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TargetLysophosphatidic acid receptor 1
LigandBDBM50211647
Substrate/Competitorn/a
Meas. Tech.ChEMBL_455638 (CHEMBL903636)
IC50 56±n/a nM
Citation Yamamoto, TFujita, KAsari, SChiba, AKataba, YOhsumi, KOhmuta, NIida, YIjichi, CIwayama, SFukuchi, NShoji, M Synthesis and evaluation of isoxazole derivatives as lysophosphatidic acid (LPA) antagonists. Bioorg Med Chem Lett17:3736-40 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lysophosphatidic acid receptor 1
Name:Lysophosphatidic acid receptor 1
Synonyms:Edg2 | Gpcr91 | LPAR1_RAT | Lpa1 | Lpar1 | Lysophosphatidic acid receptor 1/lysophosphatidic acid receptor 3 | Lysophosphatidic acid receptor Edg-2
Type:PROTEIN
Mol. Mass.:41130.42
Organism:Rattus norvegicus
Description:ChEMBL_329844
Residue:364
Sequence:
MAAASTSSPVISQPQFTAMNEQQCFYNESIAFFYNRSGKYLATEWNTVSKLVMGLGITVC
VFIMLANLLVMVAIYVNRRFHFPIYYLMANLAAADFFAGLAYFYLMFNTGPNTRRLTVST
WLLRQGLIDTSLTASVANLLAIAIERHITVFRMQLHTRMSNRRVVVVIVVIWTMAIVMGA
IPSVGWNCICDIDHCSNMAPLYSDSYLVFWAIFNLVTFVVMVVLYAHIFGYVRQRTMRMS
RHSSGPRRNRDTMMSLLKTVVIVLGAFIVCWTPGLVLLLLDVCCPQCDVLAYEKFFLLLA
EFNSAMNPIIYSYRDKEMSATFRQILCCQRNENPNGPTEGSDRSASSLNHTILAGVHSND
HSVV
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  Blast E-value cutoff:
BDBM50211647
n/a
NameBDBM50211647
Synonyms:3-(4-(4-((1-(2-chlorocyclohex-1-enyl)ethoxy)carbonyl)isoxazol-3-yl)benzylthio)propanoic acid | CHEMBL246943
TypeSmall organic molecule
Emp. Form.C22H25ClN2O5S
Mol. Mass.464.962
SMILESCC(OC(=O)Nc1conc1-c1ccc(CSCCC(O)=O)cc1)C1=C(Cl)CCCC1 |c:26|
Structure
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