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IT1t
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
IT1t图片
CAS NO:864677-55-4
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
IT1t是高效的CXCR4拮抗剂;抑制CXCL12/CXCR4相互作用的IC50值为2.1 nM。
生物活性

IT1t is a potentCXCR4antagonist; inhibits CXCL12/CXCR4 interaction with anIC50of 2.1 nM.

IC50& Target

CXCL12/CXCR4

2.1 nM (IC50)

HIV-1 (X4)

14.2 nM (IC50, in MT-4 cells)

HIV-1 (X4)

19 nM (IC50, in PBMCs)

体外研究
(In Vitro)

The CXCR4 is involved in chemotaxis and serves as a coreceptor for T-tropic HIV-1 viral entry and in cancer metastasis. IT1t is a small, drug-like, isothiourea derivative. IT1t shows very potent and dose-dependent inhibition of the CXCL12/CXCR4 interaction with an IC50of 2.1 nM. This calcium flux is also inhibited by IT1t with an IC50of 23.1[1]. Strong electron density is observed for IT1t in the binding cavity of both subunits of the CXCR4 homodimer. In dimers of CXCR4 bound to IT1t, the monomers interact only at the extracellular side of helices V and VI, leaving at least a 4 A gap between the intracellular regions, which is presumably filled by lipids. The IT1t compound and CVX15 peptide have both been characterized as competitive inhibitors of CXCL12, and many of the receptor-ligand contacts in the co-crystal structures presented are important for CXCL12 binding, including the acidic Asp187, Glu2887.39 and Asp972.63. The binding site of IT1t may point to the major anchor region for this domain[2].

体内研究
(In Vivo)

IT1t reduces the formation of TNBC early metastases in the zebrafish xenograft model. Tumor cell invasion at the metastatic site is effectively reduced upon CXCR4 silencing (Fig. 7B), similar to the antagonist IT1t[3].

分子量

406.65

Formula

C21H34N4S2

CAS 号

864677-55-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.