
LIT-927
CAS No. 2172879-52-4
LIT-927( LIT927 )
Catalog No. M13474 CAS No. 2172879-52-4
LIT-927 (LIT927) is the first selective, locally and orally active CXCL12 neutraligand with Ki of 267 nM for CXCL12-TR binding inhibition.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 41 | In Stock |
![]() ![]() |
5MG | 63 | In Stock |
![]() ![]() |
10MG | 101 | In Stock |
![]() ![]() |
25MG | 194 | In Stock |
![]() ![]() |
50MG | 312 | In Stock |
![]() ![]() |
100MG | 524 | In Stock |
![]() ![]() |
500MG | 1143 | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameLIT-927
-
NoteResearch use only, not for human use.
-
Brief DescriptionLIT-927 (LIT927) is the first selective, locally and orally active CXCL12 neutraligand with Ki of 267 nM for CXCL12-TR binding inhibition.
-
DescriptionLIT-927 (LIT927) is the first selective, locally and orally active CXCL12 neutraligand with Ki of 267 nM for CXCL12-TR binding inhibition; displays excellent selectivity over other chemokines (CCL17, CCL22, CCL5 and CCL2), inhibits the increase in intracellular calcium concentration in EGFP-CXCR4+HEK cells in response to CXCL12 at 10 uM, has no effect on calcium responses triggered by either CCL17 or CCL22 on EGFP-CCR4+HEK cells, CCL5 on EGFP-CCR5+ HEK cells, or by CCL2 on EGFP-CCR2+HEK cells; reduces eosinophil recruitment in murine model of allergic airway hypereosinophilia.
-
In Vitro——
-
In Vivo——
-
SynonymsLIT927
-
PathwayGPCR/G Protein
-
TargetChemokine Receptor
-
RecptorCXCL12
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2172879-52-4
-
Formula Weight328.752
-
Molecular FormulaC17H13ClN2O3
-
Purity>98% (HPLC)
-
SolubilityDMSO: 25 mg/mL, 76.05 mM; Water: Insoluble ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESO=C1N=C(C2=CC=C(Cl)C=C2)C=C(C3=CC=C(O)C(OC)=C3)N1
-
Chemical Name4-(4-Chlorophenyl)-6-(4-hydroxy-3-methoxyphenyl)pyrimidin-2(1H)-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Regenass P, et al. J Med Chem. 2018 Aug 28. doi: 10.1021/acs.jmedchem.8b00657.
molnova catalog



related products
-
GSK812397
GSK812397 is a potent, selective, noncompetitive, orally available antagonist of CXCR4 receptor.
-
MLN 3897
MLN 3897 is a potent, specific and orally active antagonist of CCR1 with IC50 of 0.8 nM in competition binding assays.
-
Vicriviroc maleate
A potent, highly selective, and orally bioavailable CCR5 antagonist with Ki of 2.5 nM.