Details
| Stereochemistry | MIXED |
| Molecular Formula | C15H21N.ClH |
| Molecular Weight | 251.795 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCNC1C2CCC(C2)C1C3=CC=CC=C3
InChI
InChIKey=CVFSMSTXULJISA-UHFFFAOYSA-N
InChI=1S/C15H21N.ClH/c1-2-16-15-13-9-8-12(10-13)14(15)11-6-4-3-5-7-11;/h3-7,12-16H,2,8-10H2,1H3;1H
| Molecular Formula | C15H21N |
| Molecular Weight | 215.3339 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Fencamfamin is a camphane derivative, although lacking typical sympathomimetic properties. It is structurally related to the phenylethylamines. It is a central nervous stimulant with pharmacological properties similar to amphetamine. Fencamfamin developed primarily as appetite suppressant or pscyhostimulant, not to increase awareness. Fencamfamin reduces REM sleep and prevents fatigue in subjects deprived of sleep. Fencamfamin raises a mood.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:15:21 GMT 2025
by
admin
on
Mon Mar 31 18:15:21 GMT 2025
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| Record UNII |
0M1J60BWEX
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C66884
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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CHEMBL7010
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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SUB02110MIG
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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2240-14-4
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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172254
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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DBSALT000814
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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DTXSID70945050
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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C76051
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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102773
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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218-805-2
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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C020900
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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0M1J60BWEX
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY | |||
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100000087502
Created by
admin on Mon Mar 31 18:15:21 GMT 2025 , Edited by admin on Mon Mar 31 18:15:21 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
