Composition sterolique et morphogeneses reproductrices chez Gnomonia leptostyla (Q104917658)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981882-8

1 reference

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

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(3S,9R,10R,13R,14S,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

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(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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

1 reference

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

1 reference

(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2S,5R)-5,6-dimethylhept-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-ol

1 reference

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

1 reference

(3S,5R,9R,10S,13R,14R,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

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

1 reference

(3S,4R,8S,9S,10R,13R,14R,17R)-17-[(E,2S,5R)-5,6-dimethylhept-3-en-2-yl]-4,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

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

1 reference

(3S,9R,10R,13R,14S,17R)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

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J. Fayret

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981882-8

L. Lacoste

2

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J. Alais

3

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A. Lablache-Combier

4

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A. Maquestiau

5

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981882-8

Y. Van Harverbeke

6

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R. Flammang

7

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2800%2981882-8

H. Mispreuve

8

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publication date

January 1979

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16 September 2022

5

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inferred from page(s)

published in

Phytochemistry

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volume

18

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issue

3

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page(s)

431-435

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Sterols of the Fungi: Distribution and Biosynthesis

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Study of complex marine sterol mixtures by mass-analyzed ion kinetic energy spectrometry

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7 January 2021

Identification by Combined Gas–Liquid Chromatography – Mass Spectrometry of Sterols Isolated from Scenedesmus obliquus Grown in Light and Heavy Water

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7 January 2021

The identification of 24-methylene-24,25-dihydrolanosterol and other possible ergosterol precursors in Phycomyces blakesleeanus and Agaricus campestris

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7 January 2021

Sterol Biosynthesis in Euglena gracilis Z. Comparative Study of Free and Bound Sterols in Light and Dark Grown Euglena gracilis Z

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7 January 2021

Metabolism of delta7- and delta5,7-sterols by Phytophthora cactorum

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7 January 2021

Design and Performance of a Mass-analyzed Ion Kinetic Energy (MIKE) Spectrometer

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7 January 2021