Reaction Details |
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Target | Vasopressin V1a receptor |
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Ligand | BDBM50285296 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_214549 (CHEMBL820018) |
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IC50 | 4140±n/a nM |
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Citation | Hobbs, DW; Gould, NP; Hoffman, JB; Clineschmidt, BV; Pettibone, DJ; Veber, DF; Freidinger, RM Non-peptide oxytocin antagonists: identification and synthesis of a potent camphor aminosuccinimide Bioorg Med Chem Lett5:119-122 (1995) Article |
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More Info.: | Get all data from this article, Assay Method |
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Vasopressin V1a receptor |
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Name: | Vasopressin V1a receptor |
Synonyms: | Avpr1a | V1AR_RAT | VASOPRESSIN V1A | Vasopressin V1 receptor | Vasopressin V1a receptor | Vasopressin receptor |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 47674.81 |
Organism: | RAT |
Description: | VASOPRESSIN V1A AVPR1A RAT::P30560 |
Residue: | 424 |
Sequence: | MSFPRGSQDRSVGNSSPWWPLTTEGSNGSQEAARLGEGDSPLGDVRNEELAKLEIAVLAV
IFVVAVLGNSSVLLALHRTPRKTSRMHLFIRHLSLADLAVAFFQVLPQLCWDITYRFRGP
DWLCRVVKHLQVFAMFASAYMLVVMTADRYIAVCHPLKTLQQPARRSRLMIATSWVLSFI
LSTPQYFIFSVIEIEVNNGTKTQDCWATFIQPWGTRAYVTWMTSGVFVAPVVVLGTCYGF
ICYHIWRNIRGKTASSRHSKGDKGSGEAVGPFHKGLLVTPCVSSVKSISRAKIRTVKMTF
VIVSAYILCWAPFFIVQMWSVWDENFIWTDSENPSITITALLASLNSCCNPWIYMFFSGH
LLQDCVQSFPCCHSMAQKFAKDDSDSMSRRQTSYSNNRSPTNSTGMWKDSPKSSKSIRFI
PVST
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BDBM50285296 |
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n/a |
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Name | BDBM50285296 |
Synonyms: | 1-[7,7-dimethyl-1-spiro[2,3-dihydro-1H-indene-1,4'-(hexahydropyridine)]-1-ylsulfonylmethyl-(1S,2S)-bicyclo[2.2.1]hept-2-yl]-2,5-dihydro-1H-2,5-pyrroledione | CHEMBL20205 |
Type | Small organic molecule |
Emp. Form. | C27H34N2O4S |
Mol. Mass. | 482.635 |
SMILES | CC1(C)C2CC[C@@]1(CS(=O)(=O)N1CCC3(CCc4ccccc34)CC1)[C@H](C2)N1C(=O)C=CC1=O |c:35| |
Structure |
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