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Reaction Details
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TargetLysophosphatidic acid receptor 2
LigandBDBM50233165
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1649786 (CHEMBL3998920)
EC50 3±n/a nM
Citation Banerjee, SNorman, DDLee, SCParrill, ALPham, TCBaker, DLTigyi, GJMiller, DD Highly Potent Non-Carboxylic Acid Autotaxin Inhibitors Reduce Melanoma Metastasis and Chemotherapeutic Resistance of Breast Cancer Stem Cells. J Med Chem60:1309-1324 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lysophosphatidic acid receptor 2
Name:Lysophosphatidic acid receptor 2
Synonyms:EDG4 | LPA receptor 2 | LPA-2 | LPA2 | LPAR2 | LPAR2_HUMAN | Lysophosphatidic acid receptor 2 | Lysophosphatidic acid receptor Edg-4
Type:PROTEIN
Mol. Mass.:39103.44
Organism:Homo sapiens (Human)
Description:ChEMBL_1451385
Residue:351
Sequence:
MVIMGQCYYNETIGFFYNNSGKELSSHWRPKDVVVVALGLTVSVLVLLTNLLVIAAIASN
RRFHQPIYYLLGNLAAADLFAGVAYLFLMFHTGPRTARLSLEGWFLRQGLLDTSLTASVA
TLLAIAVERHRSVMAVQLHSRLPRGRVVMLIVGVWVAALGLGLLPAHSWHCLCALDRCSR
MAPLLSRSYLAVWALSSLLVFLLMVAVYTRIFFYVRRRVQRMAEHVSCHPRYRETTLSLV
KTVVIILGAFVVCWTPGQVVLLLDGLGCESCNVLAVEKYFLLLAEANSLVNAAVYSCRDA
EMRRTFRRLLCCACLRQSTRESVHYTSSAQGGASTRIMLPENGHPLMDSTL
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  Blast E-value cutoff:
BDBM50233165
n/a
NameBDBM50233165
Synonyms:CHEMBL1222042
TypeSmall organic molecule
Emp. Form.C21H41O7P
Mol. Mass.436.5198
SMILESCCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)COP(O)(O)=O
Structure
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