BDBM50002665 (10R,11S)-6,6,10,11-Tetramethyl-4-propyl-10,11-dihydro-6H-dipyrano[2,3-f;2',3'-h]chromene-2,12-dione::6,6,10,11-Tetramethyl-4-propyl-10,11-dihydro-6H-dipyrano[2,3-f;2',3'-h]chromene-2,12-dione::CHEMBL7378

SMILES: CCCc1cc(=O)oc2c3C(=O)[C@@H](C)[C@@H](C)Oc3c3C=CC(C)(C)Oc3c12

InChI Key: InChIKey=HQVBDUZROQMWRN-NWDGAFQWSA-N

Data: 1 EC50

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 = 50002665   

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
Human immunodeficiency virus type 1 reverse transcriptase (Human immunodeficiency virus 1)	BDBM50002665 ((10R,11S)-6,6,10,11-Tetramethyl-4-propyl-10,11-dih...) Show SMILES CCCc1cc(=O)oc2c3C(=O)[C@@H](C)[C@@H](C)Oc3c3C=CC(C)(C)Oc3c12 |c:20| Show InChI InChI=1S/C22H24O5/c1-6-7-13-10-15(23)26-21-16(13)20-14(8-9-22(4,5)27-20)19-17(21)18(24)11(2)12(3)25-19/h8-12H,6-7H2,1-5H3/t11-,12+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a
MediChem Research, Inc. Curated by ChEMBL					Assay Description Inhibition of HIV-1 reverse transcriptase using a poly(rC):oligo(dG)12-18 template primer				J Med Chem 40: 1005-17 (1997) Article DOI: 10.1021/jm960355m BindingDB Entry DOI: 10.7270/Q2N015NG
					More data for this Ligand-Target Pair