S80510 |
PD 168393 |
源葉(MedMol) | 98% |
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- 產(chǎn)品描述: PD168393 is a potent, selective and cell-permeable inhibitor of EGFR tyrosine kinase and ErbB2. PD168393 irreversiblely inactivates EGF receptor ( IC50=0.7 nM) and is inactive against insulin receptor, PDGFR, FGFR and PKC
- 靶點(diǎn): EGFR:0.7 nM (IC50);Apoptosis;EGFR;FGFR;IGF-1R;PDGFR;PKC;Autophagy
- 體內(nèi)研究:
PD168393 (intraperitoneal injection; 58 mg/kg; once daily; days 10-14, 17-21, and 24-28) is effective in vivo, and produces tumor growth inhibition of 115% after 15 days’ treatment in human epidermoid carcinoma xenografts in mice
- 參考文獻(xiàn):
1. D W Fry, et al. Specific, irreversible inactivation of the epidermal growth factor receptor and erbB2, by a new class of tyrosine kinase inhibitor. Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):12022-7.
- 溶解性: DMSO : ≥ 30 mg/mL (81.25 mM)
- 保存條件: RT
- 配置溶液濃度參考:
1mg 5mg 10mg 1 mM 2.708 ml 13.542 ml 27.084 ml 5 mM 0.542 ml 2.708 ml 5.417 ml 10 mM 0.271 ml 1.354 ml 2.708 ml 50 mM 0.054 ml 0.271 ml 0.542 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(quán)威性,僅供客戶參考交流研究之用。
輸入產(chǎn)品批號:
本計(jì)算器可幫助您計(jì)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(guān)系,公式為:
質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)