Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H19N |
| Molecular Weight | 225.3288 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC(CC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=IGFZMQXEKIZPDR-UHFFFAOYSA-N
InChI=1S/C16H19N/c1-2-17-16(15-11-7-4-8-12-15)13-14-9-5-3-6-10-14/h3-12,16-17H,2,13H2,1H3
| Molecular Formula | C16H19N |
| Molecular Weight | 225.3288 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:41:42 UTC 2023
by
admin
on
Sat Dec 16 10:41:42 UTC 2023
|
| Record UNII |
NG69VG2948
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
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| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-Ephenidine
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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SUB179336
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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NG69VG2948
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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110821
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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60951-19-1
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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100000164749
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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DTXSID601032416
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
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PRIMARY | |||
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EPHENIDINE
Created by
admin on Sat Dec 16 10:41:42 UTC 2023 , Edited by admin on Sat Dec 16 10:41:42 UTC 2023
|
PRIMARY | Ephenidine (also known as NEDPA and EPE) is a dissociative anesthetic that has been sold online as a designer drug.[1][2] It is illegal in some countries as a structural isomer of the banned opioid drug lefetamine, but has been sold in countries where it is not yet banned. Ephenidine and related diarylethylamines have been studied in vitro as treatments for neurotoxic injuries, and are antagonists of the NMDA receptor. |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
