Reaction Details |
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Target | Vasopressin V1b receptor |
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Ligand | BDBM175212 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Binding Assay |
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pH | 7.4±n/a |
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Temperature | 298.15±n/a K |
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Ki | <1.00±n/a nM |
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Comments | extracted |
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Citation | Geneste, H; Hornberger, W; Jantos, K; Kling, A; Van Gaalen, M Oxindole compounds carrying a nitrogen-bound spiro substituent and use thereof for treating vasopressin-related diseases US Patent US9688678 Publication Date 6/27/2017 |
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More Info.: | Get all data from this article, Assay Method |
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Vasopressin V1b receptor |
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Name: | Vasopressin V1b receptor |
Synonyms: | AVPR V1b | AVPR V3 | AVPR1B | AVPR3 | Antidiuretic hormone receptor 1b | V1BR_HUMAN | V1bR | VASOPRESSIN V1B | VPR3 | Vasopressin V1b receptor | Vasopressin V1b receptor (V1b) | Vasopressin V3 | Vasopressin V3 receptor |
Type: | Enzyme |
Mol. Mass.: | 46985.01 |
Organism: | Homo sapiens (Human) |
Description: | P47901 |
Residue: | 424 |
Sequence: | MDSGPLWDANPTPRGTLSAPNATTPWLGRDEELAKVEIGVLATVLVLATGGNLAVLLTLG
QLGRKRSRMHLFVLHLALTDLAVALFQVLPQLLWDITYRFQGPDLLCRAVKYLQVLSMFA
STYMLLAMTLDRYLAVCHPLRSLQQPGQSTYLLIAAPWLLAAIFSLPQVFIFSLREVIQG
SGVLDCWADFGFPWGPRAYLTWTTLAIFVLPVTMLTACYSLICHEICKNLKVKTQAWRVG
GGGWRTWDRPSPSTLAATTRGLPSRVSSINTISRAKIRTVKMTFVIVLAYIACWAPFFSV
QMWSVWDKNAPDEDSTNVAFTISMLLGNLNSCCNPWIYMGFNSHLLPRPLRHLACCGGPQ
PRMRRRLSDGSLSSRHTTLLTRSSCPATLSLSLSLTLSGRPRPEESPRDLELADGEGTAE
TIIF
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BDBM175212 |
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n/a |
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Name | BDBM175212 |
Synonyms: | US9688678, 34 (3S)-1-[(5-chloro-2-pyridyl)sulfonyl]-3-(2-ethoxy-5-methoxy-phenyl)-3-[2-(1-methyl-4-piperidyl)-2,6-diazaspiro[3.3]heptan-6-yl]-2-oxo-indoline-5-carbonitrile |
Type | Small organic molecule |
Emp. Form. | C34H39ClN6O5S |
Mol. Mass. | 679.229 |
SMILES | CCOc1ccc(OC)cc1[C@]1(C2C=C(C=CC2N(C1=O)S(=O)(=O)c1ccc(Cl)cn1)C#N)N1CC2(CN(C2)C2CCN(C)CC2)C1 |r,c:14,16| |
Structure |
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