Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge-Derived Fungus Aspergillus ustus (Q78234749)

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/hlca.201000283

12 December 2019

title

Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge-Derived Fungus Aspergillus ustus (English)

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/hlca.201000283

12 December 2019

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(1S,3R,6R,7S,9E,13R,15R,16R)-3,15-dimethyl-6-[(2S,3Z)-6-methylhepta-3,5-dien-2-yl]-12-oxatetracyclo[8.5.1.03,7.013,16]hexadec-9-ene-13,15-diol

1 reference

(1R)-7beta-[(1S,2Z)-1,5-Dimethyl-2,4-hexadienyl]-1,9abeta-dimethyl-2abeta-methoxy-2,2a,4,6,6aalpha,7,8,9,9a,10,10abeta,10bbeta-dodecahydro-1H-3-oxacyclopenta[5,6]cycloocta[1,2,3-cd]pentalene-1alpha-ol

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N-[(3S,4S,5S)-1-acetyl-5-(1,3-benzodioxole-5-carbonyl)-4-phenylpyrrolidin-3-yl]acetamide

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(6a)-21,21-O-dihydroophiobolin G

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N-[(3S,4S,5R)-1-acetyl-5-(1,3-benzodioxole-5-carbonyl)-4-phenylpyrrolidin-3-yl]acetamide

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(1S,3R,6R,7S,13S,15R,16S)-13-methoxy-3,15-dimethyl-6-[(2S)-6-methylhepta-3,5-dien-2-yl]-12-oxatetracyclo[8.5.1.03,7.013,16]hexadec-9-en-15-ol

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(1R)-7beta-[(1S,2Z)-1,5-Dimethyl-2,4-hexadienyl]-1,9abeta-dimethyl-2aalpha-methoxy-2,2a,4,6,6aalpha,7,8,9,9a,10,10abeta,10balpha-dodecahydro-1H-3-oxacyclopenta[5,6]cycloocta[1,2,3-cd]pentalene-1alpha-ol

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(1R,3S,7R,11R,12R)-8-(hydroxymethyl)-4-methyl-12-[(2S)-6-methylhepta-3,5-dien-2-yl]tricyclo[9.3.0.03,7]tetradeca-4,8-dien-6-one

1 reference

(1S,3R,6R,7S,13R,15R,16R)-13-methoxy-3,15-dimethyl-6-[(2S)-6-methylhepta-3,5-dien-2-yl]-12-oxatetracyclo[8.5.1.03,7.013,16]hexadec-9-en-15-ol

1 reference

(1R,3S,7R,8E,11R,12R)-8-(hydroxymethyl)-4-methyl-12-[(2S,3Z)-6-methylhepta-3,5-dien-2-yl]tricyclo[9.3.0.03,7]tetradeca-4,8-dien-6-one

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10

Peter Proksch

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12 December 2019

8

Victor Wray

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7

Werner E. G. Müller

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12 December 2019

9

Wen-Han Lin

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12 December 2019

3

Rainer Ebel

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12 December 2019

RuAngelie Edrada-Ebel

series ordinal

2

object named as

RuAngelie Edrada-Ebel

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12 December 2019

6

Siegfried Draeger

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12 December 2019

5

Barbara Schulz

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12 December 2019

author name string

Hong-Bing Liu

series ordinal

1

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12 December 2019

Yao Wang

series ordinal

4

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12 December 2019

publication date

April 2011

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16 September 2022

Helvetica Chimica Acta

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12 December 2019

volume

94

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issue

4

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12 December 2019

page(s)

623-631

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Marine-derived fungi: a chemically and biologically diverse group of microorganisms

12 December 2019

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1 reference

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A (1-->3)-beta-D-glucan recognition protein from the sponge Suberites domuncula. Mediated activation of fibrinogen-like protein and epidermal growth factor gene expression

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https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Sponge-associated fungi and their bioactive compounds: the Suberites case

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7 January 2021

Novel drimane sesquiterpene esters from Aspergillus ustus var. pseudodeflectus with endothelin receptor binding activity

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Metabolites Produced by Alternaria brassicae, the Black Spot Pathogen of Canola. Part 2, Sesquiterpenoid Metabolites

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7 January 2021

Sesquiterpenoids and benzofuranoids from the marine-derived fungus Aspergillus ustus 094102.

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7 January 2021

Drimane sesquiterpenoids from the fungus Aspergillus ustus isolated from the marine sponge Suberites domuncula.

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Aurantiamine, a diketopiperazine from two varieties of Penicillium aurantiogriseum

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7 January 2021

Isolation and structure determination of Pachybasium cerebrosides which potentiate the antifungal activity of aculeacin

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Ophiobolins G and H: new fungal metabolites from a novel source, Aspergillus ustus

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Cytotoxic sesterterpenes, 6-epi-ophiobolin G and 6-epi-ophiobolin N, from marine derived fungus Emericella variecolor GF10

1 reference

https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

L-657,398, a novel antifungal agent: fermentation, isolation, structural elucidation and biological properties

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https://api.crossref.org/works/10.1002%2FHLCA.201000283

7 January 2021

Identifiers

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