Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H21NO2 |
| Molecular Weight | 283.3648 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]([C@H]1CCCCN1)C2=CC=C3C=CC=CC3=C2
InChI
InChIKey=DNRNSIJBSCBESJ-IAGOWNOFSA-N
InChI=1S/C18H21NO2/c1-21-18(20)17(16-8-4-5-11-19-16)15-10-9-13-6-2-3-7-14(13)12-15/h2-3,6-7,9-10,12,16-17,19H,4-5,8,11H2,1H3/t16-,17-/m1/s1
| Molecular Formula | C18H21NO2 |
| Molecular Weight | 283.3648 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:23:43 GMT 2025
by
admin
on
Tue Apr 01 16:23:43 GMT 2025
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| Record UNII |
T52Y9T2U0W
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| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Common 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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Systematic Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
Designer-drugs-HDMP-28
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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| Code System | Code | Type | Description | ||
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T52Y9T2U0W
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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PRIMARY | |||
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HDMP-28
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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PRIMARY | |||
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HDMP-28
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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PRIMARY | HDMP-28 or methylnaphthidate is a piperidine based stimulant drug, closely related to methylphenidate, but with the benzene ring replaced by naphthalene. It is a potent dopamine reuptake inhibitor, with several times the potency of methylphenidate and a short duration of action, and is a structural isomer of another potent dopamine reuptake inhibitor, N,O-Dimethyl-4-(2-naphthyl)piperidine-3-carboxylate. | ||
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METHYLNAPHTHIDATE
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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PRIMARY | HDMP-28 is a methylphenidate (ritalin, concerta) analogue which replaces the phenyl moiety with a naphthyl moiety. The modification confers a theoretical increase in SERT affinity, making effects closer to cocaine, and also theoretically gives increased potency over methylphenidate. Despite being known about in scientific literature for many years, HDMP-28 is unusual in that it did not come to market until 2014. This is in stark contrast to many other known recreational drug analogues which were primarily surrected from the literature between 2010-2013. | ||
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1607459-83-5
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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NON-SPECIFIC STEREOCHEMISTRY | |||
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231299-82-4
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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9817261
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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DTXSID201027520
Created by
admin on Tue Apr 01 16:23:43 GMT 2025 , Edited by admin on Tue Apr 01 16:23:43 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
