Target
Neuropeptides B/W receptor type 1
Ligand
BDBM75953
Substrate
n/a
Meas. Tech.
Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7)
IC50
>20000±n/a nM
Citation
 PubChem, PC Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7) PubChem Bioassay (2010)[AID] 
Target
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:
MDNASFSEPWPANASGPDPALSCSNASTLAPLPAPLAVAVPVVYAVICAVGLAGNSAVLYVLLRAPRMKTVTNLFILNLAIADELFTLVLPINIADFLLRQWPFGELMCKLIVAIDQYNTFSSLYFLTVMSADRYLVVLATAESRRVAGRTYSAARAVSLAVWGIVTLVVLPFAVFARLDDEQGRRQCVLVFPQPEAFWWRASRLYTLVLGFAIPVSTICVLYTTLLCRLHAMRLDSHAKALERAKKRVTFLVVAILAVCLLCWTPYHLSTVVALTTDLPQTPLVIAISYFITSLSYANSCLNPFLYAFLDASFRRNLRQLITCRAAA
  
Inhibitor
Name:
BDBM75953
Synonyms:
5-chloranyl-4-[2-(3,4-diethoxyphenyl)ethoxy]-2-phenyl-pyridazin-3-one | 5-chloro-4-[2-(3,4-diethoxyphenyl)ethoxy]-2-phenyl-3-pyridazinone | 5-chloro-4-[2-(3,4-diethoxyphenyl)ethoxy]-2-phenyl-pyridazin-3-one | 5-chloro-4-[2-(3,4-diethoxyphenyl)ethoxy]-2-phenylpyridazin-3-one | SR-02000000343 | SR-02000000343-1 | cid_45382321
Type:
Small organic molecule
Emp. Form.:
C22H23ClN2O4
Mol. Mass.:
414.882
SMILES:
CCOc1ccc(CCOc2c(Cl)cnn(-c3ccccc3)c2=O)cc1OCC
Structure:
Search PDB for entries with ligand similarity: