(Q44565411)

4 December 2017

title

Diterpenoids from Neoboutonia glabrescens (Euphorbiaceae). (English)

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(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

4 December 2017

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[(1R,2S,5S,6R,7R,11R,12R,13S,14S)-2,13,14-triacetyloxy-6-hydroxy-3,7-dimethyl-9-oxo-15-oxatetracyclo[10.2.1.01,5.06,11]pentadec-3-en-13-yl]methyl acetate

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17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

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[(1R,2S,4R,5S,6S,10S,11S,12R,14S,16R)-5,6,11-trihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethyl-7-oxo-3-oxapentacyclo[9.5.0.02,4.06,10.014,16]hexadec-8-en-14-yl] dodecanoate

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acetyl aleuritolic acid

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9-methoxy-1,7-dimethylphenanthrene

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(1R,2S,5S,6R,7R,11R,12R,13R,14R)-2,6,13,14-tetrahydroxy-13-(hydroxymethyl)-3,7-dimethyl-15-oxatetracyclo[10.2.1.01,5.06,11]pentadec-3-en-9-one

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(1R,2R,6S,7S,8R,10S,11S,12R,14R,16R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-16-prop-1-en-2-yl-14-undecyl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one

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(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one

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(1R,2R,6S,7S,8R,10S,11S,12R,14S,16R,18R)-6,7-Dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-16-prop-1-en-2-yl-14-undecyl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-5-one

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[(1R,2R,3R,4R,5S,8S,9S,10R,13R,16S)-3,5-diacetyloxy-2,9-dihydroxy-6,10,14,14-tetramethyl-12-oxo-15,17-dioxapentacyclo[7.6.1.11,4.04,8.013,16]heptadec-6-en-2-yl]methyl acetate

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(2R)-2,8-dihydroxy-5-methoxy-3,3,7-trimethyl-2H-cyclopenta[a]naphthalen-1-one

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(2R)-6-(1,3-benzodioxol-5-yl)-4,5-dimethoxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one

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(1S,2S,5S,6R,7S,8S,9R,12R,15R,16R)-1,5,6,7,8-pentahydroxy-8-(hydroxymethyl)-4,11,11,15-tetramethyl-10-oxatetracyclo[7.6.1.02,6.012,16]hexadec-3-en-13-one

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[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16R,18R)-6,7-dihydroxy-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-14-undecyl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-8-yl]methyl hexadecanoate

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3,4,3'-Tri-O-methylellagic acid

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(1R,2S,5S,6R,7R,11R,12R,13S,14R)-2,6,13,14-tetrahydroxy-13-(hydroxymethyl)-3,7-dimethyl-15-oxatetracyclo[10.2.1.01,5.06,11]pentadec-3-en-9-one

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[(1R,2R,6S,7S,8R,10S,11S,12R,14S,16R,18S)-6,7-dihydroxy-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-14-undecyl-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-8-yl]methyl hexadecanoate

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Euphorbia cheiradenia

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Euphorbia lamprocarpa

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Euphorbia ampliphylla

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Euphorbia polygonifolia

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Euphorbia sessiliflora

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Euphorbia balsamifera

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Euphorbia cattimandoo

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Euphorbia helioscopia

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4 December 2017

Pierre Tane

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4 December 2017

Mathieu Tene

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4 December 2017

Alembert T Tchinda

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4 December 2017

Pierre Kamnaing

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4 December 2017

David Ngnokam

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4 December 2017

Johnson F Ayafor

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4 December 2017

Joseph D Connolly

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4 December 2017

Louis J Farrugia

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4 December 2017

language of work or name

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September 2003

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16 September 2022

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inferred from page(s)

published in

Phytochemistry

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4 December 2017

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4 December 2017

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4 December 2017

page(s)

575-581

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On the active principles of the spurge family, X. Skin irritants, cocarcinogens, and cryptic cocarcinogens from the latex of the manchineel tree

4 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Novel bioactive diterpenoids from Aframomum aulacocarpos

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

WinGXsuite for small-molecule single-crystal crystallography

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https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Rhamnofolane derivatives from Jatropha grossidentata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Daphnane Diterpenes from Wikstroemia monticola: Wikstrotoxins A-D, Huratoxin, and Excoecariatoxin

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Structure of Trigonostemone, a New Phenanthrenone from the Thai Plant Trigonostemon reidioides

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https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Isolation and structural elucidation of new potent antileukemic diterpenoid esters from Gnidia species

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Novel bioactive phenanthrene derivatives from Domohinea perrieri

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Unambiguous structural and nuclear magnetic resonance spectral characterization of two triterpenoids of Maprouneaguianensis by two-dimensional nuclear magnetic resonance spectroscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

NMR spectral analysis of polyphenols from Punica granatum

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7 January 2021

Potential anticancer agents VIII. Constituents of Baliospermum montanum (Euphorbiaceae)

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7 January 2021

Processing of X-ray diffraction data collected in oscillation mode

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

A phorbol derivative from croton rhamnifolius

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Anti-plasmodial sesquiterpenoids from the African Reneilmia cincinnata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

3-Acetylaleuritolic acid from the seeds of Phytolacca americana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Polyphenols of Eucalyptus globulus, E. Regnans and E. Deglupta

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

Diterpenes and sterols from Neoboutonia melleri

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2803%2900158-4

7 January 2021

10.1016/S0031-9422(03)00158-4

Identifiers

DOI

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4 December 2017

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