Reaction Details |
| Report a problem with these data |
Target | Sphingosine 1-phosphate receptor 5 |
---|
Ligand | BDBM50169454 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_304309 (CHEMBL830104) |
---|
EC50 | 29±n/a nM |
---|
Citation | Clemens, JJ; Davis, MD; Lynch, KR; Macdonald, TL Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: discovery of potent S1P1 receptor agonists. Bioorg Med Chem Lett15:3568-72 (2005) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Sphingosine 1-phosphate receptor 5 |
---|
Name: | Sphingosine 1-phosphate receptor 5 |
Synonyms: | EDG8 | Endothelial differentiation sphingolipid G-protein-coupled receptor 8 | S1P5 | S1PR5 | S1PR5_HUMAN | Sphingosine 1-phosphate receptor | Sphingosine 1-phosphate receptor Edg-8 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 41796.42 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 398 |
Sequence: | MESGLLRPAPVSEVIVLHYNYTGKLRGARYQPGAGLRADAVVCLAVCAFIVLENLAVLLV
LGRHPRFHAPMFLLLGSLTLSDLLAGAAYAANILLSGPLTLKLSPALWFAREGGVFVALT
ASVLSLLAIALERSLTMARRGPAPVSSRGRTLAMAAAAWGVSLLLGLLPALGWNCLGRLD
ACSTVLPLYAKAYVLFCVLAFVGILAAICALYARIYCQVRANARRLPARPGTAGTTSTRA
RRKPRSLALLRTLSVVLLAFVACWGPLFLLLLLDVACPARTCPVLLQADPFLGLAMANSL
LNPIIYTLTNRDLRHALLRLVCCGRHSCGRDPSGSQQSASAAEASGGLRRCLPPGLDGSF
SGSERSSPQRDGLDTSGSTGSPGAPTAARTLVSEPAAD
|
|
|
BDBM50169454 |
---|
n/a |
---|
Name | BDBM50169454 |
Synonyms: | CHEMBL188826 | Thiophosphoric acid (R)-2-amino-2-[5-(4-octyl-phenyl)-1H-imidazol-2-yl]-ethyl ester; TFA |
Type | Small organic molecule |
Emp. Form. | C19H30N3O3PS |
Mol. Mass. | 411.499 |
SMILES | CCCCCCCCc1ccc(cc1)-c1c[nH]c(n1)[C@@H](N)COP(O)(O)=S |
Structure |
|