DRV1 (GPR32) agonist C2A

Modify Date: 2024-01-15 00:48:04

DRV1 (GPR32) agonist C2A Structure
DRV1 (GPR32) agonist C2A structure
Common Name DRV1 (GPR32) agonist C2A
CAS Number 862811-76-5 Molecular Weight 364.348
Density 1.4±0.1 g/cm3 Boiling Point N/A
Molecular Formula C20H14F2N4O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of DRV1 (GPR32) agonist C2A


DRV1 (GPR32) agonist C2A (NCGC00135472) is a synthetic molecule that activate human resolvin D1 receptor DRV1/GPR32 receptor with EC50 of 0.37 uM and 0.05 uM in β-arrestin and cAMP assays, respectively; elicits rapid impedance changes in cells overexpressing recombinant DRV1, stimulates phagocytosis of serum-treated zymosan at concentrations comparable with that of RvD1, the endogenous DRV1 ligand, in human macrophages; also significantly increases by these chemotypes in DRV1-transfected macrophages in live E. coli.

 Names

Name 3,4-Difluoro-N-[3-(3-methylimidazo[1,2-a]pyrimidin-2-yl)phenyl]benzamide
Synonym More Synonyms

 DRV1 (GPR32) agonist C2A Biological Activity

Description DRV1 (GPR32) agonist C2A (NCGC00135472) is a synthetic molecule that activate human resolvin D1 receptor DRV1/GPR32 receptor with EC50 of 0.37 uM and 0.05 uM in β-arrestin and cAMP assays, respectively; elicits rapid impedance changes in cells overexpressing recombinant DRV1, stimulates phagocytosis of serum-treated zymosan at concentrations comparable with that of RvD1, the endogenous DRV1 ligand, in human macrophages; also significantly increases by these chemotypes in DRV1-transfected macrophages in live E. coli.
References References 1. Chiang N, et al. Cell Chem Biol. 2018 Nov 19. pii: S2451-9456(18)30383-0. View Related Products by Target Other Targets

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Molecular Formula C20H14F2N4O
Molecular Weight 364.348
Exact Mass 364.113556
LogP 3.72
Index of Refraction 1.654

 Synonyms

Benzamide, 3,4-difluoro-N-[3-(3-methylimidazo[1,2-a]pyrimidin-2-yl)phenyl]-
3,4-Difluoro-N-[3-(3-methylimidazo[1,2-a]pyrimidin-2-yl)phenyl]benzamide