pointer6090513; Journal; Abarbri, Mohamed; Parrain, Jean-Luc; Duchene, Alain; SYNCAV; Synth.Commun.; EN; 28; 2; 1998; 239-250;

Nuclear Magnetic Resonance (7 of 15)
DescriptionChemical shifts
Nucleus1H
SolventsCDCl3
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;

Nuclear Magnetic Resonance (8 of 15)
DescriptionChemical shifts
Nucleus13C
SolventsCDCl3
Citation Pointer5787666; Journal; Banerji, Avijit; Sarkar, Manjusha (nee Chaudhuri); Ghosal, Tapasree; Pal, Sudhir Chandra; ORMRBD; Org.Magn.Reson.; EN; 22; 11; 1984; 734-736;

Nuclear Magnetic Resonance (9 of 15)
DescriptionChemical shifts
Nucleus1H
SolventsCDCl3
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Nuclear Magnetic Resonance (10 of 15)
DescriptionChemical shifts
Nucleus13C
SolventsCDCl3
Citation Pointer5576619; Journal; Banerji, Avijit; Ghosal, Tapasree; Acharyya, Aditi K.; IJSBDB; Indian J.Chem.Sect.B; EN; 23; 6; 1984; 546-549;5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Nuclear Magnetic Resonance (11 of 15)
Description2D-NMR
Citation Pointer5945187; Journal; Braumann, Urich; Haendel, heidrun; Albert, Klaus; Ecker, Rainer; Spraul, Manfred; ANCHAM; Anal.Chem.; EN; 67; 5; 1995; 930-935;

Nuclear Magnetic Resonance (12 of 15)
DescriptionNMR
Citation Pointer3143025; Journal; Patra; Gosh; PYTCAS; Phytochemistry; 13; 1974; 2889;3633754; Journal; Wenkert et al.; JACSAT; J.Amer.Chem.Soc.; 93; 1971; 6271;3635101; Journal; De Cleyn; Verzele; BSCBAG; Bull.Soc.Chim.Belg.; 84; 1975; 435,436;

Nuclear Magnetic Resonance (13 of 15)
DescriptionSpin-spin coupling constants
SolventsCDCl3
Comment1H-1H
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;6090513; Journal; Abarbri, Mohamed; Parrain, Jean-Luc; Duchene, Alain; SYNCAV; Synth.Commun.; EN; 28; 2; 1998; 239-250;

Nuclear Magnetic Resonance (14 of 15)
DescriptionSpin-spin coupling constants
SolventsCDCl3
Comment1H-13C.
Citation Pointer5787666; Journal; Banerji, Avijit; Sarkar, Manjusha (nee Chaudhuri); Ghosal, Tapasree; Pal, Sudhir Chandra; ORMRBD; Org.Magn.Reson.; EN; 22; 11; 1984; 734-736;

Nuclear Magnetic Resonance (15 of 15)
DescriptionSpin-spin coupling constants
SolventsCDCl3
Comment1H-1H
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Infrared Spectra (1 of 12)
DescriptionBands
SolventKBr
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Infrared Spectra (2 of 12)
DescriptionBands
Comment3058 - 1043 cm**(-1)
Citation Pointer6090513; Journal; Abarbri, Mohamed; Parrain, Jean-Luc; Duchene, Alain; SYNCAV; Synth.Commun.; EN; 28; 2; 1998; 239-250;

Infrared Spectra (3 of 12)
DescriptionBands
Comment1650 - 930 cm**(-1)
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;

Infrared Spectra (4 of 12)
DescriptionBands
SolventKBr
Comment1635 - 925 cm**(-1)
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Infrared Spectra (5 of 12)
DescriptionBands
SolventCHCl3
Comment1635 - 1585 cm**(-1)
Citation Pointer5725528; Journal; Nakamura, Norio; Kiuchi, Fumiyuki; Tsuda, Yoshisuke; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2647-2651;

Infrared Spectra (6 of 12)
DescriptionBands
SolventKBr
Comment1635 - 1585 cm**(-1)
Citation Pointer5725528; Journal; Nakamura, Norio; Kiuchi, Fumiyuki; Tsuda, Yoshisuke; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2647-2651;

Infrared Spectra (7 of 12)
DescriptionBands
SolventKBr
Comment1641 - 1624 cm**(-1)
Citation Pointer5571390; Journal; Cabre, Juan; Palomo, Antonio Luis; SYNTBF; Synthesis; EN; 5; 1984; 413-417;

Infrared Spectra (8 of 12)
DescriptionBands
Solventnujol
Comment1600 - 780 cm**(-1); Handbook
Citation Pointer642911; Journal; Pleat et al.; JPHAA3; J.Am.Pharm.Assoc.; 40; 1951; 107, 108;

Infrared Spectra (9 of 12)
DescriptionBands
SolventKBr
Comment3020 - 710 cm**(-1); Handbook
Citation Pointer511899; Journal; Briggs et al.; ANCHAM; Anal.Chem.; 29; 1957; 904, 905;

Infrared Spectra (10 of 12)
DescriptionBands
SolventCHCl3
Comment1635 - 1580 cm**(-1); Handbook
Citation Pointer511899; Journal; Briggs et al.; ANCHAM; Anal.Chem.; 29; 1957; 904, 905;1056240; Journal; Marion et al.; JACSAT; J.Amer.Chem.Soc.; 73; 1951; 305,; JACSAT; J.Amer.Chem.Soc.; 74; 1952; 270;

Infrared Spectra (11 of 12)
DescriptionBands
SolventCHCl3
Comment1490 - 930 cm**(-1); Handbook
Citation Pointer511899; Journal; Briggs et al.; ANCHAM; Anal.Chem.; 29; 1957; 904, 905;1056240; Journal; Marion et al.; JACSAT; J.Amer.Chem.Soc.; 73; 1951; 305,; JACSAT; J.Amer.Chem.Soc.; 74; 1952; 270;

Infrared Spectra (12 of 12)
DescriptionIR
Citation Pointer3132150; Journal; Madhusudhana et al.; CUSCAM; Curr.Sci.; 43; 1974; 76;3143025; Journal; Patra; Gosh; PYTCAS; Phytochemistry; 13; 1974; 2889;

Ultraviolet Spectra (1 of 10)
DescriptionSpectrum
SolventCHCl3
Comment300 - 400 nm; Handbook
Citation Pointer981386; Journal; Tausig et al.; JFOTAP; J.Food Technol.; 10; 1956; 151;

Ultraviolet Spectra (2 of 10)
DescriptionSpectrum
Solventethanol
Comment290 - 380 nm; Handbook
Citation Pointer529237; Journal; Spring; Stark; JCSOA9; J.Chem.Soc.; 1950; 1177, 1178;

Ultraviolet Spectra (3 of 10)
DescriptionAbsorption maxima
Absorption Maxima341
Ext./Abs. Coefficient20893
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;

Ultraviolet Spectra (4 of 10)
DescriptionAbsorption maxima
Solventmethanol
Absorption Maxima309; 341
Citation Pointer5749938; Journal; Jain, A. K.; Sharma, N. D.; Gupta, S. R.; IJSBDB; Indian J.Chem.Sect.B; EN; 25; 1986; 979;

Ultraviolet Spectra (5 of 10)
DescriptionAbsorption maxima
Solventmethanol
Absorption Maxima343
Ext./Abs. Coefficient34700
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Ultraviolet Spectra (6 of 10)
DescriptionAbsorption maxima
Solventmethanol
Absorption Maxima245; 255; 262; 311
Ext./Abs. Coefficient11100; 11200; 11100; 21700
Citation Pointer5729448; Journal; Kiuchi, Fumiyuki; Nakamura, Norio; Tsuda, Yoshisuke; Kondo, Kaoru; Yoshimura, Hiroyuki; CPBTAL; Chem.Pharm.Bull.; EN; 36; 7; 1988; 2452-2465;

Ultraviolet Spectra (7 of 10)
DescriptionAbsorption maxima
Citation Pointer3635101; Journal; De Cleyn; Verzele; BSCBAG; Bull.Soc.Chim.Belg.; 84; 1975; 435,436;

Ultraviolet Spectra (8 of 10)
DescriptionAbsorption maxima
Commentdes Dampfes.; Handbook
Citation Pointer968116; Journal; Purvis; JCSOA9; J.Chem.Soc.; 103; 1913; 2291;

Ultraviolet Spectra (9 of 10)
DescriptionAbsorption maxima
Solventethanol
CommentHandbook
Citation Pointer505581; Journal; Dobbie; Fox; JCSOA9; J.Chem.Soc.; 103; 1913; 1194;

Ultraviolet Spectra (10 of 10)
DescriptionUV/VIS
Citation Pointer3132150; Journal; Madhusudhana et al.; CUSCAM; Curr.Sci.; 43; 1974; 76;3140982; Journal; Grewe et al.; CHBEAM; Chem.Ber.; 103; 1970; 3752,3766;3141492; Journal; Lurik et al.; PCJOAU; Pharm.Chem.J.(Engl.Transl.); 5; 8; 1971; 462; KHFZAN; Khim.Farm.Zh.; 5; 8; 1971; 15;3143025; Journal; Patra; Gosh; PYTCAS; Phytochemistry; 13; 1974; 2889;3714671; Journal; Meerov; Katyuzhanskaya; CHNCA8; Chem.Nat.Compd.(Engl.Transl.); 9; 1973; 179; KPSUAR; Khim.Prir.Soedin.; 9; 1973; 184;

Mass Spectrum (1 of 5)
Citation Pointer3140982; Journal; Grewe et al.; CHBEAM; Chem.Ber.; 103; 1970; 3752,3766;3635101; Journal; De Cleyn; Verzele; BSCBAG; Bull.Soc.Chim.Belg.; 84; 1975; 435,436;

Mass Spectrum (2 of 5)
Descriptionspectrum; electron impact (EI)
Citation Pointer6311443; Journal; Schobert, Rainer; Siegfried, Sven; Gordon, Gary J.; JCSPCE; J.Chem.Soc.Perkin Trans.1; EN; 19; 2001; 2393 - 2397;

Mass Spectrum (3 of 5)
Descriptionspectrum
Citation Pointer5864041; Journal; Dahiya, Jagroop S.; Woods, Donald L.; Tewari, Jalpa P.; PYTCAS; Phytochemistry; EN; 27; 7; 1988; 2366;6090513; Journal; Abarbri, Mohamed; Parrain, Jean-Luc; Duchene, Alain; SYNCAV; Synth.Commun.; EN; 28; 2; 1998; 239-250;

Mass Spectrum (4 of 5)
Descriptionspectrum; electron impact (EI)
Citation Pointer5825902; Journal; Semler, Ursula; Gross, Georg G.; PYTCAS; Phytochemistry; EN; 27; 5; 1988; 1566-1568;

Mass Spectrum (5 of 5)
Descriptionelectron impact (EI)
Citation Pointer5874363; Journal; Nakamura, Masamichi; Katoh, Kuni; Kawabata, Toshiharu; ABCHA6; Agric.Biol.Chem.; EN; 45; 5; 1981; 1257-1260;

Electrical Data (1 of 1)
DescriptionPiezoelectricity
CommentHandbook
Citation Pointer536898; Journal; Kopzik et al.; VMUNAE; Vestn.Mosk.Univ.; 13; 6; 1958; 91, 94; Chem.Abstr.; 1959; 15673;

Dissociation Exponent (1 of 3)
Dissociation Exponent (pK)14
Temperature18
Methodconductometric
Typeapparent
CommentHandbook
Citation Pointer625734; Journal; v. Weisse; Meyer-Levy; JCPBAN; J.Chim.Phys.Phys.Chim.Biol.; 14; 1916; 276; CHZEA6; Chem.Zentralbl.; GE; 87; II; 1916; 1030;

Dissociation Exponent (2 of 3)
Dissociation Exponent (pK)12.22
Temperature18
Typeb/thermodynamic
CommentHandbook
Citation Pointer740972; Journal; Kolthoff; BIZEA2; Biochem.Z.; 162; 1925; 340; PHJOAV; Pharm.J.; 118; 126; CHZEA6; Chem.Zentralbl.; GE; 98; I; 1927; 2116;

Dissociation Exponent (3 of 3)
Dissociation Exponent (pK)11.72
Temperature55
Typeb/thermodynamic
CommentHandbook
Citation Pointer625129; Journal; Arnall; JCSOA9; J.Chem.Soc.; 117; 1920; 837;

Electrochemical Characteristics (1 of 1)
Descriptionpolarographic current/voltage curve
CommentHandbook
Citation Pointer981382; Journal; Sato; Japan Analyst; 6; 1957; 83; Chem.Abstr.; 1958; 16088;981383; Journal; Hans; Santavy; C.csl.Lekarn.; 59; 1946; 40; Chem.Abstr.; 1948; 3504;

Solubility (MCS) (1 of 8)
Temperature15
Solventtrichloroethene
CommentSolubility :9.83 %.; Handbook
Citation Pointer559145; Journal; Wester; CHZEA6; Chem.Zentralbl.; GE; 86; I; 1915; 248;

Solubility (MCS) (2 of 8)
Solventaq. pyridine
CommentSolubility :11 %.at:20-25 degreeC.; Handbook
Citation Pointer505376; Journal; Dehn; JACSAT; J.Amer.Chem.Soc.; 39; 1917; 1400;

Solubility (MCS) (3 of 8)
Solventpyridine
CommentSolubility :23 %.; Handbook
Citation Pointer505376; Journal; Dehn; JACSAT; J.Amer.Chem.Soc.; 39; 1917; 1400;

Solubility (MCS) (4 of 8)
Solventethanol
Comment1 part(s) of substance.dissolves in:30 parts of solvent.; Handbook
Citation Pointer969748; Journal; Wagenaar; PHWEAW; Pharm.Weekbl.; 66; 1929; 405;

Solubility (MCS) (5 of 8)
Solventethanol
Comment1 part(s) of substance.dissolves in:1 parts of solvent.in boiling solvent.; Handbook
Citation Pointer969748; Journal; Wagenaar; PHWEAW; Pharm.Weekbl.; 66; 1929; 405;

Solubility (MCS) (6 of 8)
Solventethanol
Comment 100 g solvent dissolves. 6.66 g Substance.at:20-25 degreeC.; Handbook
Citation Pointer562634; Journal; Pucher; Dehn; JACSAT; J.Amer.Chem.Soc.; 43; 1921; 1755;

Solubility (MCS) (7 of 8)
Solubility0.04
Saturationin solution
Temperature18
SolventH2O
CommentHandbook
Citation Pointer740972; Journal; Kolthoff; BIZEA2; Biochem.Z.; 162; 1925; 340; PHJOAV; Pharm.J.; 118; 126; CHZEA6; Chem.Zentralbl.; GE; 98; I; 1927; 2116;

Solubility (MCS) (8 of 8)
Solubility0.4
Saturationin solution
Temperature18
Solventaq. HCl
CommentHandbook
Citation Pointer740972; Journal; Kolthoff; BIZEA2; Biochem.Z.; 162; 1925; 340; PHJOAV; Pharm.J.; 118; 126; CHZEA6; Chem.Zentralbl.; GE; 98; I; 1927; 2116;

Boundary Surface Phenomena (MCS) (1 of 1)
DescriptionSurface tension
SolventH2O
CommentHandbook
Citation Pointer625737; Journal; Zeehuisen; AEPPAE; Naunyn-Schmiedeberg's Arch.Exp.Pathol.Pharmakol.; 86; 1920; 366; CHZEA6; Chem.Zentralbl.; GE; 91; III; 1920; 668;

Pharmacological Data (1 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (2 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (3 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (4 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (5 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (6 of 60)
Citation Pointer6318024; Journal; Sunkara, G.; Mada, S. R.; Vobalaboina, V.; PHARAT; Pharmazie; EN; 56; 8; 2001; 640 - 642;

Pharmacological Data (7 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (8 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (9 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (10 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (11 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (12 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (13 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (14 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (15 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (16 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (17 of 60)
Citation Pointer6303601; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 3; 2001; 284 - 287;

Pharmacological Data (18 of 60)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Pharmacological Data (19 of 60)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Pharmacological Data (20 of 60)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Pharmacological Data (21 of 60)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Pharmacological Data (22 of 60)
Citation Pointer6303567; Journal; Bajad, Sunil; Bedi, K. L.; Singla, A. K.; Johri, R. K.; PLMEAA; Planta Med.; EN; 67; 2; 2001; 176 - 179;

Pharmacological Data (23 of 60)
Citation Pointer6264052; Journal; Navickiene, Hosana Maria D.; Alecio, Alberto Camilo; Kato, Massuo Jorge; Bolzani, Vanderlan da S.; Young, Maria Claudia M.; Cavalheiro, Alberto Jose; Furlan, Maysa; PYTCAS; Phytochemistry; EN; 55; 2410; 2000; 621 - 626;

Pharmacological Data (24 of 60)
CommentNo effect
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (25 of 60)
CommentNo effect
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (26 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (27 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (28 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (29 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (30 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (31 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (32 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (33 of 60)
Citation Pointer6261759; Journal; Rauscher, Frederick M.; Sanders, Ruth A.; Watkins, John B.; JBMTFQ; J.Biochem.Mol.Toxicol.; EN; 14; 6; 2000; 329 - 334;

Pharmacological Data (34 of 60)
Citation Pointer6235546; Journal; Daware, Mahadeo B.; Mujumdar, Arvind M.; Ghaskadbi, Surendra; PLMEAA; Planta Med.; EN; 66; 3; 2000; 231 - 236;

Pharmacological Data (35 of 60)
Citation Pointer6235546; Journal; Daware, Mahadeo B.; Mujumdar, Arvind M.; Ghaskadbi, Surendra; PLMEAA; Planta Med.; EN; 66; 3; 2000; 231 - 236;

Pharmacological Data (36 of 60)
Citation Pointer6235546; Journal; Daware, Mahadeo B.; Mujumdar, Arvind M.; Ghaskadbi, Surendra; PLMEAA; Planta Med.; EN; 66; 3; 2000; 231 - 236;

Pharmacological Data (37 of 60)
Citation Pointer6235546; Journal; Daware, Mahadeo B.; Mujumdar, Arvind M.; Ghaskadbi, Surendra; PLMEAA; Planta Med.; EN; 66; 3; 2000; 231 - 236;

Pharmacological Data (38 of 60)
Citation Pointer6235546; Journal; Daware, Mahadeo B.; Mujumdar, Arvind M.; Ghaskadbi, Surendra; PLMEAA; Planta Med.; EN; 66; 3; 2000; 231 - 236;

Pharmacological Data (39 of 60)
Citation Pointer6224648; Journal; Koul, Surrinder; Koul, Jawahir L.; Taneja, Subhash C.; Dhar, Kanaya L.; Jamwal, Deshvir S.; Singh, Kuldeep; Reen, Rashmeet K.; Singh, Jaswant; BMECEP; Bioorg.Med.Chem.; EN; 8; 1; 2000; 251 - 268;

Pharmacological Data (40 of 60)
Citation Pointer6224648; Journal; Koul, Surrinder; Koul, Jawahir L.; Taneja, Subhash C.; Dhar, Kanaya L.; Jamwal, Deshvir S.; Singh, Kuldeep; Reen, Rashmeet K.; Singh, Jaswant; BMECEP; Bioorg.Med.Chem.; EN; 8; 1; 2000; 251 - 268;

Pharmacological Data (41 of 60)
Citation Pointer6224648; Journal; Koul, Surrinder; Koul, Jawahir L.; Taneja, Subhash C.; Dhar, Kanaya L.; Jamwal, Deshvir S.; Singh, Kuldeep; Reen, Rashmeet K.; Singh, Jaswant; BMECEP; Bioorg.Med.Chem.; EN; 8; 1; 2000; 251 - 268;

Pharmacological Data (42 of 60)
Citation Pointer6224648; Journal; Koul, Surrinder; Koul, Jawahir L.; Taneja, Subhash C.; Dhar, Kanaya L.; Jamwal, Deshvir S.; Singh, Kuldeep; Reen, Rashmeet K.; Singh, Jaswant; BMECEP; Bioorg.Med.Chem.; EN; 8; 1; 2000; 251 - 268;

Pharmacological Data (43 of 60)
Citation Pointer6224648; Journal; Koul, Surrinder; Koul, Jawahir L.; Taneja, Subhash C.; Dhar, Kanaya L.; Jamwal, Deshvir S.; Singh, Kuldeep; Reen, Rashmeet K.; Singh, Jaswant; BMECEP; Bioorg.Med.Chem.; EN; 8; 1; 2000; 251 - 268;

Pharmacological Data (44 of 60)
Citation Pointer6221629; Journal; Kuenzi, Frederick M.; Dale, Nicholas; BJPCBM; Br.J.Pharmacol.; EN; 119; 1; 1996; 81 - 90;

Pharmacological Data (45 of 60)
Citation Pointer6202145; Journal; Chu, C.- Y.; Chang, J.-P.; Wang, C.-J.; FCTOD7; Food Chem.Toxicol.; EN; 32; 4; 1994; 373 - 378;

Pharmacological Data (46 of 60)
Citation Pointer6202145; Journal; Chu, C.- Y.; Chang, J.-P.; Wang, C.-J.; FCTOD7; Food Chem.Toxicol.; EN; 32; 4; 1994; 373 - 378;

Pharmacological Data (47 of 60)
Citation Pointer6199610; Journal; Kang, Min Hee; Won, Sun Me; Park, Sang Shin; Kim, Sang Geon; Novak, R. F.; Kim, Nak Doo; XENOBH; Xenobiotica; EN; 24; 12; 1994; 1195 - 1204;

Pharmacological Data (48 of 60)
Citation Pointer6188824; Journal; Unchern, Surachai; Saito, Hiroshi; Nishiyama, Nobuyoshi; BPBLEO; Biol.Pharm.Bull.; EN; 20; 9; 1997; 958 - 961;

Pharmacological Data (49 of 60)
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (50 of 60)
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (51 of 60)
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (52 of 60)
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (53 of 60)
CommentNo effect
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (54 of 60)
CommentNo effect
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (55 of 60)
CommentNo effect
Citation Pointer6143346; Journal; Wink, M.; Schmeller, T.; Latz-Bruening, B; JCECD8; J.Chem.Ecol.; EN; 24; 11; 1998; 1881 - 1938;

Pharmacological Data (56 of 60)
Citation Pointer6132209; Journal; Singh, Amar; Sharma, S. C.; Zutshi, Usha; Bedi, K. L.; PHSCFB; Pharm.Sci.; EN; 3; 4; 1997; 189 - 192;

Pharmacological Data (57 of 60)
Commentin vitro anti-invasive activity against MCF-7/6 cells: anti-invasive at a dose 100 mM, not anti-invasive at a dose 1 mM and 10 mM
Citation Pointer6073861; Journal; Parmar, Virinder S.; Bracke, Marc E.; Philippe, Jan; Wengel, Jesper; Jain, Subhash C.; et al.; BMECEP; Bioorg.Med.Chem.; EN; 5; 8; 1997; 1609-1620;

Pharmacological Data (58 of 60)
Commentno effect on the induction of histidine revertants in Salmonella typhimurium in 10 - 500 nmol/plate; no mutagenic effect in the bone marrow micronucleus test in Swiss mice in 10 - 20 mg/kg dose; did not induce any aberration in the sperm cells
Citation Pointer6061215; Journal; Karekar, Varsha R.; Mujumdar, Arvind M.; Joshi, Savita S.; Dhuley, Jayant; Shinde, Sambhaji L.; Ghaskadbi, Surendra; ARZNAD; Arzneim.Forsch.; EN; 46; 10; 1996; 972-975;

Pharmacological Data (59 of 60)
Commentno insecticidal activity against Callosobruchus chinensis L.
Citation Pointer5942128; Journal; Miyakado, Masakazu; Nakayama, Isamu; Yoshioka, Hirosuke; ABCHA6; Agric.Biol.Chem.; EN; 44; 7; 1980; 1701-1704;

Pharmacological Data (60 of 60)
Commenttoxicity to mosquito larvae (Culex Spp.); LC50
Citation Pointer5510783; Journal; Das, B. P.; Jamal, Molla Yousuf; Choudhury, B.; JICSAH; J.Indian Chem.Soc.; EN; 67; 1; 1990; 72-73;