H-Tyr-OMe.HCl

Names

[ Name ]:
H-Tyr-OMe.HCl

[Synonym ]:
Methyl L-tyrosinate hydrochloride
L-Tyrosine Methylester HLC
L-TyrOCH3 hydrochloride
Tyr-OmeHCl
(S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester hydrochloride
methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate hydrochloride
METHYL TYROSINATE HCL
EINECS 222-313-3
Tyrosine methyl ester hydrochloride, L-
L-Tyrosine Methyl Ester Hydrochloride
TYROSINE-OME HCL
L-TYROSINE METHYL ESTER HCL
L-Tyrosine, methyl ester, hydrochloride (1:1)
H-L-TYR-OME HCL
H-Tyr-OMe·HCl
(S)-Methyl 2-amino-3-(4-hydroxyphenyl)propanoate hydrochloride
L-Tyrosine, methyl ester, hydrochloride
L-Tyr-OMe.HCL
MethylL-tyrosinatehydrochloride
L-Tyr-OMe hydrochloride
MFCD00012607
L-Tyr methyl ester hydrochloride
QR D1YZVO1 &&L Form HCl
L-Tyrosinemethylesterhydrochloride
Methyl L-tyrosinate hydrochloride (1:1)
H-Tyr-Ome HCl
H-Tyr-OMe.HCl

Biological Activity

[Description]:

H-Tyr-OMe.HCl is a tyrosine 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]:
1.21g/cm3

[ Boiling Point ]:
330ºC at 760 mmHg

[ Melting Point ]:
192 °C (dec.)(lit.)

[ Molecular Formula ]:
C₁₀H₁₄ClNO₃

[ Molecular Weight ]:
231.676

[ Flash Point ]:
153.4ºC

[ Exact Mass ]:
231.066223

[ PSA ]:
72.55000

[ LogP ]:
1.93730

[ Index of Refraction ]:
13 ° (C=2, MeOH)

[ Storage condition ]:
2~8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29225000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. 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 ...

Aromatic amino acid methyl ester analogs form quinonoidal species with Dopa decarboxylase.

FEBS Lett. 412(1) , 245-8, (1997)

This study reports for the first time that binding of aromatic methyl ester analogs to Dopa decarboxylase in the native and inactive nicked forms causes the appearance of a dead-end quinonoidal specie...