RQ-00311651结构式
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常用名 | RQ-00311651 | 英文名 | RQ-00311651 |
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CAS号 | 1257116-00-9 | 分子量 | 405.374 | |
密度 | 1.4±0.1 g/cm3 | 沸点 | 655.8±55.0 °C at 760 mmHg | |
分子式 | C19H18F3N5O2 | 熔点 | N/A | |
MSDS | N/A | 闪点 | 350.4±31.5 °C |
RQ-00311651用途RQ-00311651 is a novel T-type Ca2+ channel blocker, in distinct rodent models for neuropathic and visceral pain. RQ-00311651 strongly suppressed T currents when tested at holding potentials of -65 ~ -60 mV, but not -80 mV, in the Cav3.1- or Cav3.2-expressing cells. RQ-00311651 also inhibited high K-induced Ca signaling in those cells. |
英文名 | (1S,2S)-2-(1H-Benzimidazol-2-yl)-N-{(1R)-1-[5-(2,2,2-trifluoroethoxy)-2-pyrazinyl]ethyl}cyclopropanecarboxamide |
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英文别名 | 更多 |
密度 | 1.4±0.1 g/cm3 |
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沸点 | 655.8±55.0 °C at 760 mmHg |
分子式 | C19H18F3N5O2 |
分子量 | 405.374 |
闪点 | 350.4±31.5 °C |
精确质量 | 405.141266 |
LogP | 1.63 |
蒸汽压 | 0.0±2.0 mmHg at 25°C |
折射率 | 1.609 |
(1S,2S)-2-(1H-Benzimidazol-2-yl)-N-{(1R)-1-[5-(2,2,2-trifluoroethoxy)-2-pyrazinyl]ethyl}cyclopropanecarboxamide |
Cyclopropanecarboxamide, 2-(1H-benzimidazol-2-yl)-N-[(1R)-1-[5-(2,2,2-trifluoroethoxy)-2-pyrazinyl]ethyl]-, (1S,2S)- |