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SCH-1473759 hydrochloride

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 1094067-13-6
  • 分子式: C20H27ClN8OS
  • 分子量: 463.00
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
S654936-1ml
1ml 期货 Stock Image

基本描述

别名 SCH-1473759 盐酸盐
规格或纯度 10mM in DMSO
英文名称 SCH-1473759 hydrochloride
生化机理 SCH-1473759 盐酸盐是一种极光抑制剂,对极光 A 和极光 B 的 IC 50 s 分别为 4 和 13 nM。
储存温度 干燥,-80℃储存
运输条件 超低温冰袋运输
产品介绍


SCH-1473759 hydrochloride is an aurora inhibitor with IC 50 s of 4 and 13 nM for aurora A and B, respectively.

In Vitro

SCH-1473759 directly binds to aurora A and B with K d s of 20 and 30 nM, respectively. SCH-1473759 also inhibits the Src family of kinases (IC 50 <10 nM), Chk1 (IC 50 =13 nM), VEGFR2 (IC 50 =1 nM), and IRAK4 (IC 50 =37 nM). It does not have significant activity (IC 50 >1000 nM) against 34 other kinases representing different families of the kinome. SCH-1473759 inhibits HCT116 cells proliferation with an IC 50 of 6 nM. SCH 1473759 inhibits tumor cell lines from different tissues (breast, ovarian, prostate, lung, colon, brain, gastric, renal, skin, and leukemia). The most sensitive cell lines includ A2780, LNCap, N87, Molt4, K562, and CCRF-CEM with IC 50 values <5 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

SCH-1473759 at a low dose of 5 mg/kg (ip, bid) is well-tolerated in a continuous dosing schedule and shows 50% tumor growth inhibition(TGI) on day 16. A higher dose of 10mg/kg(ip, bid) is well-tolerated in an intermittent schedule (5 days on, 5 days off) and gave 69% TGI on day 16. SCH-1473759 shows good exposure in all species with the clearance being high in rodents and moderate in dog and monkey. The half-life is also moderate, but the tissue distribution is high . SCH 1473759 dose- and schedule-dependent anti-tumor activity in four human tumor xenograft models. Further, the efficacy is enhanced in combination with taxanes and found to be most efficacious when SCH 1473759 is dosed 12-h post-taxane treatment. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal administration

Mice: Anti-tumor efficacy of SCH 1473759 dosed i.p. is evaluated in mice bearing established A2780 ovarian tumor xenografts. Three schedules are tested at their respective maximum tolerated doses: 10 mg/kg bid (twice daily), 20 mg/kg qd (daily), and 100 mg/kg day 0, 4, 7. Additionally, 60 mg/kg day 0, 4, 7 is tested . aladdin has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:Aurora A 4 nM (IC 50 ) Aurora B 13 nM (IC 50 )

关联靶点(人)

IRAK4 Tchem 白细胞介素-1受体相关激酶4(Interleukin-1 receptor-associated kinase 4) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
FLT3 Tclin 受体型酪氨酸蛋白激酶 FLT3(Receptor-type tyrosine-protein kinase FLT3) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
AURKB Tchem 极光激酶B(Aurora kinase B) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
CHEK1 Tchem 丝氨酸/苏氨酸蛋白激酶 Chk1(Serine/threonine-protein kinase Chk1) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

分子类型 小分子
Isomeric SMILES CCN(CC1=NSC(=C1)NC2=NC(=CN3C2=NC=C3C4=CNN=C4)C)C(C)(C)CO.Cl
PubChem CID 53317913
分子量 463.00

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