Reaction Details |
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Target | Neuropeptides B/W receptor type 1 |
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Ligand | BDBM75900 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7) |
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IC50 | 280±n/a nM |
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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] |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Neuropeptides B/W receptor type 1 |
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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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BDBM75900 |
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n/a |
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Name | BDBM75900 |
Synonyms: | 5-chloranyl-4-(4-methoxyphenoxy)-2-(3-propan-2-ylphenyl)pyridazin-3-one | 5-chloro-2-m-cumenyl-4-(4-methoxyphenoxy)pyridazin-3-one | 5-chloro-4-(4-methoxyphenoxy)-2-(3-propan-2-ylphenyl)-3-pyridazinone | 5-chloro-4-(4-methoxyphenoxy)-2-(3-propan-2-ylphenyl)pyridazin-3-one | SR-02000000371 | SR-02000000371-1 | cid_46172924 |
Type | Small organic molecule |
Emp. Form. | C20H19ClN2O3 |
Mol. Mass. | 370.829 |
SMILES | COc1ccc(Oc2c(Cl)cnn(-c3cccc(c3)C(C)C)c2=O)cc1 |
Structure |
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