BDBM50046722 CHEMBL3310877

SMILES: [H][C@]12Sc3ncccc3C(=O)N1[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O

InChI Key: InChIKey=CUICHRZFNJIZLL-DXJNRASMSA-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 = 50046722   

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 (Human immunodeficiency virus 1)	BDBM50046722 (CHEMBL3310877) Show SMILES [H][C@]12Sc3ncccc3C(=O)N1[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O |r| Show InChI InChI=1S/C12H14N2O5S/c15-4-6-7(16)8(17)9(18)12-14(6)11(19)5-2-1-3-13-10(5)20-12/h1-3,6-9,12,15-18H,4H2/t6-,7-,8+,9+,12-/m1/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hebei University Curated by ChEMBL					Assay Description Inhibition of HIV-1 reverse transcriptase after 1 hr by ELISA plate reader analysis				Bioorg Med Chem Lett 24: 3426-9 (2014) Article DOI: 10.1016/j.bmcl.2014.05.079 BindingDB Entry DOI: 10.7270/Q25H7HWV
					More data for this Ligand-Target Pair