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860409

Sigma-Aldrich

L-Methionine methyl ester hydrochloride

98%

Synonym(s):

L-Met-OMe·HCl

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About This Item

Linear Formula:
CH3SCH2CH2CH(NH2)COOCH3 · HCl
CAS Number:
2491-18-1
Molecular Weight:
199.70
Beilstein:
3913214
EC Number:
219-651-9
MDL number:
MFCD00012491
UNSPSC Code:
12352209
PubChem Substance ID:
24888509
NACRES:
NA.22

Quality Level

200

Assay

98%

form

powder

optical activity

[α]22/D +25.9°, c = 1 in H2O

reaction suitability

reaction type: solution phase peptide synthesis

mp

151-153 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cl[H].COC(=O)[C@@H](N)CCSC

InChI

1S/C6H13NO2S.ClH/c1-9-6(8)5(7)3-4-10-2;/h5H,3-4,7H2,1-2H3;1H/t5-;/m0./s1

InChI key

MEVUPUNLVKELNV-JEDNCBNOSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Mark M Yore et al.
Cell, 159(2), 318-332 (2014-10-11)
Increased adipose tissue lipogenesis is associated with enhanced insulin sensitivity. Mice overexpressing the Glut4 glucose transporter in adipocytes have elevated lipogenesis and increased glucose tolerance despite being obese with elevated circulating fatty acids. Lipidomic analysis of adipose tissue revealed the
Matthew J Kolar et al.
Biochemistry, 55(33), 4636-4641 (2016-08-11)
A recently discovered class of endogenous mammalian lipids, branched fatty acid esters of hydroxy fatty acids (FAHFAs), possesses anti-diabetic and anti-inflammatory activities. Here, we identified and validated carboxyl ester lipase (CEL), a pancreatic enzyme hydrolyzing cholesteryl esters and other dietary
Vertuani Silvia et al.
European journal of medicinal chemistry, 50, 383-392 (2012-03-06)
Following the recent output of scientific publications in the matter of synergic activity between different antioxidants, we have undertaken the present study with the aim to synthesize new molecules with radical-scavengers activity based on the conjugation of bioactive portions (i.e.
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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