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TargetNeuropeptides B/W receptor type 1
LigandBDBM75925
Substrate/Competitorn/a
Meas. Tech.ChEMBL_887068 (CHEMBL2213859)
IC50 12200±n/a nM
Citation Urbano, MGuerrero, MZhao, JVelaparthi, SSaldanha, SAChase, PWang, ZCivelli, OHodder, PSchaeffer, MTBrown, SRosen, HRoberts, E Design, synthesis and SAR analysis of novel potent and selective small molecule antagonists of NPBWR1 (GPR7). Bioorg Med Chem Lett22:7135-41 (2012) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuropeptides B/W receptor type 1
Name:Neuropeptides B/W receptor type 1
Synonyms:GPR7 | NPBW1_HUMAN | NPBWR1 | neuropeptides B/W receptor 1
Type:Enzyme Catalytic Domain
Mol. Mass.:36111.82
Organism:Homo sapiens (Human)
Description:gi_119607128
Residue:328
Sequence:
MDNASFSEPWPANASGPDPALSCSNASTLAPLPAPLAVAVPVVYAVICAVGLAGNSAVLY
VLLRAPRMKTVTNLFILNLAIADELFTLVLPINIADFLLRQWPFGELMCKLIVAIDQYNT
FSSLYFLTVMSADRYLVVLATAESRRVAGRTYSAARAVSLAVWGIVTLVVLPFAVFARLD
DEQGRRQCVLVFPQPEAFWWRASRLYTLVLGFAIPVSTICVLYTTLLCRLHAMRLDSHAK
ALERAKKRVTFLVVAILAVCLLCWTPYHLSTVVALTTDLPQTPLVIAISYFITSLSYANS
CLNPFLYAFLDASFRRNLRQLITCRAAA
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  Blast E-value cutoff:
BDBM75925
n/a
NameBDBM75925
Synonyms:5-chloranyl-2-(4-propan-2-ylphenyl)-4-[4-(trifluoromethyloxy)phenoxy]pyridazin-3-one | 5-chloro-2-(4-propan-2-ylphenyl)-4-[4-(trifluoromethoxy)phenoxy]-3-pyridazinone | 5-chloro-2-(4-propan-2-ylphenyl)-4-[4-(trifluoromethoxy)phenoxy]pyridazin-3-one | 5-chloro-2-p-cumenyl-4-[4-(trifluoromethoxy)phenoxy]pyridazin-3-one | SR-02000000458 | SR-02000000458-1 | cid_46835812
TypeSmall organic molecule
Emp. Form.C20H16ClF3N2O3
Mol. Mass.424.801
SMILESCC(C)c1ccc(cc1)-n1ncc(Cl)c(Oc2ccc(OC(F)(F)F)cc2)c1=O
Structure
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