Six new 10-pheynl-[11]cytochalasans, cytochalasins N - S from phomopsis SP. (Q104394287)

(1R,2R,3Z,5R,7S,9Z,11R,12S,14R,15S,16R,17S)-17-benzyl-2,5-dihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.01,16.012,14]nonadeca-3,9-dien-19-one

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[(1R,2R,3Z,5R,7S,9Z,11R,12S,13S,14S,15R,16S)-16-benzyl-5,12,13-trihydroxy-5,7,13,14-tetramethyl-18-oxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9-dien-2-yl] acetate

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(1S,2R,5R,7S,9E,11R,12S,14S,15R,16S)-16-benzyl-2,5,12-trihydroxy-5,7,14-trimethyl-13-methylidene-17-azatricyclo[9.7.0.01,15]octadeca-3,9-dien-18-one

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[(1R,2R,3E,5R,7R,9E,11S,12S,14R,15R,16R,17R)-17-benzyl-5-hydroxy-5,7,14,15-tetramethyl-6,19-dioxo-13-oxa-18-azatetracyclo[9.8.0.01,16.012,14]nonadeca-3,9-dien-2-yl] acetate

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(1R,2R,3Z,5R,7S,9Z,11R,12S,15R,16S)-16-benzyl-2,5,12-trihydroxy-5,7,13,14-tetramethyl-17-azatricyclo[9.7.0.01,15]octadeca-3,9,13-trien-18-one

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[(1R,2R,3E,5R,7R,9R,11R,12S,13S,15R,16R,17R,18R)-18-benzyl-5-hydroxy-5,7,15,16-tetramethyl-6,20-dioxo-10,14-dioxa-19-azapentacyclo[10.8.0.01,17.09,11.013,15]icos-3-en-2-yl] acetate

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[(1R,2R,3Z,5R,7S,9Z,11R,12S,14R,15S,16R,17S)-17-benzyl-5-hydroxy-5,7,14,15-tetramethyl-19-oxo-13-oxa-18-azatetracyclo[9.8.0.01,16.012,14]nonadeca-3,9-dien-2-yl] acetate

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[(1R,2R,3Z,5R,7S,9Z,11R,12S,15R,16S)-16-benzyl-5,12-dihydroxy-5,7,13,14-tetramethyl-18-oxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,13-trien-2-yl] acetate

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(1S,2R,3Z,5R,7S,9Z,11R,12S,13S,14S,15R,16S)-16-benzyl-2,5,12,14-tetrahydroxy-5,7,13,14-tetramethyl-17-azatricyclo[9.7.0.01,15]octadeca-3,9-dien-18-one

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(13E,19E)-10-Phenyl-16alpha,18beta-dimethyl-18-hydroxy-21beta-acetoxy-6,7beta-epoxy[11]cytochalasa-13,19-diene-1,17-dione

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[(1R,2R,3E,5R,7S,9E,11R,12S,15S,16S)-16-benzyl-5,12-dihydroxy-5,7,13,14-tetramethyl-18-oxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,13-trien-2-yl] acetate

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Yoshihiko Izawa

1

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

Takashi Hirose

2

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

Takako Shimizu (née Tomioka)

3

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

Kiyotaka Koyama

4

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

Shinsaku Natori

5

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

publication date

January 1989

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

volume

45

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2983434-7

page(s)

2323-2335

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issue

8

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cites work

Chemical Surveys on Mycotoxins Using Cytotoxicity Testing with Special Reference to Cytochalasans

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https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Toxicity and plant growth regulator effects of cytochalasin H isolated from Phomopsis sp

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Metabolites of Cercospora. Taiwapyrone, an α-pyrone of unusual structure from Cercospora taiwanensis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Screening of the genus Cercospora for secondary metabolites☆

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https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Structure of a new [11]cytochalasin, cytochalasin H or kodo-cytochalasin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Proton and carbon-13 nuclear magnetic resonance studies of the conformation of cytochalasin H derivatives and plant growth regulating effects of cytochalasins

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021

Structure-activity relationship of thirty-nine cytochalasans observed in the effects on cellular structures and cellular events and on actin polymerization in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2983434-7

7 January 2021