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公司基本資料信息
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PNU-159682 is a major bioactive metabolite of Nemorubicin in human liver microsomes; > 3,000-fold cytotoxic than its parent compound(MMDX and doxorubicin).
IC50 value: 0.1-0.5 nM (HT-29; DU145; Jurkat cell lines, etc) [1]
Target: Topoisomerase I inhibitor
in vitro: The cytotoxicity of PNU-159682 were in the subnanomolar range (0.07-0.58 nmol/L) and noticeably lower than that recorded for both MMDX and doxorubicin; PNU-159682 was 2,360- to 790-fold and 6,420- to 2,100-fold more potent than MMDX and doxorubicin, respectively [1].
in vivo: An evaluation of the in vivo antitumor activity of PNU-
159682, in comparison with that of MMDX, was then conducted
in mice bearing disseminated murine L1210 leukemia.
MCE 對每批產(chǎn)品都進(jìn)行嚴(yán)格的LCMS和NMR檢驗,其產(chǎn)品已被全球近萬名客戶廣泛使用并發(fā)表大量文章、專利;
MCE 定期增加各領(lǐng)域熱門抑制劑、激動劑,不斷擴(kuò)增已有化合物庫,以滿足最新的科研需求;
數(shù)千種產(chǎn)品在上海有充足備貨,24-48小時內(nèi)送達(dá)客戶;
大量產(chǎn)品提供免費試用裝;
已為全球多個知名企業(yè)、院校構(gòu)建各種定制型化合物庫。
產(chǎn)品鏈接:
http://www.medchemexpress.cn/pnu-159682.html