null

SMILES: CC[C@@H]1N=C(N)[Se][C@@H]1C

InChI Key: InChIKey=TWHXDFKGBONPPR-UHNVWZDZSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50161390   

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
Nitric oxide synthase, inducible (Homo sapiens (Human))	BDBM50161390 ((4S,5R)-4-Ethyl-5-methyl-selenazolidin-(2Z)-yliden...) Show SMILES CC[C@@H]1N=C(N)[Se][C@@H]1C |t:3| Show InChI InChI=1S/C6H12N2Se/c1-3-5-4(2)9-6(7)8-5/h4-5H,3H2,1-2H3,(H2,7,8)/t4-,5+/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Dainippon Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description Inhibitory concentration against inducible nitric acid synthase				Bioorg Med Chem Lett 15: 1361-6 (2005) Article DOI: 10.1016/j.bmcl.2005.01.013 BindingDB Entry DOI: 10.7270/Q2G160B2
					More data for this Ligand-Target Pair
Nitric oxide synthase, brain (Homo sapiens (Human))	BDBM50161390 ((4S,5R)-4-Ethyl-5-methyl-selenazolidin-(2Z)-yliden...) Show SMILES CC[C@@H]1N=C(N)[Se][C@@H]1C |t:3| Show InChI InChI=1S/C6H12N2Se/c1-3-5-4(2)9-6(7)8-5/h4-5H,3H2,1-2H3,(H2,7,8)/t4-,5+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	740	n/a	n/a	n/a	n/a	n/a	n/a
Dainippon Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description Inhibitory concentration against neuronal nitric acid synthase				Bioorg Med Chem Lett 15: 1361-6 (2005) Article DOI: 10.1016/j.bmcl.2005.01.013 BindingDB Entry DOI: 10.7270/Q2G160B2
					More data for this Ligand-Target Pair