DU145型
体内
药理学
前列腺癌
化学
前列腺
癌症
LNCaP公司
生物
医学
内科学
生物技术
作者
Masahiro Ueda,Tadashi Shimizu,Miyuki Mabuchi,Kota Horiike,Kaori Kitae,Hiroaki Hase,Yuko Ueda,Kazutake Tsujikawa,Akito Tanaka
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2018-01-02
卷期号:38 (1)
被引量:3
标识
DOI:10.21873/anticanres.12210
摘要
Novel potent prostate cancer antigen-1 (PCA-1)/alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 (ALKBH3) inhibitors both in vivo and in vivo were designed and evaluated by a stability assay in an S9 mixture, a mixture of rat liver homogenate and co-factors, and oral absorbability assay in rat, as well as enzyme and cell assays, and resulted in the synthesis of a novel potent PCA-1/ALKBH3 inhibitor in vivo. Among them, compound 7l exhibited potent inhibitory activities in a xenograft model bearing DU145 tumor at 10 mg/kg by subcutaneous administration without negative side-effects. This inhibitory activity in vivo was more potent than that of HUHS015 at 32 mg/kg, a known PCA-1/ALKBH3 inhibitor, or docetaxel at 2.5 mg/kg, the drug clinically used for androgen-independent prostate cancer.
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