Page last updated: 2024-12-05

methionol

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

methionol: a aroma-active compound [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

3-methylthiopropanol : An alkyl sulfide that is propan-1-ol substituted by a methylsulfanyl group at position 3. It is a volatile compound found in wines and produced during fermentation. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID10448
CHEMBL ID332887
CHEBI ID49019
SCHEMBL ID101773
MeSH IDM0554378

Synonyms (62)

Synonym
3-methylmercapto-1-propanol
3-(methylthio)-1-propanol
nsc-2859
nsc2859
3-hydroxypropyl methyl sulfide
.gamma.-methylmercaptopropyl alcohol
methionol
1-propanol, 3-(methylthio)-
505-10-2
inchi=1/c4h10os/c1-6-4-2-3-5/h5h,2-4h2,1h
3-(methylthio)propyl alcohol
3-methylthiopropanol
CHEBI:49019 ,
gamma-methylmercaptopropyl alcohol
3-(methylsulfanyl)propan-1-ol
3-(methylthio)-1-propanol, >=98%, fg
3-(methylthio)-1-propanol, 98%
3-methylsulfanyl-1-propanol
methylmercaptopropanol
3-methylsulfanylpropan-1-ol
CHEMBL332887
3-methylthio-1-propanol
3-methylmercaptopropyl alcohol
M0735
AKOS005255124
3-(methylsulfanyl)-1-propanol
A828145
ai3-17420
3-(methylthio)propanol
nsc 2859
unii-h1e1u441xx
h1e1u441xx ,
fema no. 3415
einecs 208-004-6
methyl 3-hydroxypropylsulfide
gamma-hydroxypropyl methyl sulfide
FT-0602452
4-thiapentan-1-ol
3-(methylthio)propan-1-ol
SCHEMBL101773
3-(methylthio)propanol [fhfi]
3-methylsulfanyl-propan-1-ol
3-(methylthio)propane-1-ol
DTXSID7060128
3-(methylsulfanyl)propanol
3-(methylsulfanyl)-1-propanol #
3-methylthiopropyl alcohol
Q-100564
J-640445
J-800459
c4h10os
mfcd00036560
AS-59057
laquo gammaraquo -methylmercaptopropyl alcohol
fema 3415
3-(methylsulfanyl)propanol (methionol)
Q11343729
EN300-112112
SB17653
3-hydroxypropyl methyl sulfide; 3-methylmercapto-1-propanol; 4-thiapentan-1-ol
3-(methylmercapto)propan-1-ol
CS-0015993

Research Excerpts

Overview

Methionol is an important volatile sulfur flavor compound. It can be produced via the Ehrlich pathway in Saccharomyces cerevisiae.

ExcerptReferenceRelevance
"Methionol is an important volatile sulfur flavor compound, which can be produced via the Ehrlich pathway in Saccharomyces cerevisiae. "( Significant enhancement of methionol production by co-expression of the aminotransferase gene ARO8 and the decarboxylase gene ARO10 in Saccharomyces cerevisiae.
Lang, T; Liu, L; Sun, B; Wang, C; Xiao, X; Yin, S, 2015
)
2.16
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
aliphatic sulfide
methyl sulfideAny aliphatic sulfide in which at least one of the organyl groups attached to the sulfur is a methyl group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (3)

PathwayProteinsCompounds
methanogenesis from dimethylsulfide27
L-methionine degradation III811
methionine degradation III1210

Bioassays (1)

Assay IDTitleYearJournalArticle
AID222181Ability to inhibit Escherichia coli methionyl-tRNA synthetase was determined at a concentration of 270 uM1998Bioorganic & medicinal chemistry letters, Dec-15, Volume: 8, Issue:24
Methionine analogues as inhibitors of methionyl-tRNA synthetase.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (14)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (7.14)18.2507
2000's3 (21.43)29.6817
2010's9 (64.29)24.3611
2020's1 (7.14)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.74

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index30.74 (24.57)
Research Supply Index2.71 (2.92)
Research Growth Index5.10 (4.65)
Search Engine Demand Index36.71 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.74)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other14 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]