Chemical Structure : Plerixafor
CAS No.: 110078-46-1
Catalog No.: PC-42164Not For Human Use, Lab Use Only.
Plerixafor (JM-3100, AMD-3100, SID-791) is a potent, selective CXCR4 inhibitor (IC50=44 nM) that inhibits the replication of various HIV-1 and HIV-2 strains in various cell lines with EC50 of 10ng/ml.
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Plerixafor (JM-3100, AMD-3100, SID-791) is a potent, selective CXCR4 inhibitor (IC50=44 nM) that inhibits the replication of various HIV-1 and HIV-2 strains in various cell lines with EC50 of 10ng/ml; can produce mesenchymal stem cells and endothelial progenitor cells in mice in combination with VEGF; also is an allosteric agonist of CXCR7.
Blood Cancer
Approved
M.Wt | 502.782 | |
Formula | C28H54N8 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
1,4,8,11-Tetraazacyclotetradecane, 1,1'-[1,4-phenylenebis(methylene)]bis- |
1. Zabel BA, et al. J Immunol. 2009, 183(5), 3204-3211.
2. De Clercq E, et al. Antimicrob Agents Chemother. 1994 Apr;38(4):668-74.
3. Pitchford SC, et al. Cell Stem Cell. 2009 Jan 9;4(1):62-72.
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