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DMU2105

    级别和纯度:
  • 10mM in DMSO
  • CAS编号: 1821143-79-6
  • 分子式: C18H13NO
  • 分子量: 259.30
有货

库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
D656801-1ml
1ml 期货 Stock Image

基本描述

规格或纯度 10mM in DMSO
英文名称 DMU2105
生化机理 DMU2105 是一种强效的特异性 CYP1B1 抑制剂,对 CYP1B1 和 CYP1A1 的 IC 50 s 分别为 10 nM 和 742 nM。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 抑制剂
产品介绍


DMU2105 is a potent and specific CYP1B1 inhibitor, with IC 50 s of 10 nM and 742 nM for CYP1B1 and CYP1A1, respectively.

In Vitro

DMU2105 (Compound 7k) shows 74 and 120-fold selectivity for CYP1B1 over CYP1A1 and CYP1A2. In the presence of DMU2105 however, the EC 50 goes down to 1 μM indicating that the cells have suffered from toxicity which may have been mediated by CYP1B1 inhibition. Un-transfected cells (HEK293: pcDNA3.1), when treated with cisplatin and DMU2105 (10×IC 50 ) do not show any perceptible decrease of cisplatin EC 50 (8.5 μM ± 0.9). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:CYP1B1 10 nM (IC 50 ) CYP1A1 742 nM (IC 50 )

关联靶点(人)

CYP1B1 Tchem 细胞色素 P450 1B1(Cytochrome P450 1B1) (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)
CYP1A1 Tchem 细胞色素 P450 1A1(Cytochrome P450 1A1) (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 C1=CC=C2C=C(C=CC2=C1)/C=C/C(=O)C3=CN=CC=C3
分子量 259.30
Reaxy-Rn 35887540
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=35887540&ln=

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
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