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TargetSphingosine 1-phosphate receptor 4
LigandBDBM50356264
Substrate/Competitorn/a
Meas. Tech.ChEMBL_774916 (CHEMBL1913361)
EC50 104±n/a nM
Citation Urbano, MGuerrero, MVelaparthi, SCrisp, MChase, PHodder, PSchaeffer, MTBrown, SRosen, HRoberts, E Discovery, synthesis and SAR analysis of novel selective small molecule S1P4-R agonists based on a (2Z,5Z)-5-((pyrrol-3-yl)methylene)-3-alkyl-2-(alkylimino)thiazolidin-4-one chemotype. Bioorg Med Chem Lett21:6739-45 (2011) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sphingosine 1-phosphate receptor 4
Name:Sphingosine 1-phosphate receptor 4
Synonyms:EDG6 | Endothelial differentiation G-protein coupled receptor 6 | S1P receptor 4 | S1P receptor Edg-6 | S1P4 | S1PR4 | S1PR4_HUMAN | Sphingosine 1-phosphate receptor | Sphingosine 1-phosphate receptor Edg-6 | Sphingosine-1-phosphate receptor 4 | sphingosine-1-phosphate 4 S1P4
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:41647.39
Organism:Homo sapiens (Human)
Description:n/a
Residue:384
Sequence:
MNATGTPVAPESCQQLAAGGHSRLIVLHYNHSGRLAGRGGPEDGGLGALRGLSVAASCLV
VLENLLVLAAITSHMRSRRWVYYCLVNITLSDLLTGAAYLANVLLSGARTFRLAPAQWFL
REGLLFTALAASTFSLLFTAGERFATMVRPVAESGATKTSRVYGFIGLCWLLAALLGMLP
LLGWNCLCAFDRCSSLLPLYSKRYILFCLVIFAGVLATIMGLYGAIFRLVQASGQKAPRP
AARRKARRLLKTVLMILLAFLVCWGPLFGLLLADVFGSNLWAQEYLRGMDWILALAVLNS
AVNPIIYSFRSREVCRAVLSFLCCGCLRLGMRGPGDCLARAVEAHSGASTTDSSLRPRDS
FRGSRSLSFRMREPLSSISSVRSI
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  Blast E-value cutoff:
BDBM50356264
n/a
NameBDBM50356264
Synonyms:CHEMBL1910800
TypeSmall organic molecule
Emp. Form.C20H21F2N3OS
Mol. Mass.389.462
SMILESCC\N=C1/S\C(=C/c2cc(C)n(c2C)-c2ccc(F)cc2F)C(=O)N1CC |(23.57,-28.17,;24.34,-29.51,;25.88,-29.51,;26.8,-30.75,;26.33,-32.22,;27.58,-33.13,;27.6,-34.67,;26.27,-35.44,;24.73,-35.45,;24.26,-36.91,;22.79,-37.39,;25.51,-37.82,;26.75,-36.91,;28.08,-37.68,;25.51,-39.36,;24.18,-40.13,;24.19,-41.66,;25.52,-42.43,;25.53,-43.97,;26.86,-41.65,;26.85,-40.11,;28.18,-39.33,;28.82,-32.2,;30.29,-32.66,;28.34,-30.74,;29.23,-29.49,;30.77,-29.49,)|
Structure
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