BDBM403661 (4aR,8S,11S,12S,13R,25aR)-8-tert-butyl-N-[(1R,2R)-1-[(cyclopropylsulfonyl)carbamoyl]-2-(difluoromethyl)cyclopropyl]-17-methoxy-12-methyl-6,9-dioxo-2,3,4,4a,6,7,8,9,12,13,21,22,23,24,25,25a-hexadecahydro-1H,11H-1,3,10,13-dimethanoquinoxalino[2,3-k][1,10,3,6]benzodioxadiazacyclononadecine-11-carboxamide and::US10335409, Example 71

SMILES: COc1ccc2nc3CCCCC[C@H]4C5CC(C5)C[C@@H]4OC(=O)N[C@H](C(=O)N4C[C@H](Oc3nc2c1)[C@@H](C)[C@H]4C(O)=O)C(C)(C)C

InChI Key: InChIKey=ZMNVOUOJNPWSTB-HQEUCTODSA-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 = 403661   

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))	BDBM403661 ((4aR,8S,11S,12S,13R,25aR)-8-tert-butyl-N-[(1R,2R)-...) Show SMILES COc1ccc2nc3CCCCC[C@H]4C5CC(C5)C[C@@H]4OC(=O)N[C@H](C(=O)N4C[C@H](Oc3nc2c1)[C@@H](C)[C@H]4C(O)=O)C(C)(C)C |r,wU:35.40,37.43,19.19,wD:29.30,24.46,13.12,(5.02,-14.55,;3.68,-13.78,;2.35,-14.55,;1.02,-13.78,;-.32,-14.55,;-.32,-16.09,;-1.65,-16.86,;-1.65,-18.4,;-3.98,-19.71,;-3.98,-21.25,;-5.31,-22.02,;-5.31,-23.56,;-6.64,-24.33,;-6.64,-25.87,;-7.98,-26.64,;-7.98,-28.18,;-6.64,-28.95,;-6.64,-27.41,;-5.31,-28.18,;-5.31,-26.64,;-3.98,-25.87,;-2.64,-26.64,;-2.64,-28.18,;-1.31,-25.87,;.02,-26.64,;1.36,-25.87,;2.69,-26.64,;1.36,-24.33,;.11,-23.42,;.59,-21.96,;-.32,-20.71,;-.32,-19.17,;1.02,-18.4,;1.02,-16.86,;2.35,-16.09,;2.13,-21.96,;3.03,-20.71,;2.6,-23.42,;3.94,-24.19,;5.27,-23.42,;3.94,-25.73,;.02,-28.18,;1.36,-28.95,;-1.31,-28.95,;.02,-29.72,)| Show InChI InChI=1S/C34H46N4O7/c1-18-27-17-38(28(18)32(40)41)31(39)29(34(2,3)4)37-33(42)45-26-15-19-13-20(14-19)22(26)9-7-6-8-10-24-30(44-27)36-25-16-21(43-5)11-12-23(25)35-24/h11-12,16,18-20,22,26-29H,6-10,13-15,17H2,1-5H3,(H,37,42)(H,40,41)/t18-,19?,20?,22+,26+,27+,28+,29-/m1/s1	PDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.0300	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))	BDBM403661 ((4aR,8S,11S,12S,13R,25aR)-8-tert-butyl-N-[(1R,2R)-...) Show SMILES COc1ccc2nc3CCCCC[C@H]4C5CC(C5)C[C@@H]4OC(=O)N[C@H](C(=O)N4C[C@H](Oc3nc2c1)[C@@H](C)[C@H]4C(O)=O)C(C)(C)C |r,wU:35.40,37.43,19.19,wD:29.30,24.46,13.12,(5.02,-14.55,;3.68,-13.78,;2.35,-14.55,;1.02,-13.78,;-.32,-14.55,;-.32,-16.09,;-1.65,-16.86,;-1.65,-18.4,;-3.98,-19.71,;-3.98,-21.25,;-5.31,-22.02,;-5.31,-23.56,;-6.64,-24.33,;-6.64,-25.87,;-7.98,-26.64,;-7.98,-28.18,;-6.64,-28.95,;-6.64,-27.41,;-5.31,-28.18,;-5.31,-26.64,;-3.98,-25.87,;-2.64,-26.64,;-2.64,-28.18,;-1.31,-25.87,;.02,-26.64,;1.36,-25.87,;2.69,-26.64,;1.36,-24.33,;.11,-23.42,;.59,-21.96,;-.32,-20.71,;-.32,-19.17,;1.02,-18.4,;1.02,-16.86,;2.35,-16.09,;2.13,-21.96,;3.03,-20.71,;2.6,-23.42,;3.94,-24.19,;5.27,-23.42,;3.94,-25.73,;.02,-28.18,;1.36,-28.95,;-1.31,-28.95,;.02,-29.72,)| Show InChI InChI=1S/C34H46N4O7/c1-18-27-17-38(28(18)32(40)41)31(39)29(34(2,3)4)37-33(42)45-26-15-19-13-20(14-19)22(26)9-7-6-8-10-24-30(44-27)36-25-16-21(43-5)11-12-23(25)35-24/h11-12,16,18-20,22,26-29H,6-10,13-15,17H2,1-5H3,(H,37,42)(H,40,41)/t18-,19?,20?,22+,26+,27+,28+,29-/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.140	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