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Details

Stereochemistry ACHIRAL
Molecular Formula C2H4OS
Molecular Weight 76.118
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MERCAPTOACETALDEHYDE

SMILES

SCC=O

InChI

InChIKey=FLJWVVUJGVNXMZ-UHFFFAOYSA-N
InChI=1S/C2H4OS/c3-1-2-4/h1,4H,2H2

HIDE SMILES / InChI

Molecular Formula C2H4OS
Molecular Weight 76.118
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Removal of Cu2+ and turbidity from wastewater by mercaptoacetyl chitosan.
2009-09-30
Crystal structures of human SIRT3 displaying substrate-induced conformational changes.
2009-09-04
Systematic syntheses of influenza neuraminidase inhibitors: a series of carbosilane dendrimers uniformly functionalized with thioglycoside-type sialic acid moieties.
2009-08-01
Molecular orientation and field-effect transistors of a rigid rod conjugated polymer thin films.
2009-04-02
Ordering rigid rod conjugated polymer molecules for high performance photoswitchers.
2008-12-02
Deprotecting thioacetyl-terminated terphenyldithiol for assembly on gallium arsenide.
2008-02-05
Substituting N(epsilon)-thioacetyl-lysine for N(epsilon)-acetyl-lysine in peptide substrates as a general approach to inhibiting human NAD(+)-dependent protein deacetylases.
2008-01
Mechanism-based inhibition of Sir2 deacetylases by thioacetyl-lysine peptide.
2007-12-18
Synthesis of lipophilic 2-oxoamides based on gamma-aminobutyric and delta-aminovaleric analogues and their activity against phospholipase A2.
2007-10
Structural basis of spirolactone recognition by the mineralocorticoid receptor.
2007-09
Synthesis of L-beta-3'-deoxy-3',3'-difluoro-4'-thionucleosides.
2006-12-21
High-sensitivity transmission IR spectroscopy for the chemical identification and structural analysis of conjugated molecules on gallium arsenide surfaces.
2006-11-07
Synthesis and properties of an anthraquinone-based redox switch for molecular electronics.
2006-05-25
Monolayer-protected gold nanoparticle coalescence induced by photogenerated radicals.
2005-10-11
Synthesis of a dimeric Lewis antigen and the evaluation of the epitope specificity of antibodies elicited in mice.
2005-09-05
Bisubstrate analog probes for the insulin receptor protein tyrosine kinase: molecular yardsticks for analyzing catalytic mechanism and inhibitor design.
2005-08
The Met852 residue is a key organizer of the ligand-binding cavity of the human mineralocorticoid receptor.
2005-05
Pharmacokinetics and pharmacodynamics of mineralocorticoid blocking agents and their effects on potassium homeostasis.
2005-01
Utility of acetyldithio-CoA in detecting the influence of active site residues on substrate enolization by 3-hydroxyl-3-methylglutaryl-CoA synthase.
2004-09-24
The immunogenicity of the tumor-associated antigen Lewis(y) may be suppressed by a bifunctional cross-linker required for coupling to a carrier protein.
2004-07-19
AFM characterization of nanoscale ribbons grown from a series of oligo(p-phenyleneethynylene) derivatives.
2004-02-03
Synthesis of novel cyclic oligosaccharides: beta-1,6-thio-linked cycloglucopyranosides.
2002-12-12
Oligodeoxyribonucleotide analogues with bridging dimethylene sulfide, sulfoxide, and sulfone groups. Toward a second-generation model of nucleic acid structure.
2002-06-14
Conformational analysis of thiopeptides: free energy calculations on the effects of thio-substitutions on the conformational distributions of alanine dipeptides.
2001
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:58:08 GMT 2025
Edited
by admin
on Mon Mar 31 22:58:08 GMT 2025
Record UNII
M7I29I8T38
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MERCAPTOACETALDEHYDE
Systematic Name English
.ALPHA.-MERCAPTOACETALDEHYDE
Preferred Name English
ACETALDEHYDE, MERCAPTO-
Systematic Name English
Code System Code Type Description
PUBCHEM
77775
Created by admin on Mon Mar 31 22:58:08 GMT 2025 , Edited by admin on Mon Mar 31 22:58:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
223-929-5
Created by admin on Mon Mar 31 22:58:08 GMT 2025 , Edited by admin on Mon Mar 31 22:58:08 GMT 2025
PRIMARY
CAS
4124-63-4
Created by admin on Mon Mar 31 22:58:08 GMT 2025 , Edited by admin on Mon Mar 31 22:58:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID10194161
Created by admin on Mon Mar 31 22:58:08 GMT 2025 , Edited by admin on Mon Mar 31 22:58:08 GMT 2025
PRIMARY
FDA UNII
M7I29I8T38
Created by admin on Mon Mar 31 22:58:08 GMT 2025 , Edited by admin on Mon Mar 31 22:58:08 GMT 2025
PRIMARY