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1092776-63-0

中文名稱 1092776-63-0
英文名稱 CarbaMiMidothioic acid, N,N'-dicyclohexyl-, (5,6-dihydro-6,6-diMethyliMidazo[2,1-b]thiazol-3-yl)Methyl ester, hydrochloride (1:2)
CAS 1092776-63-0
分子式 C21H35ClN4S2
分子量 443.11
MOL 文件 1092776-63-0.mol
更新日期 2026/07/20 15:11:23
1092776-63-0 結構式 1092776-63-0 結構式

基本信息

中文別名
化合物IT1T二鹽酸鹽
化合物 T11693L
英文別名
IT1t dihydrochloride
N,N'-Dicyclohexylcarbamimidothioic acid (5,6-dihydro-6,6-dimethylimidazo[2,1-b]thiazol-3-yl)methyl ester dihydrochloride
CarbaMiMidothioic acid, N,N'-dicyclohexyl-, (5,6-dihydro-6,6-diMethyliMidazo[2,1-b]thiazol-3-yl)Methyl ester, hydrochloride (1
CarbaMiMidothioic acid, N,N'-dicyclohexyl-, (5,6-dihydro-6,6-diMethyliMidazo[2,1-b]thiazol-3-yl)Methyl ester, hydrochloride (1:2)
所屬類別
生物化工:抑制劑

物理化學性質

熔點>187° (dec.)
儲存條件Hygroscopic, -20°C Freezer, Under inert atmosphere
溶解度可溶于DMSO(少許)、甲醇(少許)
形態(tài)固體
顏色白色
化合物IT1T二鹽酸鹽價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/06/05HY-101458A化合物IT1T二鹽酸鹽
IT1t dihydrochloride
1092776-63-01 mg386元
2026/06/05HY-101458A1092776-63-0
IT1t dihydrochloride
1092776-63-05mg850元
2026/06/05HY-101458A1092776-63-0
IT1t dihydrochloride
1092776-63-010mM * 1mLin DMSO897元

常見問題列表

生物活性
IT1t dihydrochloride是高效的CXCR4拮抗劑;抑制CXCL12/CXCR4相互作用的IC50值為2.1 nM。
靶點

CXCL12/CXCR4

2.1 nM (IC 50 )

HIV-1 (X4)

14.2 nM (IC 50 , in MT-4 cells)

HIV-1 (X4)

19 nM (IC 50 , in PBMCs)

體外研究

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 IC 50 of 2.1 nM. This calcium flux is also inhibited by IT1t with an IC 50 of 23.1. 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 ? 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.

體內研究

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 .

"1092776-63-0" 相關產(chǎn)品信息
1092776-63-0 864677-55-4
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