TYROSINE ETHYL ESTER HYDROCHLORIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C11H15NO3.ClH
Molecular Weight	245.703
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of TYROSINE ETHYL ESTER HYDROCHLORIDE

Structure Search

SMILES

Cl.CCOC(=O)[C@@H](N)CC1=CC=C(O)C=C1

InChI

InChIKey=BQULAXAVRFIAHN-PPHPATTJSA-N

InChI=1S/C11H15NO3.ClH/c1-2-15-11(14)10(12)7-8-3-5-9(13)6-4-8;/h3-6,10,13H,2,7,12H2,1H3;1H/t10-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	C11H15NO3
Molecular Weight	209.2417
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.fishersci.com/shop/products/l-tyrosine-ethyl-ester-hydrochloride-99-1/AAA1835814 | https://www.genome.jp/dbget-bin/www_bget?dr:D09821

Tyrosine ethyl ester hydrochloride is used as a medical and organic intermediate and as an important amino protective agent. It is also used to introduce t-Boc protect gene. Tyrosine ethyl ester hydrochloride is used as a supplement (tyrosine).

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
thyroid hormone receptor binding 2 Target ID: GO:0046966 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1308155	Inhibitor 8504

PubMed

Title	Date	PubMed
A thermodynamically consistent phase diagram of a trimorphic pharmaceutical, l-tyrosine ethyl ester, based on limited experimental data.	2018-09-26	30204172
Mechanism of papain-catalyzed synthesis of oligo-tyrosine peptides.	2015-01-30	26047910
High level production of bioactive di- and tri-tyrosine peptides by protease-catalyzed reactions.	2010-11	20868710
Probing molecular motion by double-quantum (13C,13C) solid-state NMR spectroscopy: application to ubiquitin.	2010-01-13	20000710
Singlet molecular oxygen [O2(1Deltag)]-mediated photodegradation of tyrosine derivatives in the presence of cationic and neutral micellar systems.	2008-06	17619119
Synthesis of gossypol atropisomers and derivatives and evaluation of their anti-proliferative and anti-oxidant activity.	2005-07-01	15878283
Light-driven tyrosine radical formation in a ruthenium-tyrosine complex attached to nanoparticle TiO2.	2002-12-02	12444768
Synthesis of 2-[18F]fluoro-L-tyrosine via regiospecific fluoro-de-stannylation.	2002-08	12150277
Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: synthesis of verongamine and purealidin N.	2001-05-04	11325276
BIOSYNTHESIS OF L-TYROSINE O-SULPHATE FROM THE METHYL AND ETHYL ESTERS OF L-TYROSINE.	1965-02	14348193

Patents

Sample Use Guides

In Vivo Use Guide

When male Sprague-Dawley rats were treated with 50 mg/kg L-tryptophan and Tyrosine ethyl ester 30 min prior to the intrahypothalamic injection of 2 ug amylin, brain tryptophan and tyrosine levels were selectively increased as compared to rats treated with amylin alone.

Route of Administration: Intraperitoneal

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:33:46 GMT 2025` Edited by `admin` on `Mon Mar 31 21:33:46 GMT 2025`
Record UNII	FAP58DAZ1E
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

TYROSINE ETHYL ESTER HYDROCHLORIDE

Systematic Name

English

L-TYROSINE ETHYLESTER MONOHYDROCHLORIDE

Preferred Name

English

L-TYROSINE ETHYLESTER MONOHYDROCHLORIDE [JAN]

Common Name

English

L-TYROSINE, ETHYL ESTER, HYDROCHLORIDE (1:1)

Common Name

English

(S)-(-)-TYROSINE ETHYL ESTER HYDROCHLORIDE

Systematic Name

English

ETHYL L-TYROSINATE HYDROCHLORIDE

Systematic Name

English

NSC-17141

Code

English

TYROSINE, ETHYL ESTER, HYDROCHLORIDE, L-

Common Name

English

L-TYROSINE, ETHYL ESTER, HYDROCHLORIDE

Common Name

English

L - TYROSINE ETHYLESTER MONOHYDROCHLORIDE

Common Name

English

(S)-TYROSINE ETHYL ESTER HYDROCHLORIDE

Systematic Name

English

Code System Code Type Description

ECHA (EC/EINECS)

223-820-2