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Plerixafor

Chemical Structure : Plerixafor

CAS No.: 110078-46-1

Plerixafor (JM-3100;AMD-3100;SID-791)

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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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

Physicochemical Properties

M.Wt 502.782
Formula C28H54N8
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

1,4,8,11-Tetraazacyclotetradecane, 1,1'-[1,4-phenylenebis(methylene)]bis-

References

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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