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Structure and stereochemistry of a novel bioactive sphingolipid from a Calyx sp
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scholarly article
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title
Structure and stereochemistry of a novel bioactive sphingolipid from a Calyx sp
(English)
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main subject
sphingolipids
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inferred from title
author name string
Bing-Nan Zhou
series ordinal
1
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Michael P Mattern
series ordinal
2
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Randall K Johnson
series ordinal
3
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David G.I Kingston
series ordinal
4
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publication date
November 2001
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published in
Tetrahedron
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volume
57
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issue
47
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page(s)
9549-9554
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cites work
Bioactive and other sesquiterpenes from Chiloscyphus rivularis.
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Minor and trace sterols from marine invertebrates. 50. Stereostructure and synthesis of nicasterol, a novel cyclopropane-containing sponge sterol
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New and known diketopiperazines from the Caribbean sponge, Calyx cf. podatypa.
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The calyxolanes: new 1,3-diphenylbutanoid metabolites isolated from the Caribbean marine sponge Calyx podatypa
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Antimicrobial N-methylpyridinium salts related to the xestamines from the Caribbean sponge Calyx podatypa
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Identification and total synthesis of novel fatty acids from the Caribbean sponge Calyx podatypa
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Oceanapiside, an antifungal bis-alpha,omega-amino alcohol glycoside from the marine sponge Oceanapia phillipensis
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Enantiodivergent Biosynthesis of the Dimeric Sphingolipid Oceanapiside from the Marine SpongeOceanapia phillipensis. Determination of Remote Stereochemistry
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BRS1, a C30 bis-amino, bis-hydroxy polyunsaturated lipid from an Australian calcareous sponge that inhibits protein kinase C.
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Identifiers
DOI
10.1016/S0040-4020(01)00958-9
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