
IT1t
CAS No. 864677-55-4
IT1t( Isothiourea 1t )
Catalog No. M16271 CAS No. 864677-55-4
A highly potent, selective, orally bioavailable CXCR4 inhibitor with binding IC50 of 8 nM for hCXCR4, IC50 of 1.1 nM in Ca2+-mobilization assays.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 873 | Get Quote |
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50MG | 1782 | Get Quote |
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100MG | 2250 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameIT1t
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NoteResearch use only, not for human use.
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Brief DescriptionA highly potent, selective, orally bioavailable CXCR4 inhibitor with binding IC50 of 8 nM for hCXCR4, IC50 of 1.1 nM in Ca2+-mobilization assays.
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DescriptionA highly potent, selective, orally bioavailable CXCR4 inhibitor with binding IC50 of 8 nM for hCXCR4, IC50 of 1.1 nM in Ca2+-mobilization assays; inhibits HIV-1IIIB attachment with IC50 of 7 nM, and IC90 of 100 nM; also show promising anti-tumor effects, impairs the formation of TNBC early metastases in a zebrafish xenograft model.
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In VitroThe 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 IC50 of 2.1 nM. This calcium flux is also inhibited by IT1t with an IC50 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.
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In VivoIT1t 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 .
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SynonymsIsothiourea 1t
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PathwayGPCR/G Protein
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TargetChemokine Receptor
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RecptorChemokine Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number864677-55-4
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Formula Weight406.65146
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Molecular FormulaC21H34N4S2
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Purity>98% (HPLC)
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SolubilityDMSO
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SMILESCC1(CN2C(=CSC2=N1)CSC(=NC3CCCCC3)NC4CCCCC4)C
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Chemical NameCarbamimidothioic acid, N,N'-dicyclohexyl-, (5,6-dihydro-6,6-dimethylimidazo[2,1-b]thiazol-3-yl)methyl ester
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Wu B, et al. Science. 2010 Nov 19;330(6007):1066-71.
2. Thoma G, et al. J Med Chem. 2008 Dec 25;51(24):7915-20.
3. Das D, et al. Antimicrob Agents Chemother. 2015 Apr;59(4):1895-904.
4. Tulotta C, et al. Dis Model Mech. 2016 Feb;9(2):141-53.
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