Related Experiment Video
Updated: Jul 17, 2026

Transient Expression in Nicotiana Benthamiana Leaves for Triterpene Production at a Preparative Scale
Published on: August 16, 2018
New Polyene Pregnane Steroids From the Stems of Nerium oleander: Structural Characterization and In Vitro
Tong-Xin Zheng1, Zi-Xin Lin1, He-Hui Zhan1
1Guangdong Engineering Technology Research Center for the Development and Utilization of Mangrove Wetland Medicinal Resources, School of Ocean and Tropical Medicine, Guangdong Medical University, Zhanjiang, P.R. China.
None:
Phytochemical investigation on the stems of Nerium oleander led to the isolation of four previously undescribed polyene pregnane steroids, namely neristerone A-D (1-4), together with six known analogues (5-10). Their structures were fully elucidated by extensive spectroscopic analysis (UV, IR, HR-ESI-MS, and NMR) and electronic circular dichroism (ECD) calculations. All isolates were evaluated for the inhibitory effects on nitric oxide (NO) production in lipopolysaccharide (LPS)-induced RAW264.7 macrophages. Notably, compounds 1, 4, and 10 exhibited significant inhibitory activity with IC50 values ranging from 11.27 ± 0.81 to 18.13 ± 1.25 µmol/L, which were lower than that of the positive control dexamethasone (21.48 ± 0.83 µmol/L). A preliminary structure-activity relationship analysis was also discussed. This study expands the chemical diversity of polyene pregnane steroids from N. oleander and provides new insights into their anti‑inflammatory potency.
More Related Videos
07:36Analysis of Raw and Processed Cyperi Rhizoma Samples Using Liquid Chromatography-Tandem Mass Spectrometry in Rats with Primary Dysmenorrhea
Published on: December 23, 2022
07:59A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Related Concept Videos
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Polymer Classification: Stereospecificity
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
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...