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1. |
Glabcensin Q-U, Five Newent-Kaurane Diterpenoids fromIsodon angustifoliusVar.Glabrescens |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 77-86
Qin-Shi Zhao,
Bei Jiang,
Jia Wang,
Zhong-Wen Lin,
Han-Dong Sun,
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摘要:
Examination of the diterpenoid constituents of the dried leaves ofIsodon angustifoliusvar.glabrescensled to the isolation of five newent-kaurane diterpenoids, named as glabcensin Q-U (2–6). The structures were elucidated on the basis of spectroscopic evidences.
ISSN:1028-6020
DOI:10.1080/10286029808039847
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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2. |
Two New Diterpenoid Alkaloids, Beiwusines A and B, fromAconitum kusnezoffii |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 87-92
Zheng-Bang Li,
Feng-Peng Wang,
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摘要:
Two new atisine-type diterpenoid alkaloids, beiwusine A (1) and B (2), have been isolated from the roots ofAconitum kusnezoffiiReichb. Their structures were established on the basis of spectroscopic data. Beiwusines A and B are the first examples of atisine-type diterpenoid alkaloids having a hydroxyl group at C-1. In addition, one known diterpenoid alkaloid spiramine H (3) has been isolated.
ISSN:1028-6020
DOI:10.1080/10286029808039848
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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3. |
A New Saponin from the Leaves and Stems ofPanax quinquefoliumL. Collected in Canada |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 93-97
Jinhui Wang,
Wen Li,
Xian Li,
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摘要:
A new dammarane-type saponin named quinquenoside L3 (1) together with vina-ginsenoside R3 (2) were isolated from the leaves and stems ofPanax quinquefoliumL. collected in Canada. On the basis of physicochemical and spectral evidences,1was established as 3-O-β-D-glucopyranosyl-20-O-[β-D-xylopyranosyl-(1 → 6)-β-D-glucopyranosyl] 20(S)-dammar-23-ene-3β, 12β,20,25-tetryol.
ISSN:1028-6020
DOI:10.1080/10286029808039849
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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4. |
Biotransformation of Podophyllotoxin to Picropodophyllin by Microbes |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 99-102
HongZhu Guo,
DeAn Guo,
XueYan Fei,
YaJun Cui,
JunHua Zheng,
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摘要:
Biotransformation of podophyllotoxin (PT) by several microbial species has been investigated. Among the fungi tested, it was found thatPenicilliumstrains can isomerize PT to picropodophyllin (PPT) in 8% yield and other strains also transform the substrate into the same product but with lower yield.
ISSN:1028-6020
DOI:10.1080/10286029808039850
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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5. |
New Iridoids fromPedicularis artselaeri |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 103-109
Bao-Ning Su,
Jian-Jun Zhai,
Zhong-Jian Jia,
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摘要:
Three new iridoids, named artselaenin I, II and III, were isolated from the whole plants ofPedicularis artselaeri, along with 11 known compounds, 8-epiloganic acid, 7-deoxy-8-epiloganic acid, plantarenaloside, mussaenoside, lariciresinol-4-O-β-D-glucoside, lariciresinol-4′-O-β-D-gluco-side, alaschaniosideA, cirtusinA, 2-(p-hydroxyphenyl)-ethanol 1-O-β-D-glucopyranoside, 3-methoxy-4-primeverosylacetophenone and adenine. Their structures were identified mainly by spectral evidence.
ISSN:1028-6020
DOI:10.1080/10286029808039851
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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6. |
Glucosylation of Salicyl Alcohol by Cell Suspension Cultures ofSolanum Laciniatum |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 111-117
Achmad Syahrani,
Ivy Widjaja,
Gunawan Indrayanto,
AlistairL. Wilkins,
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摘要:
Cell suspension cultures ofSolanum laciniatumwere able to transform exogenously inoculated salicyl alcohol into salicyl alcohol 7-O-β-D-glucopyranoside (isosalicin). The highest level of isosalicin (54.6 mg/g dry weight) in the cells was formed within 2 days after inoculation with salicyl alcohol (37.5 mg/flask containing 50ml of medium). The biotransformation capacity of the cell suspension cultures was about 31.1%.
ISSN:1028-6020
DOI:10.1080/10286029808039852
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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7. |
Studies on Dammarane-Type Saponins in the Flower-Buds ofPanax ginsengC.A. Meyer |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 119-123
Feng Qiu,
ZhongZe Ma,
Suixu Xu,
XinSheng Yao,
YingJie Chen,
ZhenTao Che,
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摘要:
From the dried flower-buds ofPanax ginsengC.A. Meyer, a new minor dammarane-type triterpene saponin named ginsenoside III together with nine known saponins was isolated. On the basis of spectral and chemical evidence, the structure of the new saponin was elucidated as 3-O-[β-D-glucopyranosyl(1 → 2)-β-D-glucopyranosyl]-20-O-β-D-glucopyranosyl-3β,12β,20(S)-trihydroxy-dammar-25-en-24-one.
ISSN:1028-6020
DOI:10.1080/10286029808039853
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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8. |
Lignans fromKadsura angustifolia |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 125-131
Ye-Gao Chen,
Guo-Wei Qin,
Yu-Yuan Xie,
Kin-Fai Cheng,
Zhong-Wen Lin,
Han-Dong Sun,
Young-Hwa Kang,
Byung-Hoon Han,
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摘要:
A new dibenzocyclooctadiene lignan named angustifolin D (1) together with four known lignans: kadsulignan L (2), kadsulignan N (3), schisantherin P (4) and meso-dihydroguaiaretic acid (5) were isolated from the stems ofKadsura angustifolia. Their structures and stereochemistries were elucidated by spectral studies. Compounds2and5showed moderate plateletactivating factor (PAF) antagonistic activities with IC50values of 2.6 × 10−5and 4.1 × 10−5M, respectively.
ISSN:1028-6020
DOI:10.1080/10286029808039854
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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9. |
A New Flavone 2′-Glucoside fromAndrographis alata |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 133-138
A.G. Damu,
B. Jayaprakasam,
D. Gunasekar,
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摘要:
A new flavone glucoside, 5,2′,6′-trihydroxy-7-methoxyflavone 2′-O-β-D-glucopyranoside has been isolated from the whole plant ofAndrographis alata. The structure was elucidated on the basis of spectral and chemical evidence.
ISSN:1028-6020
DOI:10.1080/10286029808039855
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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10. |
A New Bio-Active Flavonol Glycoside from the Stems ofButea superbaRoxb |
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Journal of Asian Natural Products Research,
Volume 1,
Issue 2,
1998,
Page 139-145
R.N. Yadava,
K.I. S. Reddy,
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摘要:
A new bio-active flavonol glycoside was isolated from the stems ofButea superbaRoxb, and its structure was determined by spectral analysis and chemical degradations as 3,5,7,3′,4′-pentahydroxy-8-methoxy-flavonol-3-O-β-D-xylopyranosyl(1 → 2)-α-L-rhamnopyranoside. The compound1showed antimicrobial activity against plant pathogenic fungiTrich viride, Asprgillus fumigatus, A. niger, A. terreus, Penicillium expansum, Helmitnhosporium oryzae, Botxitis cinerea, Rhizopus oligosporus, R. chinensis, Kelbsiella pneumoniae, Fusearium moniliformeand grampositive bacteriaStreplococcus pyogenes, Staphylococcus aureus, Bacillus subtilisgram-negative bacteriaEscherichia coli, Proteus vulgaris, Klebsiella pneumoniae, Pseudomonas aeruginosa. The maximum inhibitory effect was shown byH. oryzae, A. niger, B. cineraand gram-positive bacteria.
ISSN:1028-6020
DOI:10.1080/10286029808039856
出版商:Taylor & Francis Group
年代:1998
数据来源: Taylor
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