[CAS NO. 110078-46-1]  Plerixafor (AMD3100)

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PRODUCTS SPECIFICATIONS [110078-46-1]

Store
Catalog
SLK-S8030
Brand
Selleck
CAS
110078-46-1

DESCRIPTION [110078-46-1]

Overview

MDLMFCD05662218
Molecular Weight502.78
Molecular FormulaC28H54N8
SMILESC(C1=CC=C(CN2CCCNCCNCCCNCC2)C=C1)N3CCCNCCNCCCNCC3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM1.9889 mL9.9447 mL19.8894 mL
5 mM0.3978 mL1.9889 mL3.9779 mL
10 mM0.1989 mL0.9945 mL1.9889 mL
50 mM0.0398 mL0.1989 mL0.3978 mL

Description

Plerixafor (AMD3100, JM 3100, SID791) is a chemokine receptor antagonist for and -mediated chemotaxis with of 44 nM and 5.7 nM in cell-free assays, respectively. Plerixafor inhibits replication.

Targets

CXCL12 [1]
(Cell-free assay)
CXCR4 [1]
(Cell-free assay)
5.7 nM44 nM

In vitro

Plerixafor inhibits CXCL12-mediated chemotaxis with a potency lightly better than its affinity for CXCR4. Plerixafor also antagonizes SDF-1/CXCL12 ligand binding with an IC50 of 651 nM. Plerixafor inhibits SDF-1 mediated GTP-binding, SDF-1 mediated calcium flux and SDF-1 stimulated chemotaxis with IC50 of 27 nM, 572 nM and 51 nM, respectively. Plerixafor does not inhibit calcium flux against cells expressing CXCR3, CCR1, CCR2b, CCR4, CCR5 or CCR7 when stimulated with their cognate ligands, nor does Plerixafor inhibit receptor binding of LTB4. Plerixafor does not, on its own, induce a calcium flux in the CCRF–CEM cells, which express multiple GPCRs including CXCR4, CCR4 and CCR7.


Synonyms

1,4,8,11-Tetraazacyclotetradecane, 1,1′-[1,4-phenylenebis(methylene)]bis-
1,1′-[1,4-Phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane]
Plerixafor
Mozobil
JKL 169
1,1′-Xylyl bis-1.4,8,11 tetraaza cyclotetradecane
AMD 3100
SDZ SID 791
JM 3100
1-[[4-(1,4,8,11-Tetrazacyclotetradec-1-ylmethyl)phenyl]methyl]-1,4,8,11-tetrazacyclotetradecane