BDBM403597 Preparation of (1aR,5S,8S,9S,10R,22aR)-5-tert-butyl-N-[(1R,2R)-2-(difluoromethyl)-1-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}cyclopropyl]-9-ethyl-14-methoxy-1a-methyl-3,6-dioxo-1,1a,3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocyclopropa[18,19][1,10,3,6] dioxadiazacyclononadecino[11,12-b]quinoxaline-8-carboxamide::US10335409, Example 7

SMILES: CC[C@@H]1[C@H](CN([C@@H]1C(=O)OC(C)(C)C)C(=O)[C@@H](NC(=O)OC1(C)CC1CCCC=C)C(C)(C)C)Oc1nc2cc(OC)ccc2nc1Cl

InChI Key: InChIKey=IUQRUQJXIQWRQF-KYBDLAEPSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 403597   

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
NS3 serine protease (NS3) (Hepatitis C Virus (Virus))	BDBM403597 (Preparation of (1aR,5S,8S,9S,10R,22aR)-5-tert-buty...) Show SMILES CC[C@@H]1[C@H](CN([C@@H]1C(=O)OC(C)(C)C)C(=O)[C@@H](NC(=O)OC1(C)CC1CCCC=C)C(C)(C)C)Oc1nc2cc(OC)ccc2nc1Cl |r| Show InChI InChI=1S/C36H51ClN4O7/c1-11-13-14-15-21-19-36(21,9)48-33(44)40-28(34(3,4)5)31(42)41-20-26(23(12-2)27(41)32(43)47-35(6,7)8)46-30-29(37)38-24-17-16-22(45-10)18-25(24)39-30/h11,16-18,21,23,26-28H,1,12-15,19-20H2,2-10H3,(H,40,44)/t21?,23-,26+,27+,28-,36?/m1/s1	PDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.0500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
SRMLSC Curated by PubChem BioAssay					Assay Description Purified NS3 protease domain (amino acids 1-181) of the genotype 1b and 3a virus were generated as above. The internally quenched fluorogenic depsipe...				PubChem Bioassay (2006) BindingDB Entry DOI: 10.7270/Q2930WJC
					More data for this Ligand-Target Pair
Genome polyprotein (Hepatitis C virus genotype 3a (isolate k3a) (HCV))	BDBM403597 (Preparation of (1aR,5S,8S,9S,10R,22aR)-5-tert-buty...) Show SMILES CC[C@@H]1[C@H](CN([C@@H]1C(=O)OC(C)(C)C)C(=O)[C@@H](NC(=O)OC1(C)CC1CCCC=C)C(C)(C)C)Oc1nc2cc(OC)ccc2nc1Cl |r| Show InChI InChI=1S/C36H51ClN4O7/c1-11-13-14-15-21-19-36(21,9)48-33(44)40-28(34(3,4)5)31(42)41-20-26(23(12-2)27(41)32(43)47-35(6,7)8)46-30-29(37)38-24-17-16-22(45-10)18-25(24)39-30/h11,16-18,21,23,26-28H,1,12-15,19-20H2,2-10H3,(H,40,44)/t21?,23-,26+,27+,28-,36?/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.0600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
SRMLSC Curated by PubChem BioAssay					Assay Description Purified NS3 protease domain (amino acids 1-181) of the genotype 1b and 3a virus were generated as above. The internally quenched fluorogenic depsipe...				PubChem Bioassay (2006) BindingDB Entry DOI: 10.7270/Q2930WJC
					More data for this Ligand-Target Pair