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TargetG-protein coupled receptor 4
LigandBDBM123511
Substrate/Competitorn/a
Meas. Tech.Radio Ligand Binding Assay
pH8±n/a
IC50 5±n/a nM
Citation Miltz, WOberhauser, BVaupel, AVelcicky, JWeigand, KLeleti, RRLiu, YDu, Z Pyrazolo pyrimidine derivatives US Patent US8748435 Publication Date 6/10/2014
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
G-protein coupled receptor 4
Name:G-protein coupled receptor 4
Synonyms:G-protein coupled receptor 4 | G-protein coupled receptor 4 (GPR4) | GPR4 | GPR4_HUMAN
Type:Enzyme
Mol. Mass.:40994.40
Organism:Homo sapiens (Human)
Description:P46093
Residue:362
Sequence:
MGNHTWEGCHVDSRVDHLFPPSLYIFVIGVGLPTNCLALWAAYRQVQQRNELGVYLMNLS
IADLLYICTLPLWVDYFLHHDNWIHGPGSCKLFGFIFYTNIYISIAFLCCISVDRYLAVA
HPLRFARLRRVKTAVAVSSVVWATELGANSAPLFHDELFRDRYNHTFCFEKFPMEGWVAW
MNLYRVFVGFLFPWALMLLSYRGILRAVRGSVSTERQEKAKIKRLALSLIAIVLVCFAPY
HVLLLSRSAIYLGRPWDCGFEERVFSAYHSSLAFTSLNCVADPILYCLVNEGARSDVAKA
LHNLLRFLASDKPQEMANASLTLETPLTSKRNSTAKAMTGSWAATPPSQGDQVQLKMLPP
AQ
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  Blast E-value cutoff:
BDBM123511
n/a
NameBDBM123511
Synonyms:US8748435, 36
TypeSmall organic molecule
Emp. Form.C25H30N6O
Mol. Mass.430.5453
SMILESCCc1nn2c(C)cc(C)nc2c1Cc1ccc(cc1)-c1nnc(o1)[C@H]1CC[C@H](N)CC1 |r,wU:25.28,wD:28.32,(-6.74,4.11,;-7.83,3.02,;-7.43,1.53,;-8.33,.29,;-7.43,-.96,;-7.75,-2.47,;-9.24,-2.86,;-6.6,-3.5,;-5.14,-3.02,;-4.05,-4.11,;-4.82,-1.51,;-5.96,-.48,;-5.96,1.06,;-4.63,1.83,;-3.3,1.06,;-3.3,-.48,;-1.96,-1.25,;-.63,-.48,;-.63,1.06,;-1.96,1.83,;.71,-1.25,;.71,-2.79,;2.17,-3.27,;3.08,-2.02,;2.17,-.78,;4.62,-2.02,;5.39,-.69,;6.93,-.69,;7.7,-2.02,;9.24,-2.02,;6.93,-3.36,;5.39,-3.36,)|
Structure
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