BDBM50496697 CHEMBL3218460

SMILES CCCCCCCCCCCCCCCC(=O)N[C@H](Cc1ccc(OCc2cc(OCC(F)(F)F)ccn2)cc1)\C=C\P(O)(O)=O

InChI Key InChIKey=PHXJFMYKLBONBN-QWXNGLIISA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50496697   

TargetLysophosphatidic acid receptor 1/3(Rattus norvegicus)
University Of Virginia

Curated by ChEMBL
LigandPNGBDBM50496697(CHEMBL3218460)
Affinity DataKi:  11nMAssay Description:Antagonist activity at LPAR1/LPAR3 in rat glioma C62B cells assessed as inhibition of LPA-induced reduction in isoproterenol-stimulated [3H]cAMP accu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysophosphatidic acid receptor 1(Homo sapiens (Human))
University Of Virginia

Curated by ChEMBL
LigandPNGBDBM50496697(CHEMBL3218460)
Affinity DataKi:  143nMAssay Description:Competitive antagonist activity at human LPA1 receptor overexpressed in CHO cells assessed as inhibition of LPA-induced [35S]GTPgammaS binding by liq...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLysophosphatidic acid receptor 3(Homo sapiens (Human))
University Of Virginia

Curated by ChEMBL
LigandPNGBDBM50496697(CHEMBL3218460)
Affinity DataKi:  512nMAssay Description:Competitive antagonist activity at N-terminal 3XHA-tagged human LPA3 receptor overexpressed in CHO cells assessed as inhibition of LPA-induced [35S]G...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed