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
[H][C@@]1(CCCCN1)[C@H](C(=O)OC)C2=CC3=CC=CC=C3C=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
Sat Dec 16 11:23:37 UTC 2023
by
admin
on
Sat Dec 16 11:23:37 UTC 2023
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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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-
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WIKIPEDIA |
Designer-drugs-HDMP-28
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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| Code System | Code | Type | Description | ||
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T52Y9T2U0W
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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PRIMARY | |||
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HDMP-28
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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PRIMARY | |||
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HDMP-28
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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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 Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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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 Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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231299-82-4
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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9817261
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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DTXSID201027520
Created by
admin on Sat Dec 16 11:23:37 UTC 2023 , Edited by admin on Sat Dec 16 11:23:37 UTC 2023
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
