Reaction Details | |||
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Target | Vasopressin V1a receptor | ||
Ligand | BDBM50546433 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_2015644 (CHEMBL4669222) | ||
IC50 | 2.2±n/a nM | ||
Citation | Bozó, É; Baska, F; Lövei, K; Szántó, G; Domány-Kovács, K; Kurkó, D; Szondiné Kordás, K; Szokoli, T; Bata, I New V1a receptor antagonist. Part 2. Identification and optimization of triazolobenzazepines. Bioorg Med Chem Lett30:0 (2020) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Vasopressin V1a receptor | |||
Name: | Vasopressin V1a receptor | ||
Synonyms: | AVPR V1a | AVPR1 | AVPR1A | Antidiuretic hormone receptor 1a | V1AR_HUMAN | V1aR | VASOPRESSIN V1A | Vascular/hepatic-type arginine vasopressin receptor | Vasopressin V1 receptor | Vasopressin V1a receptor | Vasopressin receptor | ||
Type: | Receptor | ||
Mol. Mass.: | 46820.18 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P37288 | ||
Residue: | 418 | ||
Sequence: |
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BDBM50546433 | |||
n/a | |||
Name | BDBM50546433 | ||
Synonyms: | CHEMBL4756737 | ||
Type | Small organic molecule | ||
Emp. Form. | C21H23ClN4O | ||
Mol. Mass. | 382.887 | ||
SMILES | Cc1cc(no1)[C@H]1CC[C@@H](CC1)c1nnc2CCCc3cc(Cl)ccc3-n12 |r,wU:9.13,wD:6.6,(60.97,-1.63,;61.87,-2.87,;61.39,-4.32,;62.63,-5.22,;63.87,-4.33,;63.4,-2.87,;62.63,-6.75,;61.28,-7.51,;61.27,-9.05,;62.61,-9.84,;63.95,-9.07,;63.96,-7.52,;62.61,-11.38,;63.86,-12.28,;63.38,-13.74,;61.85,-13.74,;61.02,-15.04,;59.49,-15.2,;58.42,-14.1,;58.6,-12.57,;57.25,-11.84,;57.21,-10.3,;55.85,-9.57,;58.52,-9.49,;59.88,-10.23,;59.92,-11.76,;61.36,-12.28,)| | ||
Structure |