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Volumn 66, Issue 7, 2001, Pages 2207-2216
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Synthesis, chemical properties, and biological evaluation of CC-1065 and duocarmycin analogues incorporating the 5-methoxycarbonyl-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one alkylation subunit
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Author keywords
[No Author keywords available]
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Indexed keywords
BIOLOGICAL EVALUATION;
ALKYLATION;
DNA;
SUPRAMOLECULAR CHEMISTRY;
X RAY ANALYSIS;
AROMATIC COMPOUNDS;
3 (5,6,7 TRIMETHOXYINDOL 2 CARBONYL) 1 (CHLOROMETHYL) 5 HYDROXY 6 METHOXYCARBONYL 1,2 DIHYDRO 3H BENZ[E]INDOLE;
DUOCARMYCIN DERIVATIVE;
N (5,6,7 TRIMETHOXYINDOL 2 CARBONYL) 5 METHOXYCARBONYL 1,2,9,9A TETRAHYDROCYCLOPROPA[C]BENZ[E]INDOL 4 ONE;
N (TERT BUTYLOXYCARBONYL) 5 METHOXYCARBONYL 1,2,9,9A TETRAHYDROCYCLOPROPA[C]BENZ[E]INDOL 4 ONE;
RACHELMYCIN;
RACHELMYCIN DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL ANALYSIS;
CHEMICAL BINDING;
CORRELATION FUNCTION;
DNA ALKYLATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
STEREOCHEMISTRY;
STEREOSPECIFICITY;
X RAY ANALYSIS;
ALKYLATION;
ANIMALS;
ANTIBIOTICS, ANTINEOPLASTIC;
ANTINEOPLASTIC AGENTS, ALKYLATING;
CRYSTALLOGRAPHY, X-RAY;
DNA;
INDOLES;
INHIBITORY CONCENTRATION 50;
KINETICS;
LEUCOMYCINS;
LEUKEMIA L1210;
MICE;
PYRROLES;
PYRROLIDINONES;
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EID: 0035815152
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo001772g Document Type: Article |
Times cited : (51)
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References (52)
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