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
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
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| BIOSYNTHESIS OF L-TYROSINE O-SULPHATE FROM THE METHYL AND ETHYL ESTERS OF L-TYROSINE. | 1965 Feb |
|
| Approaches to the synthesis of some tyrosine-derived marine sponge metabolites: synthesis of verongamine and purealidin N. | 2001 May 4 |
|
| Synthesis of 2-[18F]fluoro-L-tyrosine via regiospecific fluoro-de-stannylation. | 2002 Aug |
|
| Light-driven tyrosine radical formation in a ruthenium-tyrosine complex attached to nanoparticle TiO2. | 2002 Dec 2 |
|
| Synthesis of gossypol atropisomers and derivatives and evaluation of their anti-proliferative and anti-oxidant activity. | 2005 Jul 1 |
|
| Singlet molecular oxygen [O2(1Deltag)]-mediated photodegradation of tyrosine derivatives in the presence of cationic and neutral micellar systems. | 2008 Jun |
|
| Probing molecular motion by double-quantum (13C,13C) solid-state NMR spectroscopy: application to ubiquitin. | 2010 Jan 13 |
|
| High level production of bioactive di- and tri-tyrosine peptides by protease-catalyzed reactions. | 2010 Nov |
|
| Mechanism of papain-catalyzed synthesis of oligo-tyrosine peptides. | 2015 Jul-Aug |
|
| A thermodynamically consistent phase diagram of a trimorphic pharmaceutical, l-tyrosine ethyl ester, based on limited experimental data. | 2018 Sep 26 |
Sample Use Guides
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
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
223-820-2
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY | |||
|
CHEMBL292389
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY | |||
|
FAP58DAZ1E
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY | |||
|
4089-07-0
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY | |||
|
2724939
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY | |||
|
17141
Created by
admin on Sat Dec 16 05:50:55 GMT 2023 , Edited by admin on Sat Dec 16 05:50:55 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
