1-Pentyl-3-(2-methoxybenzoyl)indole

From WikiMD's Wellness Encyclopedia


1-Pentyl-3-(2-methoxybenzoyl)indole is a synthetic cannabinoid that belongs to the indole family of compounds. It is often used in scientific research to study the effects of cannabinoids on the human body. This compound is structurally related to other synthetic cannabinoids that have been used in the formulation of designer drugs.

Chemical Structure and Properties[edit | edit source]

1-Pentyl-3-(2-methoxybenzoyl)indole is characterized by its indole core, which is a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The compound has a pentyl chain attached to the nitrogen atom of the indole, and a 2-methoxybenzoyl group attached to the third position of the indole ring.

Molecular Formula[edit | edit source]

The molecular formula of 1-Pentyl-3-(2-methoxybenzoyl)indole is C21H25NO2.

Molecular Weight[edit | edit source]

The molecular weight of this compound is 323.43 g/mol.

Chemical Identifiers[edit | edit source]

  • CAS Number: 155471-08-2
  • PubChem CID: 444693

Pharmacology[edit | edit source]

1-Pentyl-3-(2-methoxybenzoyl)indole acts as an agonist at the cannabinoid receptors, primarily the CB1 and CB2 receptors. These receptors are part of the endocannabinoid system, which plays a role in regulating various physiological processes including pain sensation, mood, and appetite.

Mechanism of Action[edit | edit source]

As a synthetic cannabinoid, 1-Pentyl-3-(2-methoxybenzoyl)indole mimics the action of naturally occurring cannabinoids such as tetrahydrocannabinol (THC), the active component of cannabis. It binds to the cannabinoid receptors in the brain and other parts of the body, leading to altered neurotransmitter release and modulation of synaptic transmission.

Legal Status[edit | edit source]

The legal status of 1-Pentyl-3-(2-methoxybenzoyl)indole varies by country. In many jurisdictions, it is classified as a controlled substance due to its potential for abuse and lack of accepted medical use.

Safety and Toxicology[edit | edit source]

The safety profile of 1-Pentyl-3-(2-methoxybenzoyl)indole is not well-established, and its use is associated with potential adverse effects similar to those of other synthetic cannabinoids. These may include tachycardia, hypertension, anxiety, and hallucinations.

Research Applications[edit | edit source]

This compound is primarily used in research settings to study the effects of synthetic cannabinoids on the central nervous system and to develop potential therapeutic agents targeting the endocannabinoid system.

Also see[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 Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD