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TargetSphingosine 1-phosphate receptor 4
LigandBDBM50356255
Substrate/Competitorn/a
Meas. Tech.ChEMBL_774916 (CHEMBL1913361)
EC50 5400±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:
BDBM50356255
n/a
NameBDBM50356255
Synonyms:CHEMBL1910686
TypeSmall organic molecule
Emp. Form.C19H21FN4OS
Mol. Mass.372.46
SMILESCC\N=C1/S\C(=C/c2cc(C)n(c2C)-c2ncccc2F)C(=O)N1CC |(6.57,5.78,;7.33,4.44,;8.88,4.44,;9.79,3.2,;9.33,1.73,;10.58,.82,;10.59,-.72,;9.27,-1.49,;7.73,-1.5,;7.26,-2.96,;5.79,-3.44,;8.51,-3.87,;9.75,-2.96,;11.08,-3.73,;8.51,-5.41,;9.85,-6.18,;9.85,-7.73,;8.52,-8.5,;7.18,-7.73,;7.18,-6.18,;5.85,-5.41,;11.82,1.75,;13.29,1.29,;11.33,3.21,;12.23,4.46,;13.77,4.46,)|
Structure
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