BDBM50363635 CHEMBL1945914

SMILES: CCCc1nccn1CC(=O)c1ccc(cc1)[N+]([O-])=O

InChI Key: InChIKey=STOXYEOEBXPVBA-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50363635   

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, brain (Rattus norvegicus (rat))	BDBM50363635 (CHEMBL1945914) Show SMILES CCCc1nccn1CC(=O)c1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C14H15N3O3/c1-2-3-14-15-8-9-16(14)10-13(18)11-4-6-12(7-5-11)17(19)20/h4-9H,2-3,10H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Catania Curated by ChEMBL					Assay Description Inhibition of rat recombinant nNOS expressed in baculovirus-infected Sf9 cells assessed as conversion of oxyhemoglobin to methemoglobin by UV spectro...				Eur J Med Chem 49: 118-26 (2012) Article DOI: 10.1016/j.ejmech.2012.01.002 BindingDB Entry DOI: 10.7270/Q2416XHC
					More data for this Ligand-Target Pair
Nitric-oxide synthase, endothelial (Mus musculus)	BDBM50363635 (CHEMBL1945914) Show SMILES CCCc1nccn1CC(=O)c1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C14H15N3O3/c1-2-3-14-15-8-9-16(14)10-13(18)11-4-6-12(7-5-11)17(19)20/h4-9H,2-3,10H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Catania Curated by ChEMBL					Assay Description Inhibition of C57BL/6 mouse eNOS assessed as conversion of oxyhemoglobin to methemoglobin by UV spectrophotometer analysis				Eur J Med Chem 49: 118-26 (2012) Article DOI: 10.1016/j.ejmech.2012.01.002 BindingDB Entry DOI: 10.7270/Q2416XHC
					More data for this Ligand-Target Pair