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BMS-707035

    99%

BMS-707035

源葉(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 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80920-5mg 99% ¥410.00元 10 - - -
源葉(MedMol) S80920-10mg 99% ¥800.00元 10 - - -
源葉(MedMol) S80920-50mg 99% ¥1800.00元 2 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

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)
產(chǎn)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)
靶點: HIV;HIV Integrase;HIVProtease
體內(nèi)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
參考文獻: 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)
保存條件: -20℃
配置溶液濃度參考:
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
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參考文獻

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