| 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
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
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
SUBSTANCE RECORD
