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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
Re-evaluation of the fructosamine reaction.
1988 Aug
A practical method to study functional impairment of proteins by glycation and effects of inhibitors using current coagulation/fibrinolysis reagent kits.
2003 Mar
Metabolism, not autoxidation, plays a role in alpha-oxoaldehyde- and reducing sugar-induced erythrocyte GSH depletion: relevance for diabetes mellitus.
2003 Oct
A flavone from Manilkara indica as a specific inhibitor against aldose reductase in vitro.
2003 Sep
Enhancement of chaperone function of alpha-crystallin by methylglyoxal modification.
2003 Sep 16
Glyceraldehyde-derived advanced glycation end products in Alzheimer's disease.
2004 Sep
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
Cancer biomarker AKR1B10 and carbonyl metabolism.
2009 Mar 16
Hepatocyte or serum albumin protein carbonylation by oxidized fructose metabolites: Glyceraldehyde or glycolaldehyde as endogenous toxins?
2010 Oct 6
Cytotoxic molecular mechanisms and cytoprotection by enzymic metabolism or autoxidation for glyceraldehyde, hydroxypyruvate and glycolaldehyde.
2011 May 30
Functional expression of novel human and murine AKR1B genes.
2011 May 30
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:38:00 GMT 2023
Edited
by admin
on Sat Dec 16 09:38:00 GMT 2023
Record UNII
41A680M0WB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCERALDEHYDE, D-
Systematic 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
NSC-91534
Code English
TRIOSE
Common Name English
Code System Code Type Description
FDA UNII
41A680M0WB
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
EPA CompTox
DTXSID70196464
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
CHEBI
17378
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
PUBCHEM
79014
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-217-1
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
MERCK INDEX
m5787
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB02536
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
CAS
453-17-8
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
CHEBI
27137
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY
NSC
91534
Created by admin on Sat Dec 16 09:38:00 GMT 2023 , Edited by admin on Sat Dec 16 09:38:00 GMT 2023
PRIMARY