Reaction Details |
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Target | Hydroxycarboxylic acid receptor 2 |
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Ligand | BDBM50211362 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_449367 (CHEMBL899634) |
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EC50 | >1000±n/a nM |
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Citation | Skinner, PJ; Cherrier, MC; Webb, PJ; Shin, YJ; Gharbaoui, T; Lindstrom, A; Hong, V; Tamura, SY; Dang, HT; Pride, CC; Chen, R; Richman, JG; Connolly, DT; Semple, G Fluorinated pyrazole acids are agonists of the high affinity niacin receptor GPR109a. Bioorg Med Chem Lett17:5620-3 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Hydroxycarboxylic acid receptor 2 |
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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
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BDBM50211362 |
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n/a |
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Name | BDBM50211362 |
Synonyms: | 5-methyl-1H-pyrazole-3-carboxylic acid | 5-methyl-3-carboxyl-pyrazole | 5-methylpyrazole-3-carboxylic acid | CHEMBL391574 |
Type | Small organic molecule |
Emp. Form. | C5H6N2O2 |
Mol. Mass. | 126.1133 |
SMILES | Cc1cc(n[nH]1)C(O)=O |
Structure |
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