CAS NO: | 1429639-50-8 |
生物活性 | CZ415 is a potent and highly selectivemTORinhibitor with apIC50of 8.07. CZ415 inhibitsmTORC1andmTORC2protein complex. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Inhibition of phosphorylation for both downstream targets results in 14.5 nM IC50for pS6RP and 14.8 nM for pAKT. The immunosuppressive effect of CZ415 is measured by detecting secreted IFNγ after 18 hours in stimulated human whole blood and the resulting IC50is 226 nM. As a predictor for cardiotoxicity, the activity of CZ415 against the human cardiac ion channel hERG is assessed in a whole-cell patch-clamp assay in HEK293 cells resulting in an IC50of 48 μM[1]. | ||||||||||||||||
体内研究 (In Vivo) | CZ415 is a highly selective mTOR inhibitor showing in vivo efficacy in a collagen induced arthritis (CIA) model. For full characterization of CZ415 and to enable improved dose predictions, the pharmacokinetic (PK) profile is assessed in rat. PK and oral bioavailability are determined after of 1 mg/kg intravenous (iv) bolus and 3 mg/kg oral (po) administration. The observed plasma clearance, corresponding to 45% liver blood flow, suggests that sufficient levels of free compound are circulating in the animal over time. The oral uptake is rapid with a Tmaxmax of 0.5 h and bioavailability F = 44% indicates very good absorption from the gut[1]. | ||||||||||||||||
分子量 | 459.56 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H29N5O4S | ||||||||||||||||
CAS 号 | 1429639-50-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 100 mg/mL(217.60 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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