null

SMILES: NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O

InChI Key: InChIKey=NOEVYCIBQDTBMB-UHFFFAOYSA-O

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50085515   

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
Coagulation factor X (Homo sapiens (Human))	BDBM50085515 (Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...) Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	34	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Pharmaceuticals Company Curated by ChEMBL					Assay Description Inhibition of coagulation factor Xa				Bioorg Med Chem Lett 10: 301-4 (2000) BindingDB Entry DOI: 10.7270/Q2639Q7R
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50085515 (Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...) Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Pharmaceuticals Company Curated by ChEMBL					Assay Description Inhibitory activity against trypsin				Bioorg Med Chem Lett 10: 301-4 (2000) BindingDB Entry DOI: 10.7270/Q2639Q7R
					More data for this Ligand-Target Pair
Prothrombin (Homo sapiens (Human))	BDBM50085515 (Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...) Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	PubMed	2.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Pharmaceuticals Company Curated by ChEMBL					Assay Description Inhibitory activity against thrombin				Bioorg Med Chem Lett 10: 301-4 (2000) BindingDB Entry DOI: 10.7270/Q2639Q7R
					More data for this Ligand-Target Pair