Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C16H18ClN |
Molecular Weight | 259.774 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](CC1=CC=CC=C1)NCC2=CC=CC=C2Cl
InChI
InChIKey=LRXXRIXDSAEIOR-ZDUSSCGKSA-N
InChI=1S/C16H18ClN/c1-13(11-14-7-3-2-4-8-14)18-12-15-9-5-6-10-16(15)17/h2-10,13,18H,11-12H2,1H3/t13-/m0/s1
Molecular Formula | C16H18ClN |
Molecular Weight | 259.774 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18500382Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/9987865 | https://www.ncbi.nlm.nih.gov/pubmed/9050090
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18500382
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/9987865 | https://www.ncbi.nlm.nih.gov/pubmed/9050090
Clobenzorex is a central stimulant and sympathomimetic used as an anti-obesity drug; an n-substituted amphetamine, which is metabolized to amphethamine. Its actions are like those of dexamphetamine and has been used as a drug of abuse.
CNS Activity
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Amphetamine, clobenzorex, and 4-hydroxyclobenzorex levels following multidose administration of clobenzorex. | 2001 Apr |
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Role of substance P on histamine H(3) antagonist-induced scratching behavior in mice. | 2006 Apr |
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Benfluorex and unexplained valvular heart disease: a case-control study. | 2010 Apr 12 |
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Drugs and dilated cardiomyopathies: A case/noncase study in the French PharmacoVigilance Database. | 2010 Mar |
Patents
Substance Class |
Chemical
Created
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admin
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Edited
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Fri Dec 15 16:00:58 GMT 2023
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Record UNII |
4A5352XI2A
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Record Status |
Validated (UNII)
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WHO-VATC |
QA08AA08
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C29728
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A08AA08
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236-434-4
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CLOBENZOREX
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C000490
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