BDBM2060 2,8-disubstituted dipyridodiazepinone 43::2-Chloro-5,11-dihydro-11-ethyl-5-methyl-8-(1H-pyrazolo-[3,4-d]pyrimidin-4-ylthio)methyl-6H-dipyrido[3,2-b:2 ,3 -e][1,4]diazepin-6-one::5-chloro-2-ethyl-9-methyl-13-({1H-pyrazolo[3,4-d]pyrimidin-4-ylsulfanyl}methyl)-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

SMILES: CCN1c2ncc(CSc3ncnc4n[nH]cc34)cc2C(=O)N(C)c2ccc(Cl)nc12

InChI Key: InChIKey=HHTVAFPSLHBBQG-UHFFFAOYSA-N

Data: 3 IC50

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 = 2060   

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 Mutant (Y181C) (Human immunodeficiency virus type 1)	BDBM2060 (2,8-disubstituted dipyridodiazepinone 43 | 2-Chlor...) Show SMILES CCN1c2ncc(CSc3ncnc4n[nH]cc34)cc2C(=O)N(C)c2ccc(Cl)nc12 Show InChI InChI=1S/C20H17ClN8OS/c1-3-29-17-12(20(30)28(2)14-4-5-15(21)26-18(14)29)6-11(7-22-17)9-31-19-13-8-25-27-16(13)23-10-24-19/h4-8,10H,3,9H2,1-2H3,(H,23,24,25,27)	PDB MMDB B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharmaceuticals Inc.					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 41: 2972-84 (1998) Article DOI: 10.1021/jm9707030 BindingDB Entry DOI: 10.7270/Q2J964K7
					More data for this Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase (Human immunodeficiency virus 1)	BDBM2060 (2,8-disubstituted dipyridodiazepinone 43 | 2-Chlor...) Show SMILES CCN1c2ncc(CSc3ncnc4n[nH]cc34)cc2C(=O)N(C)c2ccc(Cl)nc12 Show InChI InChI=1S/C20H17ClN8OS/c1-3-29-17-12(20(30)28(2)14-4-5-15(21)26-18(14)29)6-11(7-22-17)9-31-19-13-8-25-27-16(13)23-10-24-19/h4-8,10H,3,9H2,1-2H3,(H,23,24,25,27)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharmaceuticals Inc.					Assay Description Inhibitory activity against HIV-1 Y188L reverse transcriptase.				J Med Chem 41: 2972-84 (1998) Article DOI: 10.1021/jm9707030 BindingDB Entry DOI: 10.7270/Q2J964K7
					More data for this Ligand-Target Pair
HIV-1 Reverse Transcriptase Mutant (Y188L) (Human immunodeficiency virus type 1)	BDBM2060 (2,8-disubstituted dipyridodiazepinone 43 | 2-Chlor...) Show SMILES CCN1c2ncc(CSc3ncnc4n[nH]cc34)cc2C(=O)N(C)c2ccc(Cl)nc12 Show InChI InChI=1S/C20H17ClN8OS/c1-3-29-17-12(20(30)28(2)14-4-5-15(21)26-18(14)29)6-11(7-22-17)9-31-19-13-8-25-27-16(13)23-10-24-19/h4-8,10H,3,9H2,1-2H3,(H,23,24,25,27)	PDB MMDB B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharmaceuticals Inc.					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 41: 2972-84 (1998) Article DOI: 10.1021/jm9707030 BindingDB Entry DOI: 10.7270/Q2J964K7
					More data for this Ligand-Target Pair