Related Experiment Video
Updated: Aug 5, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Lathyrane Diterpenoids: Half-Century of Chemical Insights and Therapeutic Potential
Diego Caprioglio1, Daniela Imperio2, Alberto Minassi1
1Department of Pharmaceutical Science, University of Piemonte Orientale, Via Bovio 6, 28100 Novara, Italy.
Abstract:
Despite being discovered over a century ago, lathyrane diterpenoids have only recently attracted significant attention from the organic chemistry community due to their distinctive carbon framework, characterized by a 5/11/3 tricyclic system. The conformational rigidity of these scaffolds promotes close spatial proximity between functional groups, making transannular reactions a powerful tool for the construction of new complex polycyclic architectures. In parallel, compounds from the genus Euphorbia have emerged as versatile molecular frameworks in medicinal chemistry, exhibiting a wide range of biological activities, including cytotoxic, antiviral, and neuroprotective effects. This review summarizes recent advances in the field, with particular emphasis on synthetic strategies, structural diversity, and medicinal chemistry aspects of this intriguing class of secondary metabolites.
Related Concept Videos
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Drug Discovery: Overview
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
Targets for Drug Action: Overview
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of the aromatic...
