
POL3026
CAS No. 918660-21-6
POL3026( POL 3026 | POL-3026 )
Catalog No. M16597 CAS No. 918660-21-6
A highly potent, selective beta-hairpin mimetic CXCR4 inhibitor with IC50 of 1.2 nM in Ca2+ flux assay.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
100MG | Get Quote | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NamePOL3026
-
NoteResearch use only, not for human use.
-
Brief DescriptionA highly potent, selective beta-hairpin mimetic CXCR4 inhibitor with IC50 of 1.2 nM in Ca2+ flux assay.
-
DescriptionA highly potent, selective beta-hairpin mimetic CXCR4 inhibitor with IC50 of 1.2 nM in Ca2+ flux assay; shows excellent plasma stability, high selectivity for CXCR4, favorable pharmacokinetic properties in vivo, has the potential to become a therapeutic compound for application in the treatment of HIV infections (as an entry inhibitor), cancer (for angiogenesis suppression and inhibition of metastasis), inflammation, and in stem cell transplant therapy.HIV Infection Discontinued.
-
In Vitro——
-
In Vivo——
-
SynonymsPOL 3026 | POL-3026
-
PathwayGPCR/G Protein
-
TargetChemokine Receptor
-
RecptorChemokine Receptor
-
Research AreaInfection
-
IndicationHIV Infection
Chemical Information
-
CAS Number918660-21-6
-
Formula Weight——
-
Molecular Formula——
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical NameCyclo[3-(2-naphthalenyl)-L-alanyl-L-cysteinyl-L-tyrosyl-L-glutaminyl-L-lysyl-D-prolyl-L-prolyl-L-tyrosyl-L-arginyl-N5-(aminocarbonyl)-L-ornithyl-L-cysteinyl-L-arginylglycyl-D-prolyl-L-arginyl-L-arginyl], cyclic (2?1)-disulfide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. DeMarco SJ, et al. Bioorg Med Chem. 2006 Dec 15;14(24):8396-404.
2. Moncunill G, et al. Mol Pharmacol. 2008 Apr;73(4):1264-73.
3. Lesniak WG, et al. Mol Pharm. 2015 Mar 2;12(3):941-53.
molnova catalog



related products
-
KRH-1636
A potent, selective inhibitor of CXCR4 with IC50 of 13 nM.
-
AZD 5069
AZD 5069 (AZD5069)?is a potent, selective, slowly reversible and orally bioavailable CXCR2 antagonist that inhibits CXCL8 binding to CXCR2 with pIC50 of 9.1.
-
BX471
BX471 is a potent, selective, non-peptide CCR1 antagonist with Ki of 1 nM for hCCR1, displays 100 times less affinity for rat CCR1.