BDBM12078 6-Chloro-4-cyclohexyloxy-3-propyl-1H-quinol-2-one::6-chloro-4-(cyclohexyloxy)-3-propyl-1,2-dihydroquinolin-2-one::quinolone-based inhibitor 2a

SMILES: CCCc1c(OC2CCCCC2)c2cc(Cl)ccc2[nH]c1=O

InChI Key: InChIKey=BNZHKKGOSYAQSW-UHFFFAOYSA-N

Data: 3 IC50

PDB links: 1 PDB ID matches this monomer.

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 3 hits for monomerid = 12078   

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
HIV-1 Reverse Transcriptase (Human immunodeficiency virus type 1)	BDBM12078 (6-Chloro-4-cyclohexyloxy-3-propyl-1H-quinol-2-one ...) Show SMILES CCCc1c(OC2CCCCC2)c2cc(Cl)ccc2[nH]c1=O Show InChI InChI=1S/C18H22ClNO2/c1-2-6-14-17(22-13-7-4-3-5-8-13)15-11-12(19)9-10-16(15)20-18(14)21/h9-11,13H,2-8H2,1H3,(H,20,21)	PDB MMDB B.MOAD GoogleScholar AffyNet	Purchase DrugBank MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	n/a	n/a	710	n/a	n/a	n/a	n/a	7.8	22
University of Oxford					Assay Description The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.				J Med Chem 47: 5912-22 (2004) Article DOI: 10.1021/jm040071z BindingDB Entry DOI: 10.7270/Q2ZG6QGC
					More data for this Ligand-Target Pair				3D Structure (crystal)
HIV-1 Reverse Transcriptase Mutant (L100I) (Human immunodeficiency virus type 1)	BDBM12078 (6-Chloro-4-cyclohexyloxy-3-propyl-1H-quinol-2-one ...) Show SMILES CCCc1c(OC2CCCCC2)c2cc(Cl)ccc2[nH]c1=O Show InChI InChI=1S/C18H22ClNO2/c1-2-6-14-17(22-13-7-4-3-5-8-13)15-11-12(19)9-10-16(15)20-18(14)21/h9-11,13H,2-8H2,1H3,(H,20,21)	PDB MMDB B.MOAD GoogleScholar AffyNet	Purchase DrugBank MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	n/a	n/a	1.36E+3	n/a	n/a	n/a	n/a	7.8	22
University of Oxford					Assay Description The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.				J Med Chem 47: 5912-22 (2004) Article DOI: 10.1021/jm040071z BindingDB Entry DOI: 10.7270/Q2ZG6QGC
					More data for this Ligand-Target Pair				3D Structure (crystal)
HIV-1 Reverse Transcriptase Mutant (Y181C) (Human immunodeficiency virus type 1)	BDBM12078 (6-Chloro-4-cyclohexyloxy-3-propyl-1H-quinol-2-one ...) Show SMILES CCCc1c(OC2CCCCC2)c2cc(Cl)ccc2[nH]c1=O Show InChI InChI=1S/C18H22ClNO2/c1-2-6-14-17(22-13-7-4-3-5-8-13)15-11-12(19)9-10-16(15)20-18(14)21/h9-11,13H,2-8H2,1H3,(H,20,21)	PDB MMDB B.MOAD GoogleScholar AffyNet	Purchase DrugBank MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	n/a	n/a	1.13E+3	n/a	n/a	n/a	n/a	7.8	22
University of Oxford					Assay Description The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.				J Med Chem 47: 5912-22 (2004) Article DOI: 10.1021/jm040071z BindingDB Entry DOI: 10.7270/Q2ZG6QGC
					More data for this Ligand-Target Pair				3D Structure (crystal)