Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetSphingosine 1-phosphate receptor 3
LigandBDBM50381896
Substrate/Competitorn/a
Meas. Tech.ChEMBL_817709 (CHEMBL2027357)
EC50>20000±n/a nM
Citation Asano, MNakamura, TSekiguchi, YMizuno, YYamaguchi, TTamaki, KShimozato, TDoi-Komuro, HKagari, TTomisato, WInoue, RYuita, HOguchi-Oshima, KKaneko, RNara, FKawase, YMasubuchi, NNakayama, SKoga, TNamba, ENasu, HNishi, T Synthesis and SAR of 1,3-thiazolyl thiophene and pyridine derivatives as potent, orally active and S1P3-sparing S1P1 agonists. Bioorg Med Chem Lett22:3083-8 (2012) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sphingosine 1-phosphate receptor 3
Name:Sphingosine 1-phosphate receptor 3
Synonyms:C9orf108 | C9orf47 | EDG3 | Endothelial differentiation G-protein coupled receptor 3 | S1P receptor 3 | S1P receptor Edg-3 | S1P3 | S1PR3 | S1PR3_HUMAN | Sphingosine 1-phosphate receptor | Sphingosine 1-phosphate receptor 3 (S1P3) | Sphingosine 1-phosphate receptor Edg-3
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:42278.13
Organism:Homo sapiens (Human)
Description:Q99500
Residue:378
Sequence:
MATALPPRLQPVRGNETLREHYQYVGKLAGRLKEASEGSTLTTVLFLVICSFIVLENLMV
LIAIWKNNKFHNRMYFFIGNLALCDLLAGIAYKVNILMSGKKTFSLSPTVWFLREGSMFV
ALGASTCSLLAIAIERHLTMIKMRPYDANKRHRVFLLIGMCWLIAFTLGALPILGWNCLH
NLPDCSTILPLYSKKYIAFCISIFTAILVTIVILYARIYFLVKSSSRKVANHNNSERSMA
LLRTVVIVVSVFIACWSPLFILFLIDVACRVQACPILFKAQWFIVLAVLNSAMNPVIYTL
ASKEMRRAFFRLVCNCLVRGRGARASPIQPALDPSRSKSSSSNNSSHSPKVKEDLPHTAP
SSCIMDKNAALQNGIFCN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50381896
n/a
NameBDBM50381896
Synonyms:CHEMBL2022914
TypeSmall organic molecule
Emp. Form.C26H31N3O3S
Mol. Mass.465.608
SMILESCCc1cc(ccc1OC(C)C)-c1cnc(s1)-c1ccc(CN2CC(C2)C(O)=O)nc1CC
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: