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
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
| 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.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT00220272
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
Edited
Mon Mar 31 18:30:35 GMT 2025
by
admin
on
Mon Mar 31 18:30:35 GMT 2025
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| Record UNII |
17VJ76L90T
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C1509
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CHEMBL2107767
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DB05454
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8638
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17VJ76L90T
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11567682
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C82298
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DTXSID60870180
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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TARGET->ACTIVATOR OF EXPRESSION |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
activates the synthesis of endogenous neurotrophins
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