Homo-MDA

From WikiMD.com - Food, Medicine & Wellness Encyclopedia

Chemical compound


Homo-MDA
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 207740-32-1
PubChem 4433
DrugBank
ChemSpider 4278
KEGG


Homo-MDA (3,4-methylenedioxy-N-methylamphetamine) is a psychoactive drug and a member of the amphetamine class of chemicals. It is structurally related to MDMA (3,4-methylenedioxy-N-methylamphetamine) and is known for its stimulant and empathogenic effects.

Chemical Structure and Properties[edit | edit source]

Homo-MDA is a derivative of amphetamine and is characterized by the presence of a methylenedioxy group attached to the phenyl ring. The chemical structure of Homo-MDA is similar to that of MDMA, with the primary difference being the addition of a methylene bridge, which extends the side chain by one carbon atom. This structural modification is responsible for its unique pharmacological properties.

Chemical structure of Homo-MDA

Pharmacology[edit | edit source]

Homo-MDA acts primarily as a serotonin releasing agent, similar to other members of the MDxx class. It increases the levels of serotonin in the synaptic cleft by promoting the release of serotonin from presynaptic neurons. This action is responsible for its mood-enhancing and empathogenic effects. Additionally, Homo-MDA has some affinity for dopamine and norepinephrine transporters, contributing to its stimulant properties.

Effects[edit | edit source]

The effects of Homo-MDA are similar to those of MDMA, including increased energy, enhanced mood, and heightened sensory perception. Users may experience feelings of empathy and emotional closeness, which are characteristic of empathogens. However, the specific effects can vary depending on the dose and individual differences in metabolism and sensitivity.

Legal Status[edit | edit source]

The legal status of Homo-MDA varies by country. In many jurisdictions, it is classified as a controlled substance due to its structural similarity to MDMA and its potential for abuse. It is important for researchers and users to be aware of the legal implications of possessing or distributing Homo-MDA.

Synthesis[edit | edit source]

The synthesis of Homo-MDA involves the use of safrole or isosafrole as starting materials, which are then subjected to a series of chemical reactions to introduce the methylenedioxy group and the extended side chain. The synthesis requires expertise in organic chemistry and access to specialized laboratory equipment.

Related Compounds[edit | edit source]

Homo-MDA is part of a larger family of phenethylamines and amphetamines, which includes compounds such as MDMA, MDA, and MDEA. These compounds share similar chemical structures and pharmacological effects, but differ in their potency and duration of action.

Related Pages[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD