Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C11H15NO3 |
| Molecular Weight | 209.2417 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)[C@@H](N)CC1=CC=C(O)C=C1
InChI
InChIKey=SBBWEQLNKVHYCX-JTQLQIEISA-N
InChI=1S/C11H15NO3/c1-2-15-11(14)10(12)7-8-3-5-9(13)6-4-8/h3-6,10,13H,2,7,12H2,1H3/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 |
|
| Synthesis of 2-[18F]fluoro-L-tyrosine via regiospecific fluoro-de-stannylation. | 2002 Aug |
|
| Singlet molecular oxygen [O2(1Deltag)]-mediated photodegradation of tyrosine derivatives in the presence of cationic and neutral micellar systems. | 2008 Jun |
|
| 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
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SUBSTANCE RECORD
