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Details

Stereochemistry ACHIRAL
Molecular Formula C8H9NO
Molecular Weight 135.1632
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENACYLAMINE

SMILES

NCC(=O)C1=CC=CC=C1

InChI

InChIKey=HEQOJEGTZCTHCF-UHFFFAOYSA-N
InChI=1S/C8H9NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6,9H2

HIDE SMILES / InChI

Molecular Formula C8H9NO
Molecular Weight 135.1632
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: 403149.0
Gene Symbol: CYP2A19
Target ID: P79383
Gene ID: 403216.0
Gene Symbol: CYP2E1
Target Organism: Sus scrofa (Pig)
PubMed

PubMed

TitleDatePubMed
2-Aminoacetophenone as a potential breath biomarker for Pseudomonas aeruginosa in the cystic fibrosis lung.
2010-11-07
N-[2-(4-Methyl-2-quinol-yl)phen-yl]acetamide: a P1 structure with Z = 4.
2010-07-17
N'-[1-(2-Amino-phen-yl)ethyl-idene]benzo-hydrazide.
2010-04-24
Identification, Cloning, and Characterization of l-Phenylserine Dehydrogenase from Pseudomonas syringae NK-15.
2010-03-25
(E)-N-{2-[1-(Benzyl-imino)eth-yl]phen-yl}benzamide.
2010-03-03
Design of a versatile multicomponent reaction leading to 2-amino-5-ketoaryl pyrroles.
2010-03
Silica gel-catalyzed one-pot syntheses in water and fluorescence properties studies of 5-amino-2-aryl-3H-chromeno[4,3,2-de][1,6]naphthyridine-4-carbonitriles and 5-amino-2-aryl-3H-quinolino[4,3,2-de][1,6]naphthyridine-4-carbonitriles.
2009-12-23
Glycosylation of aromatic amines III: Mechanistic implications of the pH-dependent glycosylation of various aromatic amines (kynurenine, 2'-aminoacetophenone, daptomycin, and sulfamethoxzaole).
2009-12
3-(2-Acetyl-anilino)propanoic acid.
2008-11-13
Purification and characterization of 2-aminoacetophenone reductase of newly isolated Burkholderia sp. YT.
2007-11
Sensitization of europium(III) luminescence by benzophenone-containing ligands: regioisomers, rearrangements and chelate ring size, and their influence on quantum yields.
2007-10-29
Use of liquid chromatography-mass spectrometry and a chemical cleavage reaction for the structure elucidation of a new sildenafil analogue detected as an adulterant in an herbal dietary supplement.
2007-08-15
Analysis of 2-aminoacetophenone in wine using a stable isotope dilution assay and multidimensional gas chromatography-mass spectrometry.
2007-05-25
Aroma components of acid-hydrolyzed vegetable protein made by partial hydrolysis of rice bran protein.
2007-04-18
Volatile composition and contribution to the aroma of spanish honeydew honeys. Identification of a new chemical marker.
2006-06-28
Reduction of stale flavor development in low-heat skim milk powder via epicatechin addition.
2006-01-25
Putative chemosignals of the ferret (Mustela furo) associated with individual and gender recognition.
2005-11
An advantageous route to oxcarbazepine (trileptal) based on palladium-catalyzed arylations free of transmetallating agents.
2005-10-27
Behavioural response of Triatoma infestans (Klug) (Hemiptera: Reduviidae) to quinazolines.
2005-09-30
[Synthesis and antitumor activity of arylsubstituted imidazolin-2-one derivatives].
2005-08
Evaluation of sample recovery of malodorous livestock gases from air sampling bags, solid-phase microextraction fibers, Tenax TA sorbent tubes, and sampling canisters.
2005-08
Synthetic applicability and in situ recycling of a B-methoxy oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol.
2004-08-05
Transformation of 2-aminoacetophenone to ( S) -2-amino-1-phenylethanol by Arthrobacter sulfureus.
2004-08
Characteristic aroma components of rennet casein.
2003-11-05
Possible coding for recognition of sexes, individuals and species in anal gland volatiles of Mustela eversmanni and M. sibirica.
2003-06
Phase II in vitro metabolism of 3-methylindole metabolites in porcine liver.
2003-05
Determination of cathinone, cathine and norephedrine in hair of Yemenite khat chewers.
2003-04-23
Analysis of ketones by selected ion flow tube mass spectrometry.
2003
Synthesis and cytotoxic evaluation of analogues of the marine pyridoacridine amphimedine.
2002-09
"Untypical aging off-flavor" in wine: synthesis of potential degradation compounds of indole-3-acetic acid and kynurenine and their evaluation as precursors of 2-aminoacetophenone.
2002-07-17
New entry of coupling reaction of phenacylamine derivatives with silylstannane.
2002-03
Comparison of key aroma compounds in cooked brown rice varieties based on aroma extract dilution analyses.
2002-02-27
Volatile flavor components of stored nonfat dry milk.
2002-01-16
Determination of free and conjugated indole-3-acetic acid, tryptophan, and tryptophan metabolites in grape must and wine.
2001-11
[Isolation and fermentation conditions of strains producing 1-phenyl-2-amino-ethanol alcohol dehydrogenase].
2001-10
Quantitative gas chromatography-olfactometry carried out at different dilutions of an extract. Key differences in the odor profiles of four high-quality Spanish aged red wines.
2001-10
[Studies on asymmetric synthesis of R-phenylethanolamine by whole cells of Arachnia sp. P163].
2001-07
Palatability of bird repellents to Rattus norvegicus.
2001-07
Aroma-active components of nonfat dry milk.
2001-06
Pyriform cortex beta-waves: odor-specific sensitization following repeated olfactory stimulation.
2001-02-23
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:21:48 GMT 2025
Edited
by admin
on Mon Mar 31 21:21:48 GMT 2025
Record UNII
4M571C83H7
Record Status Validated (UNII)
Record Version
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Name Type Language
.ALPHA.-DEMETHYLCATHINONE
Preferred Name English
PHENACYLAMINE
MI  
Systematic Name English
.OMEGA.-AMINOACETOPHENONE
Systematic Name English
ACETOPHENONE, 2-AMINO-
Systematic Name English
2-OXOPHENETHYLAMINE
Systematic Name English
(2-OXO-2-PHENYLETHYL)AMINE
Systematic Name English
2-OXO-2-PHENYLETHANAMINE
Systematic Name English
1-PHENYL-2-AMINOETHANONE
Systematic Name English
PHENACYLAMINE [MI]
Common Name English
ACETOPHENONE, .ALPHA.-AMINO-
Systematic Name English
2-AMINO-1-PHENYLETHANONE
Systematic Name English
2-AMINOACETOPHENONE
Systematic Name English
.ALPHA.-AMINOACETOPHENONE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 2-AMINOACETOPHENONE
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID80210206
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-358-1
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY
CAS
613-89-8
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY
FDA UNII
4M571C83H7
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY
MERCK INDEX
m8591
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY Merck Index
PUBCHEM
11952
Created by admin on Mon Mar 31 21:21:48 GMT 2025 , Edited by admin on Mon Mar 31 21:21:48 GMT 2025
PRIMARY