BDBM50214282 CHEMBL3350413

SMILES: CSCOC1(C)COC(C)(CC(=O)OC[C@H]2O[C@H](C(O)=C2)n2cnc3c(N)ncnc23)C1

InChI Key: InChIKey=DNDWDWQZSPXDGJ-FTPXCDOSSA-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 = 50214282   

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
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50214282 (CHEMBL3350413) Show SMILES CSCOC1(C)COC(C)(CC(=O)OC[C@H]2O[C@H](C(O)=C2)n2cnc3c(N)ncnc23)C1 |r,c:19| Show InChI InChI=1S/C20H27N5O6S/c1-19(7-20(2,8-29-19)30-11-32-3)5-14(27)28-6-12-4-13(26)18(31-12)25-10-24-15-16(21)22-9-23-17(15)25/h4,9-10,12,18,26H,5-8,11H2,1-3H3,(H2,21,22,23)/t12-,18+,19?,20?/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of HIV-1 reverse transcriptase				Bioorg Med Chem Lett 6: 2411-2416 (1996) Article DOI: 10.1016/0960-894X(96)00443-X BindingDB Entry DOI: 10.7270/Q2TB16VK
					More data for this Ligand-Target Pair