BMS-191011

CAS号

202821-81-6

分子式

C16H10ClF3N2O3

主要靶点

Potassium Channel

仅限科研使用

Cat No : CM06071

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Synonyms

IGR39|inhibit|BMS 191011|BMS-A|BMS191011|BMS-191011|Inhibitor|KcsA|neuroprotective activity|Panc-1|PotassiumChannel|Potassium Channel|rodent models of stroke



产品信息

CAS号 202821-81-6
分子式 C16H10ClF3N2O3
主要靶点 Potassium Channel
主要通路 离子通道
分子量 370.71
纯度 97.43%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
别名 IGR39|inhibit|BMS 191011|BMS-A|BMS191011|BMS-191011|Inhibitor|KcsA|neuroprotective activity|Panc-1|PotassiumChannel|Potassium Channel|rodent models of stroke

体内活性

在活体内,BMS 191011(10-100 μg/kg,静脉注射)能够增加大鼠视网膜动脉的直径,而不影响血压或心率,这一效果可被BKCa通道阻断剂iberiotoxin[1]逆转。

溶解度

DMSO:125 mg/mL (337.19 mM)

参考文献

1.Mori A , Suzuki S , Sakamoto K , et al. BMS-191011, an Opener of Large-Conductance Ca2+-Activated Potassium Channels, Dilates Rat Retinal Arterioles in Vivo[J]. Biological & Pharmaceutical Bulletin, 2011, 34(1):150-152.
2.Hewawasam P . Synthesis of water-soluble prodrugs of BMS-191011: a maxi-K channel opener targeted for post-stroke neuroprotection.[J]. Bioorganic & Medicinal Chemistry Letters, 2003, 13(10):1695-1698.

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