RRC ID 80086
著者 Quan HJ, Koyanagi J, Komada F, Saito S.
タイトル Preparations of vitamin D analogs, spirostanols and furostanols from diosgenin and their cytotoxic activities.
ジャーナル Eur J Med Chem
Abstract Vitamin D analogs 12 and 13 having a spiro ring in the side chain, various spirostanols 18-21, 26, 27, 29 and 37, and furostanols 34-36 having SCN and SeCN groups at the 26 position were prepared from diosgenin 1 via (20S,22R,25R)-spirost-1alpha,2alpha-epoxy-4,6-dien-3-one 19 as a key intermediate. The cytotoxic activities of these derivatives as well as 1 on scarcely P-gp-expressed HCT 116 cells and P-gp-overexpressed Hep G2 cells were examined by MTT assay. Furostanols 34 (IC(50) value: 4.9+/-0.3 microM) and 36 (IC(50) value: 1.3+/-0.2 microM) exhibited marked cytotoxic effects on HCT 116 cells, and spirostanol 29 (IC(50) value: 2.4+/-0.8 microM) and furostanol 36 (IC(50) value: 2.8+/-0.4 microM) on Hep G2 cells. Furthermore, the effects of vitamin D analog 12, spirostanol 26 and furostanol 36 on apoptosis-signaling pathways were investigated. Compounds 12 and 26 overexpressed p53 and Bax mRNAs, while compound 36 overexpressed only Bax mRNA.
巻・号 40(7)
ページ 662-73
公開日 2005-7-1
DOI 10.1016/j.ejmech.2005.02.003
PII S0223-5234(05)00050-4
PMID 15935901
MeSH Antineoplastic Agents / chemical synthesis* Antineoplastic Agents / pharmacology Cell Line, Tumor Cell Survival / drug effects Diosgenin / chemistry Drug Screening Assays, Antitumor Humans Proto-Oncogene Proteins c-bcl-2 / genetics RNA, Messenger / analysis RNA, Messenger / drug effects Spirostans / chemical synthesis* Spirostans / pharmacology Sterols / chemical synthesis* Sterols / pharmacology Structure-Activity Relationship Tumor Suppressor Protein p53 / genetics Vitamin D / analogs & derivatives* Vitamin D / pharmacology bcl-2-Associated X Protein
IF 5.573
リソース情報
ヒト・動物細胞 Hep G2(RCB0549)