Cytotoxic constituents from Podocarpus fasciculus (Q39996531)

16 September 2017

title

Cytotoxic constituents from Podocarpus fasciculus (English)

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

16 September 2017

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Podocarpus fasciculus

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16-Hydroxycommunic Acid

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kaempferol 7-O-glucoside

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(2R,3S)-2-(2,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol

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Kaempferol-7-o-glucoside

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

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hypolaetin-8-glucoside

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1,2,3,4-tetrahydroxybenzene

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(1R,4aS,10aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

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apigenin 7,4'-dimethyl ether

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(1S,4aS,10aR)-7-hydroxy-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

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(1S,2R,4R,5S,6R,9S,10R,17R)-5,10-dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione

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5-hydroxy-8-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenyl]-7-methoxy-2-(4-methoxyphenyl)chromen-4-one

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(1S,2S,4R,5R,6R,9S,10R,17R)-5,10-dihydroxy-1,6-dimethyl-12-propan-2-yl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-11,15-diene-7,14-dione

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Podocarpa-8,11,13-trien-19-oic acid

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3-Hydroxy-4-methoxybenzenepropanol

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

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(2S)-7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

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(1S,4aS,5S,8aR)-5-[(2Z)-3-(hydroxymethyl)penta-2,4-dienyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid

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2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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Podocarpus macrophyllus

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Podocarpus latifolius

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Podocarpus cunninghamii

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Podocarpus purdieanus

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Dacrycarpus imbricatus

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Yu-Jen Kuo

1

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16 September 2017

Shy-Yuan Hwang

2

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16 September 2017

Ming-Der Wu

3

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16 September 2017

Chia-Ching Liao

4

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16 September 2017

Yu-Han Liang

5

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16 September 2017

Yao-Haur Kuo

6

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16 September 2017

Hsiu-O Ho

7

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16 September 2017

language of work or name

English

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Chemical & Pharmaceutical Bulletin

publication date

2008

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Crossref

full work available at URL

16 September 2022

https://www.jstage.jst.go.jp/article/cpb/56/4/56_4_585/_pdf

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19 March 2024

https://api.unpaywall.org/v2/10.1248/cpb.56.585?email=unpaywall_01@example.com

published in

Chemical & Pharmaceutical Bulletin

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16 September 2017

volume

56

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16 September 2017

issue

4

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16 September 2017

page(s)

585-588

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https://api.unpaywall.org/v2/10.1248/cpb.56.585?email=unpaywall_01@example.com

16 September 2017

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19 March 2024

access restriction status

open access

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based on heuristic

inferred from online access status

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Nagilactones from Podocarpus nagi and Their Effects on the Feeding and Growth of Tobacco Budworm

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Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae).

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Diterpenoids from isodon flavidus

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Stable isotope labeling pattern of resveratrol and related natural stilbenes

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New sucrose phenylpropanoid esters from Polygonum perfoliatum

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Flavonol glycosides and novel iridoid glycoside from the leaves of Morinda citrifolia

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Revised structures for pluviatilol, methyl pluviatilol and xanthoxylol

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Methylated flavonols in the genus Gossypium

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Separation and identification of phenolic compounds in olive oil by coupling high-performance liquid chromatography with postcolumn solid-phase extraction to nuclear magnetic resonance spectroscopy (LC-SPE-NMR).

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Nitrification inhibitors from the roots of Leucaena leucocephala

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Podolide, a new antileukemic norditerpene dilactone fromPodocarpus gracilior

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Urinary metabolites of genistein administered orally to rats

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Abietane diterpenes from Illicium angustisepalum

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A bisnorditerpene dilactone from Podocarpus nagi

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Distribution and functions of norditerpene dilactones in Podocarpus species

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STUDY ON THE CHEMICAL SHIFTS FOR THE METHYL GROUPS OF DEOXYPODOCARPIC ACID (ENANTIOMER) TYPE COMPOUNDS AND SYNTHESES OF THEIR 10-BETA-15 OR 10-ALPHA-17 EPOXY DERIVATIVES

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Deoxygenation of polyhydroxybenzenes: an alternative strategy for the benzene-free synthesis of aromatic chemicals

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Biflavones from the genus Podocarpus

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12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/CPB.56.585

Identifiers

DOI

10.1248/CPB.56.585

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16 September 2017

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