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Mizacorat

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 1893415-00-3
  • 分子式: C27H28F2N4O3
  • 分子量: 494.53
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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
M656113-1ml
1ml 期货 Stock Image

基本描述

别名 米萨科拉特
规格或纯度 10mM in DMSO
英文名称 Mizacorat
生化机理 Mizacorat(AZD9567;化合物 15)是一种强效的口服活性非甾体选择性糖皮质激素受体调节剂(SGRM),IC 50 为 3.8 nM。在链球菌细胞壁(SCW)再活化关节炎模型中表现出卓越的疗效
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 调节剂
产品介绍


Mizacorat (AZD9567; compound 15) is a potent, oral active, non-steroidal and selective glucocorticoid receptor modulator (SGRM) , with an IC 50 of 3.8 nM. Exhibits excellent efficacy in the streptococcal cell wall (SCW) reactivation model of joint inflammation

In Vivo

Mizacorat (15 mg/kg/day, Oral gavage daily for 8 days) treatment shows excellent in vivo efficacy in a rat model of joint inflammation . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Antigen-induced joint inflammation model in female Lewis rats (175-200 g), sensitized by an intra-articular injection of 5 μg of SCW . Dosage: 15 mg/kg/day. Administration: Oral gavage daily for 8 days. Result: Inhibited ankle swelling in the rat SCW model.

IC50& Target:IC50: 3.8 nM (Glucocorticoid receptor)

关联靶点(人)

NR3C1 Tclin 糖皮质激素受体(Glucocorticoid receptor) (0 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)
PGR Tclin 孕酮受体(Progesterone receptor) (0 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)
NR3C2 Tclin 盐皮质激素受体(Mineralocorticoid receptor) (0 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

Isomeric SMILES CC(C)[C@@H]([C@@H](C1=CC=CC=C1)OC2=CC3=C(C=C2)N(N=C3)C4=CN(C(=O)C=C4)C)NC(=O)C(C)(F)F
关联CAS 1893415-00-3
PubChem CID 121248172
MeSH Entry Terms AZD-9567;AZD9567
分子量 494.53

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