MDMA and Structural analog

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between MDMA and Structural analog

MDMA vs. Structural analog

3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy (E), is a psychoactive drug used primarily as a recreational drug. A structural analog, also known as a chemical analog or simply an analog, is a compound having a structure similar to that of another compound, but differing from it in respect to a certain component.

Similarities between MDMA and Structural analog

MDMA and Structural analog have 3 things in common (in Unionpedia): Amphetamine, Controlled Substances Act, Methamphetamine.

Amphetamine

Amphetamine (contracted from) is a potent central nervous system (CNS) stimulant that is used in the treatment of attention deficit hyperactivity disorder (ADHD), narcolepsy, and obesity.

Amphetamine and MDMA · Amphetamine and Structural analog · See more »

Controlled Substances Act

The Controlled Substances Act (CSA) is the statute establishing federal U.S. drug policy under which the manufacture, importation, possession, use, and distribution of certain substances is regulated.

Controlled Substances Act and MDMA · Controlled Substances Act and Structural analog · See more »

Methamphetamine

Methamphetamine (contracted from) is a potent central nervous system (CNS) stimulant that is mainly used as a recreational drug and less commonly as a second-line treatment for attention deficit hyperactivity disorder and obesity.

MDMA and Methamphetamine · Methamphetamine and Structural analog · See more »

The list above answers the following questions

What MDMA and Structural analog have in common
What are the similarities between MDMA and Structural analog

MDMA and Structural analog Comparison

MDMA has 292 relations, while Structural analog has 25. As they have in common 3, the Jaccard index is 0.95% = 3 / (292 + 25).

References

This article shows the relationship between MDMA and Structural analog. To access each article from which the information was extracted, please visit:

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