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SMILES: Cc1nc2ccc(cc2[nH]1)[N+]([O-])=O

InChI Key: InChIKey=RKRXTVLCZDPERO-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50404900   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Cytochrome P450 2B1


(Rattus norvegicus)		BDBM50404900
PNG
(CHEMBL353026)
Show SMILES Cc1nc2ccc(cc2[nH]1)[N+]([O-])=O
Show InChI InChI=1S/C8H7N3O2/c1-5-9-7-3-2-6(11(12)13)4-8(7)10-5/h2-4H,1H3,(H,9,10)
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CHEMBL
MCE
PC cid
PC sid
UniChem

Similars
PubMed
n/an/a 2.19E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory potency to aminopyrine N-demethylase activity (P450) in hepatic microsomes from phenobarbitone-induced rats.

J Med Chem 25: 887-92 (1982)


BindingDB Entry DOI: 10.7270/Q2VT1T8J
More data for this
Ligand-Target Pair