(Q43674996)

25 November 2017

Antimalarial halorosellinic acid from the marine fungus Halorosellinia oceanica (English)

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25 November 2017

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Halorosellinia oceanica

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(1R,3R,4R,7S,11S)-12-[(E,2R,3R,4S)-6-carboxy-3,4-dihydroxyhept-5-en-2-yl]-1,4-dimethyltricyclo[9.3.0.03,7]tetradeca-8,12-diene-8-carboxylic acid

1 reference

(1S,3S,4S,7R,8E,11R)-12-[(E,2S,3S,4R)-6-carboxy-3,4-dihydroxyhept-5-en-2-yl]-1,4-dimethyltricyclo[9.3.0.03,7]tetradeca-8,12-diene-8-carboxylic acid

1 reference

(2E,3R)-2-hexylidene-3-methylbutanedioic acid

1 reference

1 reference

(1R,3R,4R,7S,11S)-12-[(1R)-1-[(4R)-5-[(E)-2-carboxyprop-1-enyl]-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl]-1,4-dimethyltricyclo[9.3.0.03,7]tetradeca-8,12-diene-8-carboxylic acid

1 reference

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

1 reference

(1R,3R,4R,7S,8E,11S)-12-[(1R)-1-[(4R)-5-[(E)-2-carboxyprop-1-enyl]-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl]-1,4-dimethyltricyclo[9.3.0.03,7]tetradeca-8,12-diene-8-carboxylic acid

1 reference

(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid

1 reference

(E)-2-[(2R)-1-methoxy-1-oxopropan-2-yl]oct-2-enoic acid

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2

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25 November 2017

Chinworrungsee M

1

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25 November 2017

Isaka M

3

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25 November 2017

Rungrod A

4

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25 November 2017

Tanticharoen M

5

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25 November 2017

Thebtaranonth Y

6

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Bioorganic & Medicinal Chemistry Letters

25 November 2017

language of work or name

English

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publication date

August 2001

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16 September 2022

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25 November 2017

11

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25 November 2017

15

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25 November 2017

1965-1969

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Bioactive naphthoquinones from Cordyceps unilateralis

25 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Antimalarial activity of macrocyclic trichothecenes isolated from the fungus Myrothecium verrucaria

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Cordyanhydrides A and B. Two unique anhydrides from the insect pathogenic fungus Cordyceps pseudomilitaris BCC 1620

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Antiplasmodial compounds from the wood-decayed fungus Xylaria sp. BCC 1067.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Coumarins and carbazoles with antiplasmodial activity from Clausena harmandiana

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

An antimalarial stilbene from Artocarpus integer

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Antimalarial preracemosols A and B, possible biogenetic precursors of racemosol from Bauhinia malabarica Roxb

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Phyllanthusols A and B, cytotoxic norbisabolane glycosides from Phyllanthus acidus Skeels

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Metabolites of the higher fungi. Part 22. 2-Butyl-3-methylsuccinic acid and 2-hexylidene-3-methylsuccinic acid from xylariaceous fungi

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Metabolites of the higher fungi. Part 24. Cytochalasin N, O, P, Q, and R. New cytochalasins from the fungus Hypoxylon terricola Mill

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

New cytochalasins from the fungus Xylaria hypoxylon

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Human malaria parasites in continuous culture

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

New colorimetric cytotoxicity assay for anticancer-drug screening

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Structure and conformation of ophiobolin K and 6- epiophiobolin K from Aspergillus ustus as a nematocidal agent.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

The Structure of Ophiobolin, a C25 Terpenoid Having a Novel Skeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Some new phytotoxic ophiobolins produced by Drechslera oryzae

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Microbial metabolites of ophiobolin A and antimicrobial evaluation of ophiobolins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Ophiobolin M and analogues, noncompetitive inhibitors of ivermectin binding with nematocidal activity.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

Characterization of 6-epi-3-anhydroophiobolin B from Cochliobolus heterostrophus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900327-4

7 January 2021

10.1016/S0960-894X(01)00327-4

Identifiers

DOI

1 reference

25 November 2017

1 reference