U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C2H4O
Molecular Weight 44.0526
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETALDEHYDE

SMILES

CC=O

InChI

InChIKey=IKHGUXGNUITLKF-UHFFFAOYSA-N
InChI=1S/C2H4O/c1-2-3/h2H,1H3

HIDE SMILES / InChI

Molecular Formula C2H4O
Molecular Weight 44.0526
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Acetaldehyde enhances murine alpha2(I) collagen promoter activity by Ca2+-independent protein kinase C activation in cultured rat hepatic stellate cells.
1999 Feb
Acetaldehyde increases the activity and gene expression of urokinase type plasminogen activator in a hepatic stellate cell line.
1999 Sep 10
Hydrogen peroxide: a link between acetaldehyde-elicited alpha1(I) collagen gene up-regulation and oxidative stress in mouse hepatic stellate cells.
2000 Jan
Modification and inhibition of vancomycin group antibiotics by formaldehyde and acetaldehyde.
2001
[Volatile compounds in air and oral saliva in healthy people, and in periodontitis and gingivitis patients].
2001
Aldehydes potentiate alpha(2)(I) collagen gene activity by JNK in hepatic stellate cells.
2001 Apr 15
Platelet-activating factor acetylhydrolases: broad substrate specificity and lipoprotein binding does not modulate the catalytic properties of the plasma enzyme.
2001 Apr 17
First total synthesis of phenylpyridine analogues of the antimitotic rhazinilam.
2001 Apr 20
Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile.
2001 Feb
Effect of carbohydrate substrate on fermentation by kefir yeast supported on delignified cellulosic materials.
2001 Feb
No correlation between wine intolerance and histamine content of wine.
2001 Feb
Poor dental status increases acetaldehyde production from ethanol in saliva: a possible link to increased oral cancer risk among heavy drinkers.
2001 Feb
Involvement of acetyl phosphate in the in vivo activation of the response regulator ComA in Bacillus subtilis.
2001 Feb 20
Ethanol infusion increases ANP and p21 gene expression in isolated perfused rat heart.
2001 Feb 23
Physical association between the histone acetyl transferase CBP and a histone methyl transferase.
2001 Jan
Characterizing colloidal structures of pseudoternary phase diagrams formed by oil/water/amphiphile systems.
2001 Jan
Prodrugs of butyric acid. Novel derivatives possessing increased aqueous solubility and potential for treating cancer and blood diseases.
2001 Jan
Ornithinimicrobium humiphilum gen. nov., sp. nov., a novel soil actinomycete with L-ornithine in the peptidoglycan.
2001 Jan
Biphasic effects of acetaldehyde-biogenic amine condensation products on membrane fluidity.
2001 Jan
Iron-induced changes in pyruvate metabolism of Tritrichomonas foetus and involvement of iron in expression of hydrogenosomal proteins.
2001 Jan
Effect of cigarette smoke extract on neonatal porcine vascular smooth muscle cells.
2001 Jan 15
Enhanced reactivity of 2-rhodaoxetanes through a labile acetonitrile ligand.
2001 Jan 19
Prothymosin alpha functions as a cellular oncoprotein by inducing transformation of rodent fibroblasts in vitro.
2001 Jan 19
Biogenic aldehyde(s) derived from the action of monoamine oxidase may mediate the antidipsotropic effect of daidzin.
2001 Jan 30
[Acetyl starch as volume substitute, a possible alternative to HES].
2001 Jan 5
The transcriptional and DNA binding activity of peroxisome proliferator-activated receptor alpha is inhibited by ethanol metabolism. A novel mechanism for the development of ethanol-induced fatty liver.
2001 Jan 5
Intragastric ethanol infusion model for cellular and molecular studies of alcoholic liver disease.
2001 Jan-Feb
Effects of chronic metrifonate treatment on cholinergic enzymes and the blood-brain barrier.
2001 Jul
Flavor threshold for acetaldehyde in milk, chocolate milk, and spring water using solid phase microextraction gas chromatography for quantification.
2001 Mar
Alcohol dehydrogenase 3 genotype is not associated with risk of squamous cell carcinoma of the oral cavity and pharynx.
2001 Mar
Acetaldehyde production and other ADH-related characteristics of aerobic bacteria isolated from hypochlorhydric human stomach.
2001 Mar
Age-related changes in the urinary excretion of aldehydes in ad libitum fed and food-restricted rats.
2001 Mar
Stable histone deacetylase complexes distinguished by the presence of SANT domain proteins CoREST/kiaa0071 and Mta-L1.
2001 Mar 2
Regulation of the aldehyde dehydrogenase gene (aldA) and its role in the control of the coinducer level necessary for induction of the ethanol utilization pathway in Aspergillus nidulans.
2001 Mar 9
Paradoxical effects of trichostatin A: inhibition of NF-Y-associated histone acetyltransferase activity, phosphorylation of hGCN5 and downregulation of cyclin A and B1 mRNA.
2001 May 10
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:32 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:32 GMT 2023
Record UNII
GO1N1ZPR3B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETALDEHYDE
FCC   FHFI   HPUS   HSDB   INCI   MI  
INCI  
Official Name English
ACETALDEHYDE [IARC]
Common Name English
Acetaldehyde [WHO-DD]
Common Name English
VINYL ALCOHOL (FROM ALCOHOLYSIS OR HYDROLYSIS OF VINYL ACETATE UNITS)
Common Name English
ETHYLALDEHYDE
Common Name English
ETHENOL
Systematic Name English
HYDROXYETHYLENE
Systematic Name English
NSC-7594
Code English
ACETALDEHYDE [MI]
Common Name English
ACETALDEHYDE [HPUS]
Common Name English
VINYL ALCOHOL
Systematic Name English
CARMUSTINE RELATED COMPOUND, ACETALDEHYDE-
Common Name English
ETHANAL
Systematic Name English
ACETALDEHYDE [FCC]
Common Name English
HYDROXYETHENE
Systematic Name English
ACETALDEHYDE [FHFI]
Common Name English
ACETALDEHYDE [USP-RS]
Common Name English
FEMA NO. 2003
Code English
ACETALDEHYDE [HSDB]
Common Name English
ACETALDEHYDE [INCI]
Common Name English
ACETIC ALDEHYDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45175
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
JECFA EVALUATION ACETALDEHYDE
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
NCI_THESAURUS C94714
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
IARC Acetaldehyde
EPA PESTICIDE CODE 202300
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
Code System Code Type Description
FDA UNII
GO1N1ZPR3B
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
WIKIPEDIA
ACETALDEHYDE
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
CAS
557-75-5
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
ALTERNATIVE
NCI_THESAURUS
C44328
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
NSC
7594
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
HSDB
230
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
CAS
75-07-0
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
PUBCHEM
177
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
200-836-8
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
CHEBI
15343
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID8051467
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
EVMPD
SUB106813
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
MESH
D000079
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-183-3
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
ALTERNATIVE
RXCUI
1311137
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY RxNorm
RS_ITEM_NUM
1002811
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
MERCK INDEX
m1310
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY Merck Index
SMS_ID
100000141981
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
DAILYMED
GO1N1ZPR3B
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
JECFA MONOGRAPH
2
Created by admin on Fri Dec 15 15:02:32 GMT 2023 , Edited by admin on Fri Dec 15 15:02:32 GMT 2023
PRIMARY
Related Record Type Details
METABOLIC ENZYME -> SUBSTRATE
PARENT -> CONSTITUENT ALWAYS PRESENT
Related Record Type Details
PARENT -> METABOLITE
PARENT -> METABOLITE TOXIC
METABOLITE -> PARENT
Related Record Type Details
PARENT -> IMPURITY