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Details

Stereochemistry ACHIRAL
Molecular Formula C4H8O2S
Molecular Weight 120.17
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-(METHYLTHIO)PROPIONIC ACID

SMILES

CSCCC(O)=O

InChI

InChIKey=CAOMCZAIALVUPA-UHFFFAOYSA-N
InChI=1S/C4H8O2S/c1-7-3-2-4(5)6/h2-3H2,1H3,(H,5,6)

HIDE SMILES / InChI

Molecular Formula C4H8O2S
Molecular Weight 120.17
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
1+1 = 3: a fusion of 2 enzymes in the methionine salvage pathway of Tetrahymena thermophila creates a trifunctional enzyme that catalyzes 3 steps in the pathway.
2009-10
Nickel-based Enzyme Systems.
2009-07-10
Production of the aroma chemicals 3-(methylthio)-1-propanol and 3-(methylthio)-propylacetate with yeasts.
2008-09
L-methionine toxicity in freshly isolated mouse hepatocytes is gender-dependent and mediated in part by transamination.
2008-09
Pathways that produce volatile sulphur compounds from methionine in Oenococcus oeni.
2008-06
3-Methylthiopropionic acid ethyl ester, isolated from Katsura-uri (Japanese pickling melon, Cucumis melo var. conomon), enhanced differentiation in human colon cancer cells.
2008-05-14
Characterization of metal binding in the active sites of acireductone dioxygenase isoforms from Klebsiella ATCC 8724.
2008-02-26
Production of the apoptotic cellular mediator 4-Methylthio-2-oxobutyric acid by using an enzymatic stirred tank reactor with in situ product removal.
2007-12-21
One protein, two enzymes revisited: a structural entropy switch interconverts the two isoforms of acireductone dioxygenase.
2006-11-03
Bacterial taxa that limit sulfur flux from the ocean.
2006-10-27
Synthesis and effects of 3-methylthiopropanoyl thiolesters of lipoic acid, methional metabolite mimics.
2006-02
Alcohols, esters and heavy sulphur compounds production by pure and mixed cultures of apiculate wine yeasts.
2005-09-15
Analogs of 1-phosphonooxy-2,2-dihydroxy-3-oxo-5-(methylthio)pentane, an acyclic intermediate in the methionine salvage pathway: a new preparation and characterization of activity with E1 enolase/phosphatase from Klebsiella oxytoca.
2004-07-15
Bacterial variations on the methionine salvage pathway.
2004-03-04
Methionine catabolism and production of volatile sulphur compounds by OEnococcus oeni.
2004
3-methylthiopropanoic acid produced by Enterobacter intermedium 60-2G inhibits fungal growth and weed seedling development.
2003-02
How low pH can intensify beta-damascenone and dimethyl trisulfide production through beer aging.
2002-09-25
Modification of the swern oxidation: use of a recyclable, polystyrene bound sulfoxide.
2002-07-22
XAS investigation of the structure and function of Ni in acireductone dioxygenase.
2002-05-28
Anticonvulsant activity of N-palmitoylethanolamide, a putative endocannabinoid, in mice.
2001-03
Urinary 3-methylthiopropionate excretion and the effect of D- or L-methionine ingestion studied in healthy subjects.
1987-04
[Analysis of methionine metabolism studied by the gas chromatographic determination of 3-methylthiopropionate in urine and its clinical application].
1985-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:59:34 GMT 2025
Edited
by admin
on Mon Mar 31 20:59:34 GMT 2025
Record UNII
F523ALI47D
Record Status Validated (UNII)
Record Version
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Name Type Language
3-METHYLTHIOPROPIONA
Preferred Name English
3-(METHYLTHIO)PROPIONIC ACID
Systematic Name English
3-METHYLSULFANYLPROPIONIC ACID
Systematic Name English
3-(METHYLTHIO)PROPANOIC ACID
Systematic Name English
PROPANOIC ACID, 3-(METHYLTHIO)-
Common Name English
3-(METHYLMERCAPTO)PROPANOIC ACID
Systematic Name English
3-(METHYLMERCAPTO)PROPIONIC ACID
Systematic Name English
Code System Code Type Description
CAS
646-01-5
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID70862354
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
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PUBCHEM
563
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-460-9
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
PRIMARY
FDA UNII
F523ALI47D
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
PRIMARY
CHEBI
1438
Created by admin on Mon Mar 31 20:59:34 GMT 2025 , Edited by admin on Mon Mar 31 20:59:34 GMT 2025
PRIMARY