null

SMILES: Cc1c(Sc2ccccc2)n(COCCOP(O)(=O)P(O)(=O)P(O)(O)=O)c(=O)[nH]c1=O

InChI Key: InChIKey=PSIUQLQXSUBKJL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50016535   

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)	BDBM50016535 (5-methyl-6-(phenylthio)-1-({2-[(1,2,3,3-tetrahydro...) Show SMILES Cc1c(Sc2ccccc2)n(COCCOP(O)(=O)P(O)(=O)P(O)(O)=O)c(=O)[nH]c1=O Show InChI InChI=1S/C14H19N2O11P3S/c1-10-12(17)15-14(18)16(13(10)31-11-5-3-2-4-6-11)9-26-7-8-27-29(22,23)30(24,25)28(19,20)21/h2-6H,7-9H2,1H3,(H,22,23)(H,24,25)(H,15,17,18)(H2,19,20,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Showa University Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 reverse transcriptase activity using poly(rC)-oligo(dG) template primer				J Med Chem 32: 2507-9 (1989) BindingDB Entry DOI: 10.7270/Q2HH6J27
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50016535 (5-methyl-6-(phenylthio)-1-({2-[(1,2,3,3-tetrahydro...) Show SMILES Cc1c(Sc2ccccc2)n(COCCOP(O)(=O)P(O)(=O)P(O)(O)=O)c(=O)[nH]c1=O Show InChI InChI=1S/C14H19N2O11P3S/c1-10-12(17)15-14(18)16(13(10)31-11-5-3-2-4-6-11)9-26-7-8-27-29(22,23)30(24,25)28(19,20)21/h2-6H,7-9H2,1H3,(H,22,23)(H,24,25)(H,15,17,18)(H2,19,20,21)	PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Showa University Curated by ChEMBL					Assay Description Inhibitory effect of the compound on HIV-1 reverse transcriptase activity using poly(rA)-oligo(dT) template primer				J Med Chem 32: 2507-9 (1989) BindingDB Entry DOI: 10.7270/Q2HH6J27
					More data for this Ligand-Target Pair