Related Experiment Video
Updated: Aug 6, 2026

Curcuminoid-Mediated Antimicrobial Photodynamic Therapy on a Murine Model of Oral Candidiasis
Published on: October 27, 2023
Phaeocaulines H and I, Two New Sesquiterpenoids from Curcuma phaeocaulis with Unprecedented Skeletons and
Fei Liu1,2, Guang-Xu Wu1,2, Xin-Yu Wu3
1Sichuan Provincial Key Laboratory of Lnnovation and Effective Uses of Chinese Medicine Germplasm Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Abstract:
Sesquiterpenoids are a highly diverse group of natural compounds, known for their wide range of biological effects. Among them, the derivatives in the genus Curcuma have garnered significant interest for their intricate structures and potential pharmacological benefits. Curcuma phaeocaulis Val. (Peng Ezhu), a geo-authentic medicinal plant native to Sichuan Province, has been traditionally employed to enhance blood circulation and relieve pain. This study reports the isolation of two new sesquiterpenoids, phaeocauline H (1) and phaeocauline I (2), from C. phaeocaulis rhizomes. Compound 1 exhibits a novel dicyclo[4.3.1]-decane structure, whereas compound 2 contains an uncommon 5/7-fused bicyclic ring system. Detailed spectroscopic analyses and ECD data were employed to ascertain their structures, including absolute configurations. Plausible biosynthetic pathways for both compounds are proposed. Preliminary bioactivity evaluation revealed that both compounds exhibit antiangiogenic activity by preventing the proliferation of HUVECs induced by VEGF.
More Related Videos
10:01Structure-Guided Design and Development of Novel Cyclophilin A Inhibitors and Ganoderiol-F Derivatives: An In-Silico Approach
Published on: June 23, 2026
09:20Preclinical Assessment of the Bioactivity of the Anticancer Coumarin OT48 by Spheroids, Colony Formation Assays, and Zebrafish Xenografts
Published on: June 26, 2018
Related Concept Videos
Inhibition of Cdk Activity
Drugs that Stabilize Microtubules