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Volumn 19, Issue 8, 2002, Pages 1215-1222

Stable supersaturated aqueous solutions of silatecan 7-t-butyldimethylsilyl-10-hydroxycamptothecin via chemical conversion in the presence of a chemically modified β-cyclodextrin

Author keywords

Camptothecin analogs; Cyclodextrin complexes; Lactone hydrolysis; Parenteral formulation; Solubilization

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; ANTINEOPLASTIC AGENT; BETA CYCLODEXTRIN; BETA CYCLODEXTRIN SULFOBUTYL ETHER; CAMPTOTHECIN DERIVATIVE; CARBOXYLIC ACID; DB 67; DIMETHYL SULFOXIDE; FUNCTIONAL GROUP; LACTONE; SILATECAN 7 TERT BUTYLDIMETHYLSILYL 10 HYDROXYCAMPTOTHECIN; SOLVENT; UNCLASSIFIED DRUG; WATER;

EID: 0036689443     PISSN: 07248741     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1019862629357     Document Type: Article
Times cited : (37)

References (17)
  • 6
    • 0024420685 scopus 로고
    • Arrest of replication forks by drug-stabilized topoisopomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin
    • (1989) Cancer Res. , vol.49 , pp. 5077-5082
    • Hsiang, Y.H.1    Lihou, M.G.2    Liu, L.F.3
  • 10
    • 0031796343 scopus 로고    scopus 로고
    • Irinotecan in lymphoma, leukemia, and breast, pancreatic, ovarian, and small-cell lung cancers
    • (1998) Oncology (Huntingt) , vol.12 , pp. 103-109
    • Rosen, L.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.