The absolute stereochemistry and cytotoxicity of the ascidian-derived metabolite, longithorone J

Natural Product Research

Volumn 20, Issue 14, 2006, Pages 1277-1282

  Davis, Rohan A ^a   Carroll, Anthony R ^a   Watters, Dianne ^a   Quinn, Ronald J ^a  

^a GRIFFITH UNIVERSITY   (Australia)

Author keywords

Absolute stereochemistry; Aplidium longithorax; Ascidian; Cytotoxicity; Longithorone J; Longithorone K; Mosher method; Natural product

Indexed keywords

ANTINEOPLASTIC AGENT; LISSOCLINOTOXIN E; LISSOCLINOTOXIN F; LONGITHORONE J; LONGITHORONE K; NATURAL PRODUCT; UNCLASSIFIED DRUG; BRIDGED COMPOUND; LONGITHORONE A; POLYCYCLIC HYDROCARBON; QUINONE DERIVATIVE;

ANTINEOPLASTIC ACTIVITY; APLIDIUM LONGITHORAX; ARTICLE; ASCIDIACEA; BIOSYNTHESIS; CANCER CELL CULTURE; CELL PROLIFERATION; CELL STRAIN HEK293; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOTOXICITY; DRUG STRUCTURE; HUMAN; HUMAN CELL; IC 50; MOLECULAR MODEL; NONHUMAN; STEREOCHEMISTRY; ANIMAL; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECT; NUCLEAR MAGNETIC RESONANCE; STEREOISOMERISM; TUMOR CELL LINE; UROCHORDATA;

APLIDIUM; ASCIDIA; LONGITHORAX;

ANIMALS; BRIDGED COMPOUNDS; CELL LINE, TUMOR; CELL PROLIFERATION; HUMANS; MODELS, MOLECULAR; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; POLYCYCLIC COMPOUNDS; QUINONES; STEREOISOMERISM; UROCHORDATA;

EID: 34247599308     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786410601101811     Document Type: Article

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