BDBM3386 7-[2-(1H-Imidazol-l-yl)-5-methylimidazo[1,5-b]pyridazin-7-yl]-1-phenyl-1-heptanone::7-[2-(1H-imidazol-1-yl)-5-methylimidazo[1,5-a]pyridazin-7-yl]-1-phenylheptan-1-one::Imidazopyridazine 33

SMILES: Cc1nc(CCCCCCC(=O)c2ccccc2)n2nc(ccc12)-n1ccnc1

InChI Key: InChIKey=IOUDUHWREIAEKP-UHFFFAOYSA-N

Data: 1 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 1 hit for monomerid = 3386   

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)	BDBM3386 (7-[2-(1H-Imidazol-l-yl)-5-methylimidazo[1,5-b]pyri...) Show SMILES Cc1nc(CCCCCCC(=O)c2ccccc2)n2nc(ccc12)-n1ccnc1 Show InChI InChI=1S/C23H25N5O/c1-18-20-13-14-23(27-16-15-24-17-27)26-28(20)22(25-18)12-8-3-2-7-11-21(29)19-9-5-4-6-10-19/h4-6,9-10,13-17H,2-3,7-8,11-12H2,1H3	PDB MMDB B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Group Research Ltd.					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 36: 3784-94 (1993) Article DOI: 10.1021/jm00076a005 BindingDB Entry DOI: 10.7270/Q2PR7T57
					More data for this Ligand-Target Pair