Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C12H18ClN.ClH |
| Molecular Weight | 248.192 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(CC1=CC=CC=C1)NCCCCl
InChI
InChIKey=IDHNGYVCZUQHFV-UHFFFAOYSA-N
InChI=1S/C12H18ClN.ClH/c1-11(14-9-5-8-13)10-12-6-3-2-4-7-12;/h2-4,6-7,11,14H,5,8-10H2,1H3;1H
DescriptionCurator's Comment: description was created based on several sources, including, http://ec.europa.eu/health/documents/community-register/2000/200003093430/anx_3430_en.pdf
Curator's Comment: description was created based on several sources, including, http://ec.europa.eu/health/documents/community-register/2000/200003093430/anx_3430_en.pdf
Mefenorex or (+/-)N-(3-chloropropyl)-1-methyl-2-phenylethylamine is an N-alkylated analogue of amphetamine. The therapeutic efficacy of mefenorex as an adjunctive support in the treatment of obesity for limited periods of time, as well as its ability to be well tolerated, has been amply demonstrated. Mefenorex is considered to be racemic mixture, no available data regarding enantiospecific pharmacological activity of the compound.
CNS Activity
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Toxicokinetics of amphetamines: metabolism and toxicokinetic data of designer drugs, amphetamine, methamphetamine, and their N-alkyl derivatives. | 2002 Apr |
|
| Precursor medications as a source of methamphetamine and/or amphetamine positive drug testing results. | 2002 May |
|
| Impaired cognition and attention in adults: pharmacological management strategies. | 2007 Feb |
Patents
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29728
Created by
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| Code System | Code | Type | Description | ||
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21776
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100000086166
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CHEMBL2110962
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226-985-9
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m7140
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C000450
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SUB03115MIG
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133749
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6X1N18AU15
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C77848
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5586-87-8
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236179
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ACTIVE MOIETY
SUBSTANCE RECORD
