Honokiol as an α-glucosidase inhibitor DOI Creative Commons

Hua Zhu,

Xin Zhong

Frontiers in Pharmacology, Journal Year: 2024, Volume and Issue: 15

Published: June 19, 2024

Honokiol, a naturally occurring compound from Magnolia obovata Thunb ., has many biological activities, but its anti-α-glucosidase activity is still unclear. Therefore, we determined inhibitory effects against α-glucosidase. Activity assays showed that honokiol was reversible mixed-type inhibitor of α-glucosidase, and IC 50 value 317.11 ± 12.86 μM. Fluorescence results indicated the binding to α-glucosidase caused reduction in activity. 3D fluorescence CD spectra conformational change Docking simulated detailed interactions between including hydrogen hydrophobic bonds. All findings could be used as natural develop agents.

Language: Английский

Safety Evaluation of Curcumol by a Repeated Dose 28-Day Oral Exposure Toxicity Study in Rats DOI Creative Commons

Zhaoxu Yang,

Sheng Wang,

Yawen Hong

et al.

Toxics, Journal Year: 2023, Volume and Issue: 11(2), P. 114 - 114

Published: Jan. 24, 2023

Curcumol, a natural product isolated from the traditional Chinese medicine Rhizoma curcumae, possesses various potential therapeutic values in many diseases. However, evidence of its toxicological profile is currently lacking. In this study, repeated toxicity study curcumol was conducted for first time. SD rats were exposed to doses 250, 500, 1000 mg/kg selected dose formulation 28 days through oral administration. The toxic effects on blood system observed and further validated vivo vitro. Moreover, other hematology biochemistry parameters as well weight organs altered, but no related histopathological signs observed, indicating these changes not regarded toxicologically relevant. Our current findings provide complete understanding safety curcumol, which may contribute investigational new drug application.

Language: Английский

Citations

5

Curcumae Radix: A Review of Traditional Use, Phytochemistry, Pharmacology, Toxicology and Quality Control DOI
Yuting Niu, Haonan Xu,

Yuying Zhang

et al.

Chemistry & Biodiversity, Journal Year: 2024, Volume and Issue: 21(5)

Published: March 11, 2024

Abstract Curcumae Radix (CuR) is a traditional Chinese medicine that has been used in China for more than 1,000 years. It the efficacy of activating blood and relieving pain, promoting qi depression, clearing heart cooling blood, gallbladder removing jaundice. Based on this, many domestic foreign scholars have conducted systematic studies its chemical composition, pharmacological effects, toxicity quality control. Currently, 250 compounds, mainly including terpenoids curcuminoids, isolated identified from CuR, which activities, antitumor, anti‐inflammatory analgesic, antidepressant, hepatoprotective, hemostatic, hematopoietic, treatment diabetes mellitus. In modern clinical practice, CuR widely tumors, breast hyperplasia, hepatitis, stroke. However, generation application Caryophylli Flos, determination concoction process artifacts, specific Quality Marker, establishment control system are problems need to be solved urgently at present.

Language: Английский

Citations

1

Brominated alkyl promotes a red-emissive probe track lipid droplets in cells and fatty liver DOI
Chunfei Wang, Lei Hu, Jing Yang

et al.

Microchemical Journal, Journal Year: 2024, Volume and Issue: 201, P. 110591 - 110591

Published: April 18, 2024

Language: Английский

Citations

1

Polarity-sensitive fluorescent probe based on coumarin derivatives for imaging lipid droplets and diagnosis of non-alcoholic fatty liver DOI
Zhiyu Wang,

Yi Deng,

Jie Wang

et al.

Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: 1314, P. 138843 - 138843

Published: June 2, 2024

Language: Английский

Citations

1

Honokiol as an α-glucosidase inhibitor DOI Creative Commons

Hua Zhu,

Xin Zhong

Frontiers in Pharmacology, Journal Year: 2024, Volume and Issue: 15

Published: June 19, 2024

Honokiol, a naturally occurring compound from Magnolia obovata Thunb ., has many biological activities, but its anti-α-glucosidase activity is still unclear. Therefore, we determined inhibitory effects against α-glucosidase. Activity assays showed that honokiol was reversible mixed-type inhibitor of α-glucosidase, and IC 50 value 317.11 ± 12.86 μM. Fluorescence results indicated the binding to α-glucosidase caused reduction in activity. 3D fluorescence CD spectra conformational change Docking simulated detailed interactions between including hydrogen hydrophobic bonds. All findings could be used as natural develop agents.

Language: Английский

Citations

1