Name | Israpafant |
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Description | Israpafant (Y-24180) is a potent, selective and long-acting platelet activation factor (PAF) receptor antagonist with IC50s of 0.84 nM and 3.84 nM against PAF-induced human and rabbit platelet aggregation, respectively. Israpafant stimulates both extracellular Ca2+ influx and intracellular Ca2+ release in prostate cancer cells. Israpafant suppresses the allergic cutaneous reactions including eosinophilia, cytokine production, edema and erythema in mice[1][2]. |
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Related Catalog | |
Target |
IC50: 0.84 nM (PAF-induced human platelet aggregation), 3.84 nM (PAF-induced rabbit platelet aggregation)[1] |
References |
Density | 1.26g/cm3 |
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Boiling Point | 637.3ºC at 760mmHg |
Molecular Formula | C28H29ClN4S |
Molecular Weight | 489.07 |
Flash Point | 339.2ºC |
Exact Mass | 488.18000 |
PSA | 71.31000 |
LogP | 6.62190 |
Vapour Pressure | 3.83E-16mmHg at 25°C |
Index of Refraction | 1.667 |