S86733 |
Cevipabulin (TTI-237) |
源葉(MedMol) | 98% |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.151 ml | 10.757 ml | 21.514 ml |
5 mM | 0.43 ml | 2.151 ml | 4.303 ml |
10 mM | 0.215 ml | 1.076 ml | 2.151 ml |
50 mM | 0.043 ml | 0.215 ml | 0.43 ml |
- 提示:詳情請下載說明書。
- 產(chǎn)品描述: Cevipabulin (TTI-237) is an oral, microtubule-active antitumor compound and inhibits the binding of [3H] vinblastine to tubulin, with an IC50 of 18-40 nM for cytotoxicity in human tumor cell line
- 靶點: IC50: 18-40 nM (microtubule in human tumor cells);MicrotubuleAssociated
- 體內(nèi)研究:
Cevipabulin (TTI-2370)( 5, 10, 15, and 20 mg/kg, every 4 days for 4 cycles, in mice) is active by i.v. and p.o. administration against human tumor xenografts, showing dose-dependent effects, with good antitumor activity at 20 and 15 mg/kg. Animal Model: Athymic nu/nu female mice implanted s.c. in the flank with 1×107 LoVo human colon adenocarcinoma cells Dosage: 5, 10, 15, and 20 mg/kg Administration: I.V. injection every 4 days for 4 cycles. Result: The compound showed dose-dependent effects, with good antitumor activity at 20 and 15 mg/kg.
- 參考文獻:
1. Beyer CF, et al. TTI-237: a novel microtubule-active compound with in vivo antitumor activity. Cancer Res. 2008 Apr 1;68(7):2292-300. 2. Beyer CF, et al. The microtubule-active antitumor compound TTI-237 has both paclitaxel-like and vincristine-like properties. Cancer Chemother Pharmacol. 2009 Sep;64(4):681-9.
- 溶解性: Soluble in DMSO
- 保存條件: 2-8℃,避光
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 2.151 ml 10.757 ml 21.514 ml 5 mM 0.43 ml 2.151 ml 4.303 ml 10 mM 0.215 ml 1.076 ml 2.151 ml 50 mM 0.043 ml 0.215 ml 0.43 ml
- 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。
輸入產(chǎn)品批號:
本計算器可幫助您計算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關系,公式為:
質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)