H-Tyr-ObzlTos

Names

[ Name ]:
H-Tyr-ObzlTos

[Synonym ]:
H-Tyr-OBzl.TosOH
H-Tyr-OBzl·Tos-OH
MFCD00038959
EINECS 258-650-8
Benzyl tyrosinate 4-methylbenzenesulfonate (1:1)
L-Tyrosine Benzyl Ester p-Toluenesulfonate
Tyr-OBzl TosOH
L-Tyrosine, O-(phenylmethyl)-, 4-methylbenzenesulfonate (1:1)
O-Benzyl-L-tyrosine 4-methylbenzenesulfonate (1:1)
benzyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate,4-methylbenzenesulfonic acid
Tyrosine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)
(S)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoate 4-methylbenzenesulfonate
H-TYR-OBZL·TOS
H-Tyr-ObzlTos

Biological Activity

[Description]:

H-Tyr-OBzl.TosOH 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

[ Boiling Point ]:
438.7ºC at 760 mmHg

[ Melting Point ]:
177 °C

[ Molecular Formula ]:
C₂₃H₂₅NO₆S

[ Molecular Weight ]:
443.513

[ Flash Point ]:
359.8ºC

[ Exact Mass ]:
443.140259

[ PSA ]:
135.30000

[ LogP ]:
5.02820

[ Index of Refraction ]:
-13 ° (C=3, MeOH)

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Effect of protease inhibitors and substrates on 3,5,3'-triiodothyronine binding to rat liver nuclear receptors.

Endocr. Regul. 26 , 127-131, (1992)

The effect of protease inhibitors N-tosyl-L-phenylalanine chloromethyl ketone (TPCK) and N-carbobenzoxy-L-phenylalanine chloromethyl ketone (ZPCK) at concentrations ranging from 1.5 x 10(-6) mol/l to ...

Endosperm-specific expression of tyramine N-hydroxycinnamoyltransferase and tyrosine decarboxylase from a single self-processing polypeptide produces high levels of tyramine derivatives in rice seeds.

Biotechnol. Lett. 31 , 911-915, (2009)

The plant-specific tyramine derivatives, feruloyltyramine (FT) and 4-coumaroyltyramine (CT), represent bioactive compounds found at low levels in many plant species. We generated transgenic rice seeds...

Purification, characterization and partial amino acid sequencing of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase from tobacco cell-suspension cultures.

Eur. J. Biochem. 247 , 1127-1135, (1997)

We report the purification of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase (THT) to apparent homogeneity in 12% yield from tobacco (Nicotiana tabacum L. cv. Xanthi) cell-suspension cu...