CAS NO: | 1194961-19-7 |
包装 | 价格(元) |
10 mM * 1 mL in Water | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | PRT-060318 (PRT318) is a novel selective inhibitor of the tyrosine kinaseSykwith anIC50of 4 nM. | ||||||||||||||||
IC50& Target | IC50: 4 nM (Syk)[1] | ||||||||||||||||
体外研究 (In Vitro) | PRT318 is a potent inhibitor of purified Syk kinase with an IC50of 4 nM. Syk kinase is inhibited by 92%, whereas all other kinases retains more than 70% at a concentration of 50 nM of PRT318[1]. PRT318 and P505-15 effectively antagonize CLL cell survival after B-cell receptor (BCR) triggering and in nurse-like cell-co-cultures. They inhibit BCR-dependent secretion of the chemokines CCL3 and CCL4 by CLL cells, and leukemia cell migration toward the tissue homing chemokines CXCL12, CXCL13, and beneath stromal cells. PRT318 and P505-15 inhibit Syk and extracellular signal-regulated kinase phosphorylation after BCR triggering[2]. | ||||||||||||||||
体内研究 (In Vivo) | PRT318 completely inhibits HIT immune complex-induced aggregation of both human and transgenic HIT mouse platelets. Pretreatment of mice with PRT318 markedly reduces HIT IC-induced thrombosis in the lungs. The Thrombosis Score is significantly lower for PRT318-treated mice compared with control[1]. | ||||||||||||||||
分子量 | 340.42 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H24N6O | ||||||||||||||||
CAS 号 | 1194961-19-7 | ||||||||||||||||
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: H2O : 5.6 mg/mL(16.45 mM;Need ultrasonic and warming) 配制储备液
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