Structure determination, conformational analysis, chemical stability studies, and antitumor evaluation of the cryptophycins. Isolation of 18 new analogs from Nostoc sp. strain GSV 224 (Q78319577)

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scientific article published on 19 March 2005

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English	Structure determination, conformational analysis, chemical stability studies, and antitumor evaluation of the cryptophycins. Isolation of 18 new analogs from Nostoc sp. strain GSV 224	scientific article published on 19 March 2005

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scholarly article

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Structure determination, conformational analysis, chemical stability studies, and antitumor evaluation of the cryptophycins. Isolation of 18 new analogs from Nostoc sp. strain GSV 224 (English)

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

1 reference

Cryptophycin 23

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Cryptophycin-19

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(2S)-3-[[(2R)-3-(3-chloro-4-methoxyphenyl)-2-[[(E,5S,6R)-5-[(2S)-2-hydroxy-4-methylpentanoyl]oxy-6-[(2S,3R)-3-phenyloxiran-2-yl]hept-2-enoyl]amino]propanoyl]amino]-2-methylpropanoic acid

1 reference

Cryptophycin 49

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(13E)-10-[(3-chloro-4-methoxyphenyl)methyl]-16-(3,4-dihydroxy-4-phenylbutan-2-yl)-6-methyl-3-(2-methylpropyl)-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone

1 reference

(2E)-N-[2-(3-chloro-4-methoxyphenyl)-1-{[2-methyl-2-(methyl-C-hydroxycarbonimidoyl)ethyl]-C-hydroxycarbonimidoyl}ethyl]-5-hydroxy-6-(3-phenyloxiran-2-yl)hept-2-enimidic acid

1 reference

(3S,6R,10S,13Z,16S)-10-[(3-chloro-4-methoxyphenyl)methyl]-6-methyl-3-(2-methylpropyl)-16-[(1R)-1-[(2R,3R)-3-phenyloxiran-2-yl]ethyl]-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone

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Cryptophycin 50

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Cryptophycin 24

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(13E)-10-[(3-chloro-4-methoxyphenyl)methyl]-16-(3-hydroxy-4-methoxy-4-phenylbutan-2-yl)-6-methyl-3-(2-methylpropyl)-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone

1 reference

Cryptophycin-40

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Cryptophycin-28

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Cryptophycin-43

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1 reference

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Cryptophycin-31

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Cryptophycin 16

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(3R,6R,10R,13E,16S)-16-[(2S,3R)-3-chloro-2-hydroxy-3-phenylpropyl]-10-[(3-chloro-4-methoxyphenyl)methyl]-6-methyl-3-(2-methylpropyl)-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone

1 reference

Cryptophycin-45

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(2S)-3-[[(2R)-3-(3-chloro-4-methoxyphenyl)-2-[[(E)-4-(4-hydroxy-3-methyl-5-phenyloxolan-2-yl)but-2-enoyl]amino]propanoyl]amino]-2-methylpropanoic acid

1 reference

1 reference

(2R)-3-(3-chloro-4-methoxyphenyl)-2-[[(E)-4-[(3R,4R)-4-hydroxy-3-methyl-5-phenyloxolan-2-yl]but-2-enoyl]amino]propanoic acid

1 reference

Cryptophycin-29

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Cryptophycin 30

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Cryptophycin-21

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(2E)-N-[2-(3-chloro-4-methoxyphenyl)-1-{[2-methyl-2-(methyl-C-hydroxycarbonimidoyl)ethyl]-C-hydroxycarbonimidoyl}ethyl]-5-[(2-hydroxy-4-methylpentanoyl)oxy]-6-(3-phenyloxiran-2-yl)hept-2-enimidic acid

1 reference

Cryptophycin-17

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(13E)-16-(4-bromo-3-hydroxy-4-phenylbutan-2-yl)-10-[(3-chloro-4-methoxyphenyl)methyl]-6-methyl-3-(2-methylpropyl)-1,4-dioxa-8,11-diazacyclohexadec-13-ene-2,5,9,12-tetrone

1 reference

Cryptophycin-54

1 reference

1 reference

(2S)-3-[[(2R)-3-(3-chloro-4-methoxyphenyl)-2-[[(2E,5S,6S,7E)-5-hydroxy-6-methyl-8-phenylocta-2,7-dienoyl]amino]propanoyl]amino]-2-methylpropanoic acid

1 reference

Cryptophycin-18

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Cryptophycin-16

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1 reference

Cryptophycin-26

1 reference

Cryptophycin-24

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(2R)-3-[[(2R)-3-(3-chloro-4-methoxyphenyl)-2-[[(E,5S,6S,7R,8S)-5,7-dihydroxy-8-methoxy-6-methyl-8-phenyloct-2-enoyl]amino]propanoyl]amino]-2-methylpropanoic acid

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1 reference

Cryptophycin 18

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1 reference

Cryptophycin 29

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1 reference

[(E,2S,3S)-7-[[(2R)-3-(3-chloro-4-methoxyphenyl)-1-[[(2R)-3-methoxy-2-methyl-3-oxopropyl]amino]-1-oxopropan-2-yl]amino]-7-oxo-2-[(2R,3R)-3-phenyloxiran-2-yl]hept-5-en-3-yl] (2S)-2-hydroxy-4-methylpentanoate

1 reference

author name string

Trimurtulu Golakoti

1

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Junichi Ogino

2

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Carl E. Heltzel

3

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Trang Le Husebo

4

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Craig M. Jensen

5

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Linda K. Larsen

6

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Gregory M. L. Patterson

7

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Richard E. Moore

8

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Susan L. Mooberry

9

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Thomas H. Corbett

10

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Frederick A. Valeriote

11

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

language of work or name

1 reference

Journal of the American Chemical Society

publication date

1 December 1995

1 reference

16 September 2022

Journal of the American Chemical Society

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10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

117

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10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

49

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10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

12030-12049

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

Identifiers

10.1021/JA00154A002

1 reference

10.1021/JA00154A002

https://api.crossref.org/v1/works/http://dx.doi.org/10.1021/ja00154a002

13 December 2019

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