Related Experiment Video
Updated: Jan 15, 2026

Analysis of Raw and Processed Cyperi Rhizoma Samples Using Liquid Chromatography-Tandem Mass Spectrometry in Rats with Primary Dysmenorrhea
Published on: December 23, 2022
Terpenoid Compounds From Montanoa tomentosa Cerv. With Anti-inflammatory Potential
Eric Jaziel Medrano-Sánchez1, Ammy Joana Gallegos-García2, Ricardo López-Rodríguez1
1División Académica de Ciencias Básicas, Universidad Juárez Autónoma De Tabasco, Cunduacan, Mexico.
Abstract:
Montanoa tomentosa has been used in Mexican traditional medicine as a labor inducer and contraceptive, as well as for the treatment of pain after childbirth. In this sense, M. tomentosa is an important source of metabolites with potent anti-inflammatory activity. The objective of this work was to evaluate the anti-inflammatory activity of extracts: n-hexane (MtHex), ethyl acetate (MtAc), and methanol (MtMe), and compounds isolated from leaves of M. tomentosa. The anti-inflammatory effect was evaluated in the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced ear edema model in mice. The compounds were structurally characterized using one- and two-dimensional nuclear magnetic resonance spectroscopy. The MtHex (1 mg/ear) reduced edema (61.16 ± 3.8%), showing a similar effect to indomethacin (70.02 ± 1.24%). From the MtHex extract, the following compounds were isolated and identified: β-sitosterol (1), stigmasterol (2), kaurenoic acid (3), grandiflorenic acid (4), taraxasterol (5), and 15-cinnamoylkaurenic acid (6). Compounds 5, 6, and the mixture of 3 and 4 were evaluated; compound 6 showed the most significant effect in the TPA model (79.05 ± 3.07%). These exploratory results demonstrate that M. tomentosa could be an important source of terpene-type metabolites such as kaurenoic acid derivatives and sterols with potential anti-inflammatory effects.
More Related Videos
Related Concept Videos
Chemotherapy-Induced Nausea and Vomiting: Cannabinoids
Two synthetic agonists of THC,...
Antiasthma Drugs: Muscarinic Receptor Antagonists
Antimuscarinic agents compete with ACh for the same binding site on the muscarinic receptors. By binding to these receptors, they inhibit the downstream effects of ACh and block the parasympathetic...
Cholinergic Antagonists: Therapeutic Uses
Respiratory Tract: Ipratropium, aclidinium, and tiotropium treat asthma, chronic bronchitis, and chronic obstructive pulmonary disease (COPD). They protect against bronchoconstriction caused by irritants like cigarette smoke, sulfur dioxide, and ozone. They also help reduce nasopharyngeal...
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...
Aromatic Compounds: Overview
In 1825, Faraday isolated...

