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Details

Stereochemistry ABSOLUTE
Molecular Formula C3H6O3
Molecular Weight 90.0779
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCERALDEHYDE, D-

SMILES

OC[C@@H](O)C=O

InChI

InChIKey=MNQZXJOMYWMBOU-VKHMYHEASA-N
InChI=1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m0/s1

HIDE SMILES / InChI

Molecular Formula C3H6O3
Molecular Weight 90.0779
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Molecular and biochemical characterisation of human short-chain dehydrogenase/reductase member 3 (DHRS3).
2015-06-05
Triphenyltin impairs insulin secretion by decreasing glucose-induced NADP(H) and ATP production in hamster pancreatic β-cells.
2012-09-28
Cytotoxic molecular mechanisms and cytoprotection by enzymic metabolism or autoxidation for glyceraldehyde, hydroxypyruvate and glycolaldehyde.
2011-05-30
Functional expression of novel human and murine AKR1B genes.
2011-05-30
Hepatocyte or serum albumin protein carbonylation by oxidized fructose metabolites: Glyceraldehyde or glycolaldehyde as endogenous toxins?
2010-10-06
Synthesis of sialoglycopolypeptide for potentially blocking influenza virus infection using a rat alpha2,6-sialyltransferase expressed in BmNPV bacmid-injected silkworm larvae.
2009-06-05
Cancer biomarker AKR1B10 and carbonyl metabolism.
2009-03-16
Aldo-keto reductases from the AKR1B subfamily: retinoid specificity and control of cellular retinoic acid levels.
2009-03-16
Inhibiting wild-type and C299S mutant AKR1B10; a homologue of aldose reductase upregulated in cancers.
2008-04-28
Reduced 293T cell susceptibility to acrolein due to aldose reductase-like-1 protein expression.
2007-06
Aldehydes release zinc from proteins. A pathway from oxidative stress/lipid peroxidation to cellular functions of zinc.
2006-09
Stimulation of insulin release by glyceraldehyde may not be similar to glucose.
2006-03-15
Structure of the thermolabile mutant aldolase B, A149P: molecular basis of hereditary fructose intolerance.
2005-03-18
Serum or cerebrospinal fluid levels of glyceraldehyde-derived advanced glycation end products (AGEs) may be a promising biomarker for early detection of Alzheimer's disease.
2005
Glyceraldehyde-derived advanced glycation end products in Alzheimer's disease.
2004-09
Effect of carbonyl compounds on red blood cells deformability.
2004-08-27
8-Hydroxydaidzein, an aldose reductase inhibitor from okara fermented with Aspergillus sp. HK-388.
2004-07
Alternative routes for the formation of glyceraldehyde-derived AGEs (TAGE) in vivo.
2004
Metabolism, not autoxidation, plays a role in alpha-oxoaldehyde- and reducing sugar-induced erythrocyte GSH depletion: relevance for diabetes mellitus.
2003-10
Enhancement of chaperone function of alpha-crystallin by methylglyoxal modification.
2003-09-16
A flavone from Manilkara indica as a specific inhibitor against aldose reductase in vitro.
2003-09
A practical method to study functional impairment of proteins by glycation and effects of inhibitors using current coagulation/fibrinolysis reagent kits.
2003-03
Low molecular organic inactivators in differentiating organ origin of alpha-amylase in humans. Part I.
1989-10-01
Urine glyceraldehyde excretion is elevated in the renal Fanconi syndrome.
1989-01
Re-evaluation of the fructosamine reaction.
1988-08
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:45:59 GMT 2025
Edited
by admin
on Mon Mar 31 22:45:59 GMT 2025
Record UNII
41A680M0WB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCERALDEHYDE, D-
Systematic Name English
NSC-91534
Preferred Name English
PROPANAL, 2,3-DIHYDROXY-, (2R)-
Systematic Name English
D-(+)-GLYCERALDEHYDE
Common Name English
(R)-(+)-GLYCERALDEHYDE
Systematic Name English
(R)-GLYCERALDEHYDE
Systematic Name English
GLYCERALDEHYDE D-FORM [MI]
Common Name English
TRIOSE
Common Name English
Code System Code Type Description
FDA UNII
41A680M0WB
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID70196464
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
CHEBI
17378
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
PUBCHEM
79014
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-217-1
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
MERCK INDEX
m5787
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB02536
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
CAS
453-17-8
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
CHEBI
27137
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY
NSC
91534
Created by admin on Mon Mar 31 22:45:59 GMT 2025 , Edited by admin on Mon Mar 31 22:45:59 GMT 2025
PRIMARY