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Details

Stereochemistry RACEMIC
Molecular Formula C11H13NO3
Molecular Weight 207.2258
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AFALANINE

SMILES

CC(=O)NC(CC1=CC=CC=C1)C(O)=O

InChI

InChIKey=CBQJSKKFNMDLON-UHFFFAOYSA-N
InChI=1S/C11H13NO3/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)

HIDE SMILES / InChI

Description
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.

Originator

Curator's Comment: AFALANINE was developed by Medea Research in Italy and licensed to Pulitzer.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
[Isolation and characteristics of immobilized aminoacylase from Streptoverticillium olivoreticuli].
2001 Jan-Feb
Genetic algorithms as a tool for capillary electrophoresis method development.
2002
Digestive proteolytic activity in the Sunn pest, Eurygaster integriceps.
2009
Patents

Sample Use Guides

Dogs/rats - AFALANINE (MR-708) produced a mild and transienth hypertension when given to narcotized dogs at the dosage rate of 4.5 mg/kg, and to rats narcotized by bilateral vagotomy at the dosage rate of 5 mg/kg
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
AFALANINE
INN  
INN  
Official Name English
NSC-43242
Code English
N-ACETYL-3-PHENYL-DL-ALANINE
Systematic Name English
afalanine [INN]
Common Name English
N-ACETYLPHENYLALANINE, (±)-
Systematic Name English
N-ACETYLPHENYLALANINE, DL-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
NCI_THESAURUS C73539
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
Code System Code Type Description
CHEBI
21626
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
EVMPD
SUB05280MIG
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
PUBCHEM
2000
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
NCI_THESAURUS
C72682
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
NSC
43242
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
CAS
2901-75-9
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
SMS_ID
100000087706
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
FDA UNII
FFW2NGO18S
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID3045697
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL134570
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
ECHA (EC/EINECS)
220-793-9
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY
INN
6575
Created by admin on Fri Dec 15 16:02:38 GMT 2023 , Edited by admin on Fri Dec 15 16:02:38 GMT 2023
PRIMARY