BDBM14088 (2S)-N-[(2S)-2-(1,3-benzothiazol-2-ylcarbonyl)-5-carbamimidamidopentan-2-yl]-1-[(2R)-2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide::2-ketobenzothiazole 28

SMILES [#6]-[#7]-[#6@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7][C@@]([#6])([#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])[#6](=O)-c1nc2ccccc2s1

InChI Key InChIKey=QIVIRMCXSHIRPU-BXOOBUKZSA-N

Data  2 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 14088   

TargetProthrombin(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM14088((2S)-N-[(2S)-2-(1,3-benzothiazol-2-ylcarbonyl)-5-c...)
Affinity DataKi:  430nM IC50:  3.70E+3nMAssay Description:Thrombin-catalyzed hydrolysis rates were measured spectrophotometrically using human alpha-thrombin, a chromogenic substrate in aqueous buffer, and a...More data for this Ligand-Target Pair
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TargetSerine protease 1(Bos taurus (bovine))
Johnson & Johnson Pharmaceutical

LigandPNGBDBM14088((2S)-N-[(2S)-2-(1,3-benzothiazol-2-ylcarbonyl)-5-c...)
Affinity DataKi:  6.00E+3nMAssay Description:Trypsin-catalyzed hydrolysis rates were measured spectrophotometrically using bovine trypsin, a chromogenic substrate in aqueous buffer, and a microp...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed