Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H22N2O2 |
| Molecular Weight | 262.3474 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCCC2=C1C(OCC3CNCCO3)=CC=C2
InChI
InChIKey=VXQWMLATWQSCBE-UHFFFAOYSA-N
InChI=1S/C15H22N2O2/c1-17-8-3-5-12-4-2-6-14(15(12)17)19-11-13-10-16-7-9-18-13/h2,4,6,13,16H,3,5,7-11H2,1H3
| Molecular Formula | C15H22N2O2 |
| Molecular Weight | 262.3474 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Dabelotine is a cognitive-enhancing drug, developed by Servier. The drug has been shown to improve some aspects of cognitive processes, such as attention, curiosity, motivation, acquisition, and recall of memory. Dabelotine has also been shown to reduce the effect of an anticholinergic drug such as scopolamine. The drug increases the in vitro K+-induced norepinephrine release in rodent cerebral slices, and have no effect on noradrenergic and cholinergic receptor binding sites. Dabelotine was investigated in phase 2 clinical trials for the treatment of dementia, where it was demonstrated that 50-mg and 100-mg doses produced an improvement in reaction time and performance in memory tasks.
CNS Activity
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 06:53:49 GMT 2025
by
admin
on
Wed Apr 02 06:53:49 GMT 2025
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| Record UNII |
6RY56RB98P
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| Record Status |
Validated (UNII)
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| Record Version |
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| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C29747
Created by
admin on Wed Apr 02 06:53:49 GMT 2025 , Edited by admin on Wed Apr 02 06:53:49 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C74103
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SUB06881MIG
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6RY56RB98P
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118976-38-8
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100000083971
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CHEMBL2106098
Created by
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177949
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DTXSID70869621
Created by
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7289
Created by
admin on Wed Apr 02 06:53:49 GMT 2025 , Edited by admin on Wed Apr 02 06:53:49 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |