BMS-707035

    99%

BMS-707035

源叶(MedMol)
S80920
729607-74-3
C17H19FN4O5S
410.42
4-Pyrimidinecarboxamide, N-[(4-fluorophenyl)methyl]-1,6-dihydro-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-1,1-dioxido-2H-1,2-thiazin
品牌 货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
源叶(MedMol) S80920-5mg 99% ¥410.00元 10 - - -
源叶(MedMol) S80920-10mg 99% ¥800.00元 10 - - -
源叶(MedMol) S80920-50mg 99% ¥1800.00元 2 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

BMS-707035 is a potent orally active HIV-1 integrase strand transfer inhibitor (INSTI). BMS-707035 has enzyme inhibitory with an IC50 value of 3 nM. BMS-707035 also has weak CYP inhibiton and antiviral activity. BMS-707035 can be used for the research of human immunodeficiency virus-1 (HIV-1)
产品描述: BMS-707035 is a potent orally active HIV-1 integrase strand transfer inhibitor (INSTI). BMS-707035 has enzyme inhibitory with an IC50 value of 3 nM. BMS-707035 also has weak CYP inhibiton and antiviral activity. BMS-707035 can be used for the research of human immunodeficiency virus-1 (HIV-1)
靶点: HIV;HIV Integrase;HIVProtease
体内研究: BMS-707035 has a low clearance effect in the rat, dog and monkey with moderate to long elimination half-lives in all species
参考文献: 1. B Narasimhulu Naidu, et al. The discovery and preclinical evaluation of BMS-707035, a potent HIV-1 integrase strand transfer inhibitor. Bioorg Med Chem Lett. 2018 Jul 1;28(12):2124-2130.
溶解性: DMSO  :  50  mg/mL  (121.83  mM;  Need  ultrasonic)
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.437 ml 12.183 ml 24.365 ml
5 mM 0.487 ml 2.437 ml 4.873 ml
10 mM 0.244 ml 1.218 ml 2.437 ml
50 mM 0.049 ml 0.244 ml 0.487 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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