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Volumn 12, Issue 5, 2001, Pages 401-417

Quinone isomers of the WS-5995 antibiotics: Synthetic antitumor agents that inhibit macromolecule synthesis, block nucleoside transport, induce DNA fragmentation, and decrease the growth and viability of L1210 leukemic cells more effectively than ellagic acid and genistein in vitro

Author keywords

Apoptosis; DNA cleavage; Ellagic acid; Genistein; L1210 cells; Macromolecule synthesis; Mitotic index; Nucleoside transport; Tumor cell growth and viability; WS 5995 antibiotics

Indexed keywords

1,10 DIMETHOXY 8 METHYL 11,12 DIHYDRO 6H DIBENZO[C,H]CHROMENE 6,11,12 TRIONE; 7,12 DIHYDRO 5H DIBENZO[C,G]CHROMENE 5,7,12 TRIONE; ANTINEOPLASTIC ANTIBIOTIC; CASPASE; CYCLOHEXIMIDE; DACTINOMYCIN; DNA FRAGMENT; ELLAGIC ACID; ENDONUCLEASE; GENISTEIN; KETONE; PURINE NUCLEOSIDE; PYRIMIDINE NUCLEOSIDE; QUINONE DERIVATIVE; TOSYLPHENYLALANYL CHLOROMETHYL KETONE; UNCLASSIFIED DRUG; WS 5995; WS 5995A; ZINC SULFATE;

EID: 0034932934     PISSN: 09594973     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001813-200106000-00002     Document Type: Article
Times cited : (17)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.