H-Met-OMe.HCl

Names

[ Name ]:
H-Met-OMe.HCl

[Synonym ]:
2-Thioxo-3-phenyl-5-isobutylimidazolidine-4-one
Methyl L-methioninate hydrochloride (1:1)
L-Methionine, methyl ester, hydrochloride (1:1)
PHENYLTHIOHYDANTOIN-LEUCINE
L-methionine methyl ester hydrochloride salt
methyl 2-amino-4-(methylthio)butanoate hydrochloride
D,L-methionine methyl ester hyfrochloride
H-MET-OME HYDROCHLORIDE
Methionine, methyl ester, hydrochloride (1:1)
PTH-L-LEUCINE
5-Isobutyl-3-phenyl-2-thioxo-imidazolidin-4-on
5-Isobutyl-3-phenyl-2-thioxo-4-imidazolidinone
H-Met-OMe.HCl
L-Methionine Methyl Ester HCl
OMe-methionine hydrochloride
H-L-Met-OMe*HCl
EINECS 219-651-9
5-ISOBUTYL-3-PHENYL-2-THIOHYDANTOIN
H-Met-Ome HCl
H-Met-OMe&H-MET-OME HCL
(2S)-1-methoxy-4-(methylsulfanyl)-1-oxobutan-2-aminium chloride
methyl (2S)-2-amino-4-(methylsulfanyl)butanoate hydrochloride
Methyl methioninate hydrochloride (1:1)
H-D-Met-OMeï¿½ï¿½HCl
MFCD00012491
Met-OMe.HCl
H-Met-OMe·HCl
3-Phenyl-5-isobutyl-thiohydantoin
H-DL-Met-OMe.HCl
L-Met methyl ester hydrochloride
methionine methyl ester hydrochloride
D,L-leucine N-phenylthiohydantoin
DL-methionine methyl ester hydrochloride
methyl L-methionate hydrochloride
L-Methionine Methyl Ester Hydrochloride
L-Methioninemethylesterhydrochloride
1-Phenyl-2-thioxo-4-isobutylimidazolidine-5-one
PTH-DL-LEUCINE
METHIONINE-OME HCL
5-Isobutyl-3-phenyl-thiohydantoin
Methyl L-methioninate hydrochloride
H-Met-OMeCl
5-isobutyl-3-phenyl-2-thioxo-imidazolidin-4-one
PTH-DL-Leucine Phenylthiohydantoin-DL-leucine
Leucine 3-phenyl-2-thiohydantoin
H-Met-Ome HCl

Biological Activity

[Description]:

L-Methionine methyl ester hydrochloride is a Methionine (HY-13694) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

[ Density]:
1.094g/cm3

[ Boiling Point ]:
277.6ºC at 760 mmHg

[ Melting Point ]:
151-153 °C(lit.)

[ Molecular Formula ]:
C₆H₁₄ClNO₂S

[ Molecular Weight ]:
199.699

[ Flash Point ]:
121.7ºC

[ Exact Mass ]:
199.043381

[ PSA ]:
77.62000

[ LogP ]:
1.74210

[ Vapour Pressure ]:
0.0388mmHg at 25°C

[ Index of Refraction ]:
26 ° (C=1, H2O)

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Novel molecular combination deriving from natural aminoacids and polyphenols: Design, synthesis and free-radical scavenging activities.

Eur. J. Med. Chem. 50 , 383-92, (2012)

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 ...