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Volumn 19, Issue 8, 2001, Pages 2309-2318

Phase I clinical and pharmacokinetic study of rebeccamycin analog NSC 655649 given daily for five consecutive days

Author keywords

[No Author keywords available]

Indexed keywords

1,11 DICHLORO 6 (2 DIETHYLAMINOETHYL) 12,13 DIHYDRO 5H INDOLO[2,3 A]PYRROLO[3,4 C]CARBAZOLE 5,7(6H) DIONE 13 (4 O METHYLGLUCOSIDE); ANTINEOPLASTIC AGENT; CARBAZOLE DERIVATIVE; ONDANSETRON; PROCHLORPERAZINE; REBECCAMYCIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035871186     PISSN: 0732183X     EISSN: None     Source Type: Journal    
DOI: 10.1200/JCO.2001.19.8.2309     Document Type: Article
Times cited : (32)

References (16)
  • 4
    • 9844260513 scopus 로고    scopus 로고
    • Syntheses and biological activities (topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group
    • (1997) J Med Chem , vol.40 , pp. 3456-3465
    • Anizon, F.1    Belin, L.2    Moreau, P.3
  • 9
    • 0000714445 scopus 로고    scopus 로고
    • Structure-activity relationships in a series of substituted indolocarbazoles: Topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
    • (1996) J Med Chem , vol.39 , pp. 4471-4477
    • Pereira, E.R.1    Belin, L.2    Sancelme, M.3
  • 10
    • 0004992101 scopus 로고    scopus 로고
    • A phase I clinical and pharmacokinetic study of the rebeccamycin analog NSC 655649 in patients with advanced cancer
    • Abstract 250, Presented at the EORTC/NCI New Drug Development Meeting, Amsterdam, the Netherlands, June 16-19, 1998
    • (1998) Ann Oncol , vol.9 , Issue.SUPPL. 2 , pp. 66
    • Eckhardt, S.G.1    Kuhn, J.2    Rizzo, S.3
  • 16
    • 85037405309 scopus 로고    scopus 로고
    • Cytochrome P-450 metabolism of the rebeccamycin analog NSC 655649
    • Presented at the EORTC/NCI New Drug Development Meeting. Amsterdam, the Netherlands, June 16-19, 1998. (abstr 231)
    • (1998) Ann Oncol , vol.9 , pp. 61
    • Rizzo, J.1    Renouf, J.2    Eckhardt, S.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.