Using spectroscopic and database strategies to unravel structures of polycyclic bioactive marine sponge sesterterpenes (Q105113575)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2980872-3

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4-[(1E)-2-(1,2,4a,8,8-pentamethyl-3,4,4b,5,6,7,10,10a-octahydro-2H-phenanthren-1-yl)ethenyl]-5-hydroxy-5H-furan-2-one

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Phillip Crews

1

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2980872-3

Carlos Jiménez

series ordinal

2

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2980872-3

Mark O'Neil-Johnson

series ordinal

3

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2980872-3

publication date

January 1991

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2801%2980872-3

volume

47

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issue

22

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page(s)

3585-3600

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Inactivation of bee venom phospholipase A2 by manoalide. A model based on the reactivity of manoalide with amino acids and peptide sequences

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Sesterterpenes from a common marine sponge, Hyrtios erecta

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The luffariellins, novel antiinflammatory sesterterpenes of chemotaxonomic importance from the marine sponge Luffariella variabilis

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Manoalide, an antibiotic sesterterpenoid from the marine sponge (polejaeff)

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Chemistry of Sponges, III. Manoalide Monoacetate and Thorectolide Monoacetate, Two New Sesterter-penoids from Thorectandra excavatus

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Verrucosin-a and -b, ichthyotoxic diterpenoic acid glycerides with a new carbon skeleton from the dorid nudibranch doris verrucosa

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Diterpenes from the sponge Dysidea amblia

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Two new metabolites of the sponge Dysidea amblia and revision of the structure of ambliol B

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Structure analysis of rimuene by 13C nmr spectroscopy

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Luffolide, a novel anti-inflammatory terpene from the sponge Luffariella sp..

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The structure and conformational properties of a cembranolide diterpene from Pachyclavularia violacea

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Novel marine sponge alkaloids. 1. Plakinidine A and B, anthelmintic active alkaloids from a Plakortis sponge

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Enantiomeric Relationships and Anthelmintic Activity of Dysinin Derivatives from Dysidea Marine Sponges

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