BDBM50214280 CHEMBL3142412

SMILES: CC1=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C(=O)NC1

InChI Key: InChIKey=WITZMRTVNXDDGX-DJLDLDEBSA-N

Data: 2 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 2 hits for monomerid = 50214280   

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)	BDBM50214280 (CHEMBL3142412) Show SMILES CC1=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C(=O)NC1 |r,t:1| Show InChI InChI=1S/C10H16N2O4/c1-6-3-11-10(15)12(4-6)9-2-7(14)8(5-13)16-9/h4,7-9,13-14H,2-3,5H2,1H3,(H,11,15)/t7-,8+,9+/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: 2405-2410 (1996) Article DOI: 10.1016/0960-894X(96)00444-1 BindingDB Entry DOI: 10.7270/Q2Z31ZMC
					More data for this Ligand-Target Pair
Reverse transcriptase/RNaseH (Human immunodeficiency virus 1)	BDBM50214280 (CHEMBL3142412) Show SMILES CC1=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C(=O)NC1 |r,t:1| Show InChI InChI=1S/C10H16N2O4/c1-6-3-11-10(15)12(4-6)9-2-7(14)8(5-13)16-9/h4,7-9,13-14H,2-3,5H2,1H3,(H,11,15)/t7-,8+,9+/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