Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H12NO3.Na |
| Molecular Weight | 229.2076 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CC(=O)NC(CC1=CC=CC=C1)C([O-])=O
InChI
InChIKey=RBMBEFVVHHNLAR-UHFFFAOYSA-M
InChI=1S/C11H13NO3.Na/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9;/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15);/q;+1/p-1
DescriptionCurator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/7340854
Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/7340854
AFALANINE was developed by Medea Research in Italy and licensed to Pulitzer. Phase III clinical trials of MR 708 were completed by Pulitzer. Antidepressant; Antiparkinsonian; Neuroprotectant; Nootropic, Dopamine receptor agonist, was used to treat Major depressive disorder.
CNS Activity
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Digestive proteolytic activity in the Sunn pest, Eurygaster integriceps. | 2009 |
|
| Genetic algorithms as a tool for capillary electrophoresis method development. | 2002 |
|
| [Isolation and characteristics of immobilized aminoacylase from Streptoverticillium olivoreticuli]. | 2001-03-10 |
Patents
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|---|---|---|---|---|
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
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6Z92N83B5U
Created by
admin on Mon Mar 31 22:02:56 GMT 2025 , Edited by admin on Mon Mar 31 22:02:56 GMT 2025
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PRIMARY | |||
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23686419
Created by
admin on Mon Mar 31 22:02:56 GMT 2025 , Edited by admin on Mon Mar 31 22:02:56 GMT 2025
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74407-30-0
Created by
admin on Mon Mar 31 22:02:56 GMT 2025 , Edited by admin on Mon Mar 31 22:02:56 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD
