BDBM50304292 2-((2S,3S,5R)-2-(hydroxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-ylamino)-2-oxoacetic acid::CHEMBL593706

SMILES: Cc1cn([C@H]2C[C@H](NC(=O)C(O)=O)[C@@H](CO)O2)c(=O)[nH]c1=O

InChI Key: InChIKey=NUOQPEKNHWXSKJ-XLPZGREQSA-N

Data: 1 KI

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 = 50304292   

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
RNAse A (Homo sapiens (Human))	BDBM50304292 (2-((2S,3S,5R)-2-(hydroxymethyl)-5-(5-methyl-2,4-di...) Show SMILES Cc1cn([C@H]2C[C@H](NC(=O)C(O)=O)[C@@H](CO)O2)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C12H15N3O7/c1-5-3-15(12(21)14-9(5)17)8-2-6(7(4-16)22-8)13-10(18)11(19)20/h3,6-8,16H,2,4H2,1H3,(H,13,18)(H,19,20)(H,14,17,21)/t6-,7+,8+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.32E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Technology Curated by ChEMBL					Assay Description Inhibition of RNase A using dixon plot by spectrophotometric method				Bioorg Med Chem 17: 6491-5 (2009) Article DOI: 10.1016/j.bmc.2009.08.018 BindingDB Entry DOI: 10.7270/Q2XG9R61
					More data for this Ligand-Target Pair