Chuan-Xi Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Chuan-Xi Wang has a total of 132 co-authors. Here are the top co-authors by number of shared publications:
- Hao Gao
Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University, Guangzhou, China
22 shared publications Guo-Dong Chen
Institute of Traditional Chinese Medicine and Natural Products, College of Pharmacy/State Key Laboratory of Bioactive Molecules and Druggability Assessment/International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, Jinan University
14 shared publicationsDan Hu
13 shared publications- Xin-Sheng Yao
State Key Laboratory of Bioactive Molecules and Druggability Assessment, Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, Jinan University, Guangzhou, 510632, China
12 shared publications Xin-Sheng Yao
Institute of Traditional Chinese Medicine and Natural Products, College of Pharmacy/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research/International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China, Jinan University, Guangzhou, China
9 shared publications- Dan Hu
Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy/State Key Laboratory of Bioactive Molecules and Druggability Assessment/International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Ministry of Education (MOE) of China/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, Jinan University, Guangzhou 510632, China
7 shared publications
Latest Publications
- Open Access
- 2 September 2026
- Published by Elsevier in Acta Pharmaceutica Sinica B
Unraveling stereochemical control mechanisms of neuroactive securinine via isotope-guided spatial transcriptomic strategy
- 2 September 2026
- Published by Elsevier in Acta Pharmaceutica Sinica B
Open AccessUnraveling stereochemical control mechanisms of neuroactive securinine via isotope-guided spatial transcriptomic strategy
- 9 August 2026
- Published by Taylor & Francis in Journal of Asian Natural Products Research
- p. 1-8
Myromopholine A, a new unusual diketomorpholine from Myrothecium gramineum
1. Microorganisms, possess distinctive stereoselective enzymatic systems that enable the synthesis of a diverse array of chiral compounds, which are challenging to produce via traditional chemical ...
- 9 August 2026
- Published by Taylor & Francis in Journal of Asian Natural Products Research
- p. 1-8
Myromopholine A, a new unusual diketomorpholine from Myrothecium gramineum
1. Microorganisms, possess distinctive stereoselective enzymatic systems that enable the synthesis of a diverse array of chiral compounds, which are challenging to produce via traditional chemical ...
- Open Access
- 28 February 2025
- Published by Wiley in Advanced Science
- Vol. 12 (16) , e2417566
Morphology Effect of Puffball Spores on Hemostasis: A Promising Solution for Hemostatic Challenges
Hemostatic materials play a crucial role in wound healing by promoting blood concentration or releasing procoagulant factors. While hydrophilic hemostatic materials are effective, they may cause excessive blood loss and difficulty removing from the wound. Conversely, hydrophobic hemostatic materials avoid these issues but may hinder blood concentration and the release of procoagulant factors due to their water‐repellent nature. This study investigates the hemostatic properties and underlying mechanism of puffball (Bovistella sp.) spores, a traditional hemostatic material. The unique hollow ball‐rod morphology and strong water affinity of puffball spores enable efficient water removal, leading to improved blood clotting without the drawbacks typically associated with hydrophilic hemostatic materials. Further analysis reveals that the nano‐protrusions on the spore surface create a textured hydrophobic surface due to the pinning effect, which prevents adhesion to the wound after clotting. Overall, puffball spores exhibit hemostatic efficacy comparable to the commercial agent QuikClot, with enhanced safety and reduced side effects. Their characteristic morphology, physicochemical properties, and chemical compositions offer inspiration for advancing hemostatic materials and addressing current challenges in wound healing. Additionally, this work provides new perspectives for insight into the pharmacological substance basis of traditional medicine, expanding beyond the conventional component‐focused mentality to a material‐based insight.
- 28 February 2025
- Published by Wiley in Advanced Science
- Vol. 12 (16) , e2417566
Open AccessMorphology Effect of Puffball Spores on Hemostasis: A Promising Solution for Hemostatic Challenges
Hemostatic materials play a crucial role in wound healing by promoting blood concentration or releasing procoagulant factors. While hydrophilic hemostatic materials are effective, they may cause excessive blood loss and difficulty removing from the wound. Conversely, hydrophobic hemostatic materials avoid these issues but may hinder blood concentration and the release of procoagulant factors due to their water‐repellent nature. This study investigates the hemostatic properties and underlying mechanism of puffball (Bovistella sp.) spores, a traditional hemostatic material. The unique hollow ball‐rod morphology and strong water affinity of puffball spores enable efficient water removal, leading to improved blood clotting without the drawbacks typically associated with hydrophilic hemostatic materials. Further analysis reveals that the nano‐protrusions on the spore surface create a textured hydrophobic surface due to the pinning effect, which prevents adhesion to the wound after clotting. Overall, puffball spores exhibit hemostatic efficacy comparable to the commercial agent QuikClot, with enhanced safety and reduced side effects. Their characteristic morphology, physicochemical properties, and chemical compositions offer inspiration for advancing hemostatic materials and addressing current challenges in wound healing. Additionally, this work provides new perspectives for insight into the pharmacological substance basis of traditional medicine, expanding beyond the conventional component‐focused mentality to a material‐based insight.
- 29 July 2023
- Published by Springer Nature in Journal of Natural Medicines
- Vol. 77 (4) , 986-991
Cordythiazole A, the first member of thiazole alkaloids from Chinese cordyceps, with α-glucosidase inhibitory activity
Chinese cordyceps, also known as Dong-Chong-Xia-Cao, is widely recognized as a famous precious tonic herb, and used as traditional Chinese medicine for centuries. It is mainly used for regulating the immune system and improving functions of the lung and kidney, with anti-tumor, anti-inflammatory, and anti-diabetic activities. Due to its rarity and preciousness, a few chemical components are isolated and identified. Moreover, most of them are common chemical components and widely distributed in other natural resources, such as nucleosides, sterols, fatty acids, sugar alcohols, and peptides. Therefore, a large number of active substances of Chinese cordyceps is still unclear. During our search for chemical constituents of Chinese cordyceps, a new thiazole alkaloid, cordythiazole A (1), was isolated and identified. Its structure was elucidated by comprehensive spectroscopic analysis and single-crystal X-ray diffraction analysis. This is the first report of the presence of thiazole alkaloid in Chinese cordyceps, which adds a new class of metabolite of Chinese cordyceps. Furthermore, a putative biosynthesis pathway of cordythiazole A was proposed based on possible biogenic precursor, genes, and literatures. In addition, it showed α-glucosidase inhibitory activity with potency close to that of acarbose. The discovery of cordythiazole A with α-glucosidase inhibitory activity adds a new class of potential anti-diabetes ingredient in Chinese cordyceps. Graphical abstract
- 29 July 2023
- Published by Springer Nature in Journal of Natural Medicines
- Vol. 77 (4) , 986-991
Cordythiazole A, the first member of thiazole alkaloids from Chinese cordyceps, with α-glucosidase inhibitory activity
Chinese cordyceps, also known as Dong-Chong-Xia-Cao, is widely recognized as a famous precious tonic herb, and used as traditional Chinese medicine for centuries. It is mainly used for regulating the immune system and improving functions of the lung and kidney, with anti-tumor, anti-inflammatory, and anti-diabetic activities. Due to its rarity and preciousness, a few chemical components are isolated and identified. Moreover, most of them are common chemical components and widely distributed in other natural resources, such as nucleosides, sterols, fatty acids, sugar alcohols, and peptides. Therefore, a large number of active substances of Chinese cordyceps is still unclear. During our search for chemical constituents of Chinese cordyceps, a new thiazole alkaloid, cordythiazole A (1), was isolated and identified. Its structure was elucidated by comprehensive spectroscopic analysis and single-crystal X-ray diffraction analysis. This is the first report of the presence of thiazole alkaloid in Chinese cordyceps, which adds a new class of metabolite of Chinese cordyceps. Furthermore, a putative biosynthesis pathway of cordythiazole A was proposed based on possible biogenic precursor, genes, and literatures. In addition, it showed α-glucosidase inhibitory activity with potency close to that of acarbose. The discovery of cordythiazole A with α-glucosidase inhibitory activity adds a new class of potential anti-diabetes ingredient in Chinese cordyceps. Graphical abstract
- Open Access
- 21 March 2023
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 13 (9) , 3930-3944
Aureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
- 21 March 2023
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 13 (9) , 3930-3944
Open AccessAureane-type sesquiterpene tetraketides as a novel class of immunomodulators with interleukin-17A inhibitory activity
- Open Access
- 1 February 2021
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 11 (2) , 588-597
A four-protein metabolon assembled by a small peptide protein creates the pentacyclic carbonate ring of aldgamycins
- 1 February 2021
- Published by Elsevier in Acta Pharmaceutica Sinica B
- Vol. 11 (2) , 588-597
Open AccessA four-protein metabolon assembled by a small peptide protein creates the pentacyclic carbonate ring of aldgamycins
- 1 August 2020
- Published by Elsevier in Bioorganic Chemistry
- Vol. 101, 104043
N-methoxy-β-carboline alkaloids with inhibitory activities against Aβ42 aggregation and acetylcholinesterase from the stems of Picrasma quassioides
- 1 August 2020
- Published by Elsevier in Bioorganic Chemistry
- Vol. 101, 104043
N-methoxy-β-carboline alkaloids with inhibitory activities against Aβ42 aggregation and acetylcholinesterase from the stems of Picrasma quassioides
- 1 December 2019
- Published by Elsevier in Chinese Journal of Natural Medicines
- Vol. 17 (12) , 906-911
A pair of new tirucallane triterpenoid epimers from the stems of Picrasma quassioides
- 1 December 2019
- Published by Elsevier in Chinese Journal of Natural Medicines
- Vol. 17 (12) , 906-911
A pair of new tirucallane triterpenoid epimers from the stems of Picrasma quassioides
- 1 November 2019
- Published by Elsevier in Fitoterapia
- Vol. 139, 104375
A new cinnamamide derivative and two new β-carboline alkaloids from the stems of Picrasma quassioides
- 1 November 2019
- Published by Elsevier in Fitoterapia
- Vol. 139, 104375
A new cinnamamide derivative and two new β-carboline alkaloids from the stems of Picrasma quassioides