2-Aminophenol; N-Ac 

AlkaPlorer ID: AK019063

Synonym: 2-Acetamidophenol, 2-Hydroxyacetanilide, N-(2-Hydroxyphenyl)acetamide 

IUPAC Name: N-(2-hydroxyphenyl)acetamide

Structure

SMILES: CC(O)=NC1=CC=CC=C1O

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InChI: InChI=1S/C8H9NO2/c1-6(10)9-7-4-2-3-5-8(7)11/h2-5,11H,1H3,(H,9,10)

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InChIKey: ADVGKWPZRIDURE-UHFFFAOYSA-N

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Properties Information

Molecule Weight: 151.16499999999996

TPSA: 52.82000000000001

MolLogP: 2.0001

Number of H-Donors: 2

Number of H-Acceptors: 2

RingCount: 1

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Escherichia coli K-12 Beta-lactamase AmpC Potency 44668.4 nM None
Homo sapiens Bromodomain adjacent to zinc finger domain protein 2B Potency 100000.0 nM None
Homo sapiens Cholesterol 24-hydroxylase Activity 103.0 % None
Homo sapiens DNA-(apurinic or apyrimidinic site) lyase Potency 44668.4 nM None
Mus musculus RAW264.7 GI50 4204000.0 nM 10.1039/C3MD00251A
Mycobacterium tuberculosis Mycobacterium tuberculosis MIC 132000.0 nM 10.1039/C3MD00251A
Mycobacterium tuberculosis variant bovis BCG Mycobacterium tuberculosis variant bovis BCG MIC 132000.0 nM 10.1039/C3MD00251A
Mycolicibacterium smegmatis Mycolicibacterium smegmatis MIC 600000.0 nM 10.1039/C3MD00251A
Simian virus 40 Large T antigen IC50 6200.0 nM None
None Unchecked AC50 18440.0 nM None
None Unchecked IC50 2630.0 nM None
None Unchecked Potency 31622.8 nM None
None Unchecked Selectivity Index 31.8 None 10.1039/C3MD00251A

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT004746 CC(=O)[CoA].Nc1ccccc1O>>CC(=O)Nc1ccccc1O enzymemap_28550