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Details

Stereochemistry ACHIRAL
Molecular Formula C26H24F3N
Molecular Weight 407.4707
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PALIRODEN

SMILES

FC(F)(F)C1=CC(=CC=C1)C2=CCN(CCC3=CC=C(C=C3)C4=CC=CC=C4)CC2

InChI

InChIKey=CNEWKIDCGDXBDE-UHFFFAOYSA-N
InChI=1S/C26H24F3N/c27-26(28,29)25-8-4-7-24(19-25)23-14-17-30(18-15-23)16-13-20-9-11-22(12-10-20)21-5-2-1-3-6-21/h1-12,14,19H,13,15-18H2

HIDE SMILES / InChI

Molecular Formula C26H24F3N
Molecular Weight 407.4707
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Paliroden is an orally active drug that activates the synthesis of endogenous neurotrophins or nerve growth factors. Paliroden was investigated in phase II clinical trial in patients with Alzheimer's disease and to evaluate its effect on 18F-Dopa PET imaging in patients with Parkinson's disease. The further development of paliroden was discontinued due to its insufficient efficacy.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of paliroden (SR57667B) and xaliproden on adult brain neurogenesis.
2006-02

Sample Use Guides

The primary objective is to study the effect of SR57667B (PALIRODEN) at the dose of 4 mg/d on progression of dopaminergic nigro-striatal lesions assessed by 18F-Dopa PET imaging.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:30:35 GMT 2025
Edited
by admin
on Mon Mar 31 18:30:35 GMT 2025
Record UNII
17VJ76L90T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SR5-7667B
Preferred Name English
PALIRODEN
INN  
INN  
Official Name English
paliroden [INN]
Common Name English
SR57667 BASE
Code English
SR57667B
Code English
1-(2-(BIPHENYL-4-YL)ETHYL)-4-(3-(TRIFLUOROMETHYL)PHENYL)-1,2,3,6-TETRAHYDROPYRIDINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C1509
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2107767
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
PRIMARY
DRUG BANK
DB05454
Created by admin on Mon Mar 31 18:30:36 GMT 2025 , Edited by admin on Mon Mar 31 18:30:36 GMT 2025
PRIMARY
SMS_ID
300000034324
Created by admin on Mon Mar 31 18:30:36 GMT 2025 , Edited by admin on Mon Mar 31 18:30:36 GMT 2025
PRIMARY
INN
8638
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
PRIMARY
FDA UNII
17VJ76L90T
Created by admin on Mon Mar 31 18:30:36 GMT 2025 , Edited by admin on Mon Mar 31 18:30:36 GMT 2025
PRIMARY
CAS
188396-77-2
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
PRIMARY
PUBCHEM
11567682
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
PRIMARY
NCI_THESAURUS
C82298
Created by admin on Mon Mar 31 18:30:35 GMT 2025 , Edited by admin on Mon Mar 31 18:30:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID60870180
Created by admin on Mon Mar 31 18:30:36 GMT 2025 , Edited by admin on Mon Mar 31 18:30:36 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET->ACTIVATOR OF EXPRESSION
Related Record Type Details
ACTIVE MOIETY
activates the synthesis of endogenous neurotrophins