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1. |
Phenylpropanoid Glycoside Esters: Leucine Aminopeptidase Inhibitors fromHebe strictavar.Atkinsonii |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 87-94
StephenJ. Kellam,
KevinA. Mitchell,
JohnW. Blunt,
BruceM. Clark,
MurrayH.G. Munro,
JohnR.L. Walker,
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摘要:
Screening of New Zealand native plants for inhibitors of leucine aminopeptidase led to the isolation of a new phenylpropanoid glycoside ester, 2-O-caffeoyl-D-glucopyranose (1) fromHebe strictavar.atkinsonii(Scrophulariaceae). (1) is a competitive inhibitor of leucine aminopeptidase (Kj=10.5 μM). Two other compounds isolated, 3-methyl-3-(6′-O-caffeoyl-β-D-glucopyranosyloxy)-pentan-5-olide (2) and forsythiaside, 3′″, 4′″-dihydroxy-β-phenethyl-O-α-L-rhamnopyranosyl-(1′ → 6)-4-O-caffeoyl-β-D-glucopyranoside (3), were also shown to be competitive inhibitors with Kjvalues of 3.75 and 8.C μM respectively.
ISSN:1057-5634
DOI:10.1080/10575639308043843
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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2. |
The Structure of a New Ionone Glucoside from Starfruit (Averrhoa carambolaL.) |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 95-99
Andrea Lutz,
Peter Winterhalter,
Peter Schreier,
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摘要:
The 2-0-β-D-glucopyranoside of 4-(1′,4′-dihydroxy-2′,2′,6′-trimethylcyclohexyl)-but-3-en-2-ol1awas isolated from the juice ofAverrhoa carambolaby XAD-2 adsorption and MeOH elution. After a preseparation of the crude glycosidic extract with multi-layer coil countercurrent chromatography the new natural product was peracetylated, purified by HPLC and characterized as its pentaacetate1b.
ISSN:1057-5634
DOI:10.1080/10575639308043844
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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3. |
Phomenins A and B, Bioactive Polypropionate Pyrones from Culture Fluids ofPhoma tracheiphila |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 101-106
Corrado Tringali,
Agatina Parisi,
Mario Piattelli,
GaetanoMagnano di San Lio,
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摘要:
Two previously unreported polypropionate α-pyrones, phomenin A (2) and B (3), were isolated from culture fluids of the phytopathogenic fungusPhoma tracheiphila, and their structures elucidated essentially by spectroscopic methods. Phomenin A shows phytotoxic activity. Both phomenins A and B are active againstArtemia salina.
ISSN:1057-5634
DOI:10.1080/10575639308043845
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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4. |
Alkaloid Formation in Hairy Roots and Cell Suspensions ofRauwolfia serpentinaBenth |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 107-112
Heike Falkenhagen,
InnaN. Kuzovkina,
IrinaE. Alterman,
LubovA. Nikolaeva,
Joachim Stöckigt,
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摘要:
Growth and alkaloid formation of hairy roots ofRauwolfia serpentinaandRauwolfia vomitoriawere compared with that of well established cell suspension cultures ofRauwolfia serpentinaand differentiated plants. Cell suspensions revealed clearly better growth - twice of the dry weight observed for the root culture. The hairy roots do not produce the major indole alkaloids typical for the root bark ofRauwolfiaplants and synthesize besides vinorine and perakine two of the alkaloids formed in cell suspensions (vomilenine and ajmaline). The total yield of alkaloids of the cell culture is about 3.6-fold higher as compared with the root culture.
ISSN:1057-5634
DOI:10.1080/10575639308043846
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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5. |
Sponge Fatty Acids-4. Co-occurrence of Two Isoprenoid Fatty Acids (4,8,12-Trimethyltridecanoic and 5,9,13-Trimethyltetradecanoic) in Phospholipids of Marine Sponges from the GenusCinachrella |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 113-118
Gilles Barnathan,
Joseph Miralles,
Jean-Michel Kornprobst,
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摘要:
Two isoprenoid fatty acids, 4,8,12-trimethyltridecanoic and 5,9,13-trimethyltetradecanoic, were identified in all specimens studied of the Senegalese spongesCinachyrella allocladaandC. kükenthaliand the New-Caledonian spongeCinachyrellaaff.schulzei. The fatty acids were identified as methyl esters or N-acyl pyrrolidides by gas chromatography/mass spectrometry analyses. 4,8,12-Trimethyltridecanoic acid was found to be the major component in all Senegalese sponge fatty acid mixtures(up to 36%). The co-occurrence of these isoprenoid acids may have implications for chemotaxonomy and biosynthetic pathways.
ISSN:1057-5634
DOI:10.1080/10575639308043847
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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6. |
A Novel C-Methyl Isoflavone fromAbronia latifolia |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 119-122
Eckhard Wollenweber,
Sabine Papendieck,
Gerhard Schilling,
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摘要:
Leaves and stems ofAbronia latifolia(Nyctaginaceae) are covered with a sticky material containing several flavonoid aglycones. In addition to some common flavones and flavonols, this exudate contains a novel C-methylated isoflavone (1), named abronisoflavone. This is the first report of the occurrence of an isoflavone in this family.
ISSN:1057-5634
DOI:10.1080/10575639308043848
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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7. |
Microbial Hydroxylation of 24-Epicastasterone by the FungusCochliobolus lunatus |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 123-129
Brunhilde Voigt,
Andrea Porzel,
Katrin Undisz,
Cläre Hörhold-Schubert,
Günter Adam,
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摘要:
24-Epicastasterone, a naturally occurring phytohormone of the brassinosteroid type, was transformed by the fungusCochliobolus lunatusto give the corresponding 15β-hydroxylated compound. The structure of this fermentation product was determined by spectroscopic methods, especially NMR investigations.
ISSN:1057-5634
DOI:10.1080/10575639308043849
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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8. |
Buxapapillosin - A New Triterpene from the Roots ofBuxus papillosa |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 131-138
Atta-ur-rahman,
Habib Nasir,
S.Safdar Ali,
Zahida Iqbal,
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摘要:
A newseco-triterpene, buxapapillosin (1) in which ring A has undergone cleavage, has been isolated from the roots ofBuxus papillosa. The compound bears a cyclopropane ring found in manyBuxusalkaloids and is therefore of biogenetic significance. The leaves ofBuxus papillosahave also yielded three known alkaloids, buxamine A, cyclomicrobuxamine and cyclomicrobuxinine, isolated for the first time from this plant.
ISSN:1057-5634
DOI:10.1080/10575639308043850
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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9. |
Bufadienolides and a Steroidal Sapogenin fromUrginea sanguinea(Hyacynthaceae) |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 139-143
Liselotte Krenn,
Brigitte Kopp,
Maria Bamberger,
Eva Brustmann,
Wolfgang Kubelka,
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摘要:
During investigations of the active principle ofUrginea sanguineaSchinz eight bufadienolides, a steroidal sapogenin and stigmasterol were isolated. The compounds were identified by FAB-MS,1H-NMR- and13C-NMR-studies or comparison with authentic substances as scillirosidin (1), desacetylscillirosidin (2), 12β-hydroxy-scillirosidin (3), 12β-hydroxy-desacetyl-scillirosidin (4), 12β-hydroxy-scilliroside (5), 5α-4,5-dihydro-12β-hydroxy-scillirosidin (6), 12β-hydroxy-scillirosidin-3-one (7), 12β-hydroxy-scilli-rubrosidin-3-one (8) and 7β, 15α-dihydroxy-yamogenin (9). The latter is the first steroidal sapogenin isolated from anUrgineaspecies.
ISSN:1057-5634
DOI:10.1080/10575639308043851
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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10. |
Further Compounds fromHaplophyllum ptilostylum |
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Natural Product Letters,
Volume 3,
Issue 2,
1993,
Page 145-147
Ayhan Ulubelen,
AliH. Meriçli,
Filiz Meriçli,
Nur Tan,
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摘要:
In addition to previously isolated coumarins and lignans, we have isolated a new coumarin, ptilin and two known lignans, matairesinol and arctigenin from the aerial parts ofHaplophyllum ptilostylum.
ISSN:1057-5634
DOI:10.1080/10575639308043852
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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