null

SMILES: CS(=O)(=O)N[C@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(cc1)C(N)=N

InChI Key: InChIKey=ZUYOUPIMWZZNEX-RBUKOAKNSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50111117   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prothrombin (Homo sapiens (Human))	BDBM50111117 ((S)-1-((R)-2-Cyclohexyl-2-methanesulfonylamino-ace...) Show SMILES CS(=O)(=O)N[C@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(cc1)C(N)=N Show InChI InChI=1S/C22H33N5O4S/c1-32(30,31)26-19(16-6-3-2-4-7-16)22(29)27-13-5-8-18(27)21(28)25-14-15-9-11-17(12-10-15)20(23)24/h9-12,16,18-19,26H,2-8,13-14H2,1H3,(H3,23,24)(H,25,28)/t18-,19+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Life Science R&D, LGCI Curated by ChEMBL					Assay Description Binding affinity against human thrombin				Bioorg Med Chem Lett 12: 1017-22 (2002) BindingDB Entry DOI: 10.7270/Q2CV4J9T
					More data for this Ligand-Target Pair
Serine protease 1 (Bos taurus (bovine))	BDBM50111117 ((S)-1-((R)-2-Cyclohexyl-2-methanesulfonylamino-ace...) Show SMILES CS(=O)(=O)N[C@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(cc1)C(N)=N Show InChI InChI=1S/C22H33N5O4S/c1-32(30,31)26-19(16-6-3-2-4-7-16)22(29)27-13-5-8-18(27)21(28)25-14-15-9-11-17(12-10-15)20(23)24/h9-12,16,18-19,26H,2-8,13-14H2,1H3,(H3,23,24)(H,25,28)/t18-,19+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Life Science R&D, LGCI Curated by ChEMBL					Assay Description Binding affinity against bovine trypsin				Bioorg Med Chem Lett 12: 1017-22 (2002) BindingDB Entry DOI: 10.7270/Q2CV4J9T
					More data for this Ligand-Target Pair
Coagulation factor X (Homo sapiens (Human))	BDBM50111117 ((S)-1-((R)-2-Cyclohexyl-2-methanesulfonylamino-ace...) Show SMILES CS(=O)(=O)N[C@H](C1CCCCC1)C(=O)N1CCC[C@H]1C(=O)NCc1ccc(cc1)C(N)=N Show InChI InChI=1S/C22H33N5O4S/c1-32(30,31)26-19(16-6-3-2-4-7-16)22(29)27-13-5-8-18(27)21(28)25-14-15-9-11-17(12-10-15)20(23)24/h9-12,16,18-19,26H,2-8,13-14H2,1H3,(H3,23,24)(H,25,28)/t18-,19+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Life Science R&D, LGCI Curated by ChEMBL					Assay Description Compound was evaluated for the binding affinity against human Coagulation factor Xa				Bioorg Med Chem Lett 12: 1017-22 (2002) BindingDB Entry DOI: 10.7270/Q2CV4J9T
					More data for this Ligand-Target Pair