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Journal of the American Chemical Society

Volumn 124, Issue 25, 2002, Pages 7405-7410

Toward computing relative configurations: 16-epi-latrunculin B, a new stereoisomer of the actin polymerization inhibitor latrunculin B

(7) Hoye, Thomas R a Ayyad, Seif Eldin N b Eklov, Brian M a Hashish, Nadia E c Thomas Shier, W c El Sayed, Khalid A d Hamann, Mark T d

a University of Minnesota (United States)

b MANSOURA UNIVERSITY (Egypt)

c UNIVERSITY OF MINNESOTA (United States)

d UNIVERSITY OF MISSISSIPPI (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOTOXICITY;

NUCLEAR MAGNETIC RESONANCE; POLYMERIZATION; TUMORS;

ISOMERS;

ACTIN; LATRUNCULIN B; NATURAL PRODUCT;

ANALYTIC METHOD; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHEMICAL COMPOSITION; COMPLEX FORMATION; CONTROLLED STUDY; CYTOTOXICITY; DRUG STRUCTURE; MOUSE; NONHUMAN; POLYMERIZATION; REACTION ANALYSIS; SPONGE (PORIFERA); STEREOCHEMISTRY; STEREOISOMERISM; STRUCTURE ANALYSIS; TUMOR CELL LINE; VALIDATION PROCESS;

ACTINS; ANIMALS; ANTINEOPLASTIC AGENTS; ANTIVIRAL AGENTS; BICYCLO COMPOUNDS, HETEROCYCLIC; HERPESVIRUS 1, HUMAN; MICE; MOLECULAR CONFORMATION; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PORIFERA; STEREOISOMERISM; THIAZOLES; THIAZOLIDINES; TUMOR CELLS, CULTURED;

EID: 0037178135 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja025734l Document Type: Article

Times cited : (23)

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