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TargetTryptase beta-2
LigandBDBM50103791
Substrate/Competitorn/a
Meas. Tech.ChEBML_210702
Ki 50000±n/a nM
Citation Dener, JMWang, VRRice, KDGangloff, ARKuo, EYNewcomb, WSPutnam, DWong, M Monocharged inhibitors of mast cell tryptase derived from potent and selective dibasic inhibitors. Bioorg Med Chem Lett11:2325-30 (2001) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Tryptase beta-2
Name:Tryptase beta-2
Synonyms:TPS2 | TPSB2 | TRYB2_HUMAN | Tryptase | Tryptase II | Tryptase beta-1 | Tryptase-2
Type:PROTEIN
Mol. Mass.:30518.79
Organism:Homo sapiens (Human)
Description:ChEMBL_210702
Residue:275
Sequence:
MLNLLLLALPVLASRAYAAPAPGQALQRVGIVGGQEAPRSKWPWQVSLRVHGPYWMHFCG
GSLIHPQWVLTAAHCVGPDVKDLAALRVQLREQHLYYQDQLLPVSRIIVHPQFYTAQIGA
DIALLELEEPVNVSSHVHTVTLPPASETFPPGMPCWVTGWGDVDNDERLPPPFPLKQVKV
PIMENHICDAKYHLGAYTGDDVRIVRDDMLCAGNTRRDSCQGDSGGPLVCKVNGTWLQAG
VVSWGEGCAQPNRPGIYTRVTYYLDWIHHYVPKKP
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  Blast E-value cutoff:
BDBM50103791
n/a
NameBDBM50103791
Synonyms:4-{[(4-Carbamimidoyl-benzoyl)-methyl-amino]-methyl}-piperidine-1-carboxylic acid (3,3-diphenyl-propyl)-amide | CHEMBL308376
TypeSmall organic molecule
Emp. Form.C31H37N5O2
Mol. Mass.511.6578
SMILESCN(CC1CCN(CC1)C(=O)NCCC(c1ccccc1)c1ccccc1)C(=O)c1ccc(cc1)C(N)=N
Structure
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