Reaction Details |
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Target | Vasopressin V1a receptor |
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Ligand | BDBM50087545 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_214551 |
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IC50 | 2100±n/a nM |
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Citation | Albright, JD; Delos Santos, EG; Dusza, JP; Chan, PS; Coupet, J; Ru, X; Mazandarani, H The synthesis and vasopressin (AVP) antagonist activity of a novel series of N-aroyl-2,4,5,6-tetrahydropyrazolo[3,4-d]thieno[3,2-b]azepines. Bioorg Med Chem Lett10:695-8 (2000) [PubMed] |
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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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BDBM50087545 |
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n/a |
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Name | BDBM50087545 |
Synonyms: | 2,4-Dichloro-N-[4-(2-methyl-4,5-dihydro-2H-9-thia-1,2,6-triaza-cyclopenta[e]azulene-6-carbonyl)-phenyl]-benzamide | CHEMBL349506 |
Type | Small organic molecule |
Emp. Form. | C24H18Cl2N4O2S |
Mol. Mass. | 497.396 |
SMILES | Cn1cc2CCN(C(=O)c3ccc(NC(=O)c4ccc(Cl)cc4Cl)cc3)c3ccsc3-c2n1 |
Structure |
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