Reaction Details |
| Report a problem with these data |
Target | B1 bradykinin receptor |
---|
Ligand | BDBM50209744 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_434373 (CHEMBL919421) |
---|
Ki | 127±n/a nM |
---|
Citation | Biswas, K; Li, A; Chen, JJ; D'Amico, DC; Fotsch, C; Han, N; Human, J; Liu, Q; Norman, MH; Riahi, B; Yuan, C; Suzuki, H; Mareska, DA; Zhan, J; Clarke, DE; Toro, A; Groneberg, RD; Burgess, LE; Lester-Zeiner, D; Biddlecome, G; Manning, BH; Arik, L; Dong, H; Huang, M; Kamassah, A; Loeloff, R; Sun, H; Hsieh, FY; Kumar, G; Ng, GY; Hungate, RW; Askew, BC; Johnson, E Potent nonpeptide antagonists of the bradykinin B1 receptor: structure-activity relationship studies with novel diaminochroman carboxamides. J Med Chem50:2200-12 (2007) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
B1 bradykinin receptor |
---|
Name: | B1 bradykinin receptor |
Synonyms: | B1 BRADYKININ | B1R | B1bkr | BK-1 receptor | BKRB1_RAT | Bdkrb1 | Bkr | Bradykinin B1 receptor | KB1 | Kinin B1 receptor |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 38389.97 |
Organism: | RAT |
Description: | B1 BRADYKININ BDKRB1 RAT::P97583 |
Residue: | 337 |
Sequence: | MASEVLLELQPSNRSLQAPANITSCESALEDWDLLYRVLPGFVITICFFGLLGNLLVLSF
FLLPWRQWWWQQRQRQQRLTIAEIYLANLAASDLVFVLGLPFWAENIGNRFNWPFGTDLC
RVVSGVIKANLFVSIFLVVAISQDRYRLLVYPMTSWGYRRRRQAQATCLLIWVAGGLLSI
PTFLLRSVKVVPDLNVSACILLFPHEAWHFARMVELNVLGFLLPVTAIIFFNYHILASLR
GQKEASRTRCGGPKGSKTTGLILTLVASFLVCWCPYHFFAFLDFLVQVRVIQDCSWKEIT
DLGLQLANFFAFVNSCLNPLIYVFAGRLLKTRVLGTL
|
|
|
BDBM50209744 |
---|
n/a |
---|
Name | BDBM50209744 |
Synonyms: | (R)-3-(4-fluorophenyl)-N-((R)-7-(piperidin-1-ylmethyl)-3,4-dihydro-2H-chromen-4-yl)-3-(3-(trifluoromethyl)phenylsulfonamido)propanamide | (R)-3-(4-fluorophenyl)-N-((R)-7-(piperidin-1-ylmethyl)chroman-4-yl)-3-(3-(trifluoromethyl)phenylsulfonamido)-propanamide | CHEMBL227713 |
Type | Small organic molecule |
Emp. Form. | C31H33F4N3O4S |
Mol. Mass. | 619.67 |
SMILES | Fc1ccc(cc1)[C@@H](CC(=O)N[C@@H]1CCOc2cc(CN3CCCCC3)ccc12)NS(=O)(=O)c1cccc(c1)C(F)(F)F |r| |
Structure |
|