(Q104947368)

English

Anti-tumor agents. 136. Cumingianosides A-F, potent antileukemic new triterpene glucosides, and cumindysosides A and B, trisnor- and tetranortriterpene glucosides with a 14,18-cycloapoeuphane-type skeleton from Dysoxylum cumingianum

scientific article published on 12 March 2005

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scholarly article

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Anti-tumor agents. 136. Cumingianosides A-F, potent antileukemic new triterpene glucosides, and cumindysosides A and B, trisnor- and tetranortriterpene glucosides with a 14,18-cycloapoeuphane-type skeleton from Dysoxylum cumingianum (English)

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http://api.crossref.org/works/10.1021%2Fjo00051a050

Dysoxylum cumingianum

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cumingianoside A

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[(2R,3S,4S,5R,6R)-6-[[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-7-acetyloxy-15-[(2R,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-2,6,6,10-tetramethyl-3-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

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cumingianoside B

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Cumindysoside B

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[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-2,6,6,10-tetramethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-15-[(2R,4S,5S)-4,5,6-trihydroxy-6-methylheptan-2-yl]-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] acetate

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cumingianoside D

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[(2R,3S,4S,5R,6R)-6-{[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-7-(acetyloxy)-15-[(2R,4S,5S)-4,5-dihydroxy-6-methylhept-6-en-2-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]octadecan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl acetate

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cumingianoside F

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Cumindysoside A

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cumingianoside E

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[(2R,3S,4S,5R,6R)-6-[[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-7-acetyloxy-15-[(2R,4R,5R)-4,5-dihydroxy-6-methoxy-6-methylheptan-2-yl]-2,6,6,10-tetramethyl-3-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

1 reference

[(2R,3S,4S,5R,6R)-6-[[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(2R,4S)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7-hydroxy-2,6,6,10-tetramethyl-3-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

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cumingianoside C

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Epicharis cumingiana

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6

object named as

Kuo Hsiung Lee

1 reference

http://api.crossref.org/works/10.1021%2Fjo00051a050

author name string

Yoshiki Kashiwada

1

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http://api.crossref.org/works/10.1021%2Fjo00051a050

Toshihiro Fujioka

2

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http://api.crossref.org/works/10.1021%2Fjo00051a050

Jer Jang Chang

3

1 reference

http://api.crossref.org/works/10.1021%2Fjo00051a050

Ih Sheng Chen

4

1 reference

http://api.crossref.org/works/10.1021%2Fjo00051a050

Kunihide Mihashi

5

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http://api.crossref.org/works/10.1021%2Fjo00051a050

publication date

December 1992

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16 September 2022

Journal of Organic Chemistry

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http://api.crossref.org/works/10.1021%2Fjo00051a050

57

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http://api.crossref.org/works/10.1021%2Fjo00051a050

25

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http://api.crossref.org/works/10.1021%2Fjo00051a050

6946-6953

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http://api.crossref.org/works/10.1021%2Fjo00051a050

Identifiers

10.1021/JO00051A050

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