Plerixafor
CAS No. 110078-46-1
Plerixafor( JM-3100 | AMD-3100 | SID-791 )
Catalog No. M10387 CAS No. 110078-46-1
Plerixafor (JM-3100, AMD-3100, SID-791) is a potent, selective CXCR4 inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 38 | In Stock |
|
| 10MG | 57 | In Stock |
|
| 25MG | 102 | In Stock |
|
| 50MG | 161 | In Stock |
|
| 100MG | 291 | In Stock |
|
| 200MG | 462 | In Stock |
|
| 500MG | 736 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePlerixafor
-
NoteResearch use only, not for human use.
-
Brief DescriptionPlerixafor (JM-3100, AMD-3100, SID-791) is a potent, selective CXCR4 inhibitor.
-
DescriptionPlerixafor (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.
-
In Vitro——
-
In Vivo——
-
SynonymsJM-3100 | AMD-3100 | SID-791
-
PathwayGPCR/G Protein
-
TargetChemokine Receptor
-
RecptorCXCL12|CXCR4
-
Research AreaCancer
-
IndicationBlood cancer
Chemical Information
-
CAS Number110078-46-1
-
Formula Weight502.782
-
Molecular FormulaC28H54N8
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESC1(CN2CCNCCCNCCNCCC2)=CC=C(CN3CCNCCCNCCNCCC3)C=C1
-
Chemical Name1,4,8,11-Tetraazacyclotetradecane, 1,1'-[1,4-phenylenebis(methylene)]bis-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
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.
molnova catalog
related products
-
IT1t
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.
-
CX 4338
CX 4338 (CX4338, CX-4338)?is a potent, selective CXCR2 inhibitor that selectively inhibits CXCR2-mediated recruitment of β-arrestin-2 with IC50 of 6.3 uM.
-
INCB10820
INCB10820 (PF-4178903) is a potent, selective, orally bioavailable dual CCR2 and CCR5 antagonist with binding IC50 of 3.0 nM and 5.3 nM, respectively.
Cart
sales@molnova.com