Chemical Structure : HF50731
Catalog No.: PC-72032Not For Human Use, Lab Use Only.
HF50731 (HF-50731) is a novel potent, selective CXCR4 antagonist with Ki of 19.8 nM in the CXCR4 competitive binding assay.
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HF50731 (HF-50731) is a novel potent, selective CXCR4 antagonist with Ki of 19.8 nM in the CXCR4 competitive binding assay.
HF50731 significantly inhibited SDF-1α-induced calcium mobilization (IC50=621 nM) and cell migration, and blocked HIV-1 infection via antagonizing CXCR4 coreceptor function (IC50=1.5 uM).
The structure-activity relationship analysis demonstrated that HF50731 could primarily occupy the minor subpocket of CXCR4 and partially bind in the major subpocket by interacting with residues W94, D97, D171, and E288.
M.Wt | 414.682 | |
Formula | C26H46N4 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Xiong Fang, et al. Eur J Med Chem. 2020 Aug 15;200:112410.
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