Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetHydroxycarboxylic acid receptor 2
LigandBDBM50216550
Substrate/Competitorn/a
Meas. Tech.ChEMBL_479051 (CHEMBL921658)
IC50 4200±n/a nM
Citation Richman, JGKanemitsu-Parks, MGaidarov, ICameron, JSGriffin, PZheng, HGuerra, NCCham, LMaciejewski-Lenoir, DBehan, DPBoatman, DChen, RSkinner, POrnelas, PWaters, MGWright, SDSemple, GConnolly, DT Nicotinic acid receptor agonists differentially activate downstream effectors. J Biol Chem282:18028-36 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Hydroxycarboxylic acid receptor 2
Name:Hydroxycarboxylic acid receptor 2
Synonyms:G-protein coupled receptor 109A | G-protein coupled receptor HM74A | GPR109A | HCA2 | HCAR2 | HCAR2_HUMAN | HM74A | Hydroxycarboxylic acid receptor 2 | NIACR1 | Niacin Receptor GPR109A | Nicotinic acid receptor 1
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:41868.22
Organism:Homo sapiens (Human)
Description:Membranes from CHO cells expressing the recombinant human GPR109A were used in competition binding assay.
Residue:363
Sequence:
MNRHHLQDHFLEIDKKNCCVFRDDFIVKVLPPVLGLEFIFGLLGNGLALWIFCFHLKSWK
SSRIFLFNLAVADFLLIICLPFLMDNYVRRWDWKFGDIPCRLMLFMLAMNRQGSIIFLTV
VAVDRYFRVVHPHHALNKISNRTAAIISCLLWGITIGLTVHLLKKKMPIQNGGANLCSSF
SICHTFQWHEAMFLLEFFLPLGIILFCSARIIWSLRQRQMDRHAKIKRAITFIMVVAIVF
VICFLPSVVVRIRIFWLLHTSGTQNCEVYRSVDLAFFITLSFTYMNSMLDPVVYYFSSPS
FPNFFSTLINRCLQRKMTGEPDNNRSTSVELTGDPNKTRGAPEALMANSGEPWSPSYLGP
TSP
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50216550
n/a
NameBDBM50216550
Synonyms:3-(3-chlorobenzyl)-1H-pyrazole-5-carboxylic acid | 5-(3-Chloro-benzyl)-1H-pyrazole-3-carboxylic acid | 5-meta-chlorobenzyl-3-carboxyl-pyrazole | CHEMBL394441
TypeSmall organic molecule
Emp. Form.C11H9ClN2O2
Mol. Mass.236.654
SMILESOC(=O)c1cc(Cc2cccc(Cl)c2)[nH]n1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: