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1. |
Stratioside II - a C13 Norterpene Glucoside fromPistia stratiotes |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 83-86
MarinaDella Greca,
Antonio Fiorentino,
Pietro Monaco,
Lucio Previtera,
Armando Zarrelli,
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摘要:
The structure (3S,5R,6R,7E,9R)-3,5,6-trihydroxy-β-ionyl-3-O-β-D-glucopyranoside has been attributed to stratioside II, a component of the methanolic extract ofPistia stratiotes, on the basis of its spectroscopic features and by chemical correlation.
ISSN:1057-5634
DOI:10.1080/10575639608043244
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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2. |
Biotransformation of Lignans: Metabolism of (+)-Yangabin inSpodoptera litura |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 87-88
Mitsuo Miyazawa,
Hiroyuki Kasahara,
Hiromu Kameoka,
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摘要:
Biotransformation of (+)-yangabin inSpodoptera lituralarvae has been investigated. (+)-De-4′-O-methylyangabin-4′-O-β-D-glucoside were identified from the faeces of (+)-yangabin-administered larvae. The metabolic reaction of (+)-yangabin inSpodoptera lituralarvae is de-O-methylation atpara-position on the 3,4,5-trimethoxyl group followed by glucosidation.
ISSN:1057-5634
DOI:10.1080/10575639608043245
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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3. |
Annotemoyin-1 and -2: Two Novel Monotetrahydrofuranic γ-Lactone Acetogenins from the Seeds ofAnnona atemoya |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 89-95
P. Duret,
A.-I. Waechter,
R. Hocquemiller,
A. Cavé,
D. Batten,
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摘要:
Two new C35acetogenins belonging to the A1type (one tetrahydrofuran ring and an unsaturated γ-lactone) annotemoyin-1 (1) and annotemoyin-2 (2) have been isolated from the cytotoxic methanolic extract ofAnnona atemoyaseeds and have been identified as structural isomers of solamin (5). Their structures were established on the basis of NMR spectroscopic techniques. In addition two previously reported acetogenins, uvariamicin-III (3) and reticulatain-1 (4) which are new to this species were obtained.
ISSN:1057-5634
DOI:10.1080/10575639608043246
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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4. |
Triterpenes fromAcacia Dealbata |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 97-103
FlorbelaB. M. Pereira,
FernandoM. J. Domingues,
ArturM. S. Silva,
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摘要:
From the leaves, flowers and seeds ofA. dealbatafour lupene type triterpenes, lupenone, lupeol, lupenyl palpimate and lupenyl cinnamate, not previously reported in this genus, have been isolated. Their structures were established by spectroscopic means and by comparison with literature references.
ISSN:1057-5634
DOI:10.1080/10575639608043247
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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5. |
Elaeocarpidine Alkaloids fromPelargoniumSpecies (Geraniaceae) |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 105-112
MariaLis Balchin,
PeterJ Houghton,
TibebeZ. Woldemariam,
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摘要:
Three alkaloids, two of which could be fully characterised and were identified as elaeocarpidine1and epielaeocarpidine2, were isolated from leaves ofPelargoniumcultivar Appleblossom'. The structures were determined by means of UV, IR, Mass and NMR spectroscopy. This is the first report of alkaloids from the Geraniaceae.
ISSN:1057-5634
DOI:10.1080/10575639608043248
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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6. |
Epimerization of Taxol® in Human Cancer Cells |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 113-117
Hiroki Hamada,
Kazumi Sanada,
Shogo Ikeda,
Tazuko Oda,
HowardJ. Williams,
Guillermo Moyna,
A.Ian Scott,
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摘要:
Incubation of Jurkat T cells in solutions containing the anti-tumor agent taxol® produced a taxol® derivative with longer retention time on reverse phase HPLC, which was identified using NMR and mass spectroscopy as 7-epi-taxol, a product which is also found when taxol® is treated with base. No epimerization occurs in absence of cells. Epimerization may be explained by abnormally high pH inside cancer cells, and taxol would be expected to lose activity quickly after treatment due to the lower anti-tumor activity of the isomer formed.
ISSN:1057-5634
DOI:10.1080/10575639608043249
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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7. |
New Saponins fromMussaenda pubescens |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 119-126
Wei-Min Zhao,
Gen-Jin Yang,
Ren-Sheng Xu,
Guo-Wei Qin,
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摘要:
Two new saponins named mussaendoside I (1) and J (2) were isolated from the aerial parts ofMussaenda pubescensAit.f. On the basis of chemical and spectral methods, including 2D NMR technique, their structures were elucidated as 3-O-β-D-glucopyranosyl(1→2)-O-β-D-glucopyranosyl pomolic acid 28-O-β-D-glucopyranosyl ester and 3β-O-α-L-rhamnopyranosyl(1→2)-O-β-D-glucopyranosyl oleanolic acid 28-O-β-D-glucopyranosyl ester, respectively.
ISSN:1057-5634
DOI:10.1080/10575639608043250
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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8. |
Phenolics fromClematis chinensis |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 127-132
Bao-Ping Shao,
Ping Wang,
Guo-Wei Qin,
Ren-Sheng Xu,
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摘要:
From the aerial parts ofClematis chinensisa new pyranocoumarin named clematichinenol has been isolated and identified by spectroscopic methods. In addition, three known phenolics, (+)-syringaresinol, (-)-syringaresinol-4′-O-β-D-glucoside, acacetin-7-α-L-rhamnopyranosyl-(1-6)-β-D-glucopyranoside, and a lactone, digiprolactone were reported in the plant for the first time
ISSN:1057-5634
DOI:10.1080/10575639608043251
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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9. |
HIV-Inhibitory Gallotannins fromLepidobotrys staudtii |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 133-136
HeidiR. Bokesch,
TawnyaC. McKee,
MichaelJ. Currens,
RobertJ. Gulakowski,
JamesB. McMahon,
JohnH. Cardellina,
MichaelR. Boyd,
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摘要:
Three galloylquinic acids, 1,3,4,5-tetra-O-galloylquinic acid (1), 3,4,5-tri-O-galloylquinic acid (2), and methyl 3,4,5-tri-O-galloylquinate (3) were isolated from the stem bark of the monotypic plantLepidobotrys staudtii. Compound1protected target cells from the cytopathic effects of HIV-1 and HIV-2 and also exhibited potent inhibition of cellular DNA polymerases, as well as of the reverse transcriptases of HIV-1 and HIV-2, but not of other retroviruses tested.
ISSN:1057-5634
DOI:10.1080/10575639608043252
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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10. |
5′-Hydroxymethyl Cytomycin, a New Nucleoside Antibiotic fromStreptomyces sp.HKI-0052 |
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Natural Product Letters,
Volume 8,
Issue 2,
1996,
Page 137-144
T. Neumann,
W. Ihn,
M. Ritzau,
R. Vettermann,
W.F. Fleck,
U. Gräfe,
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摘要:
Streptomyces spec.HKI-0052 produces cytomycin (IIa) and the new 5′-hydroxymethylcytomycin (IIb) in addition to blasticidin S (Ia) and 5′-hydroxymethyl blasticidin S (Ib). The structure of the hithero unknown cytosine nucleoside IIb was settled by electrospray CID-MS/MS mass spectrometrical investigations.
ISSN:1057-5634
DOI:10.1080/10575639608043253
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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