Please use this identifier to cite or link to this item:
http://cmuir.cmu.ac.th/jspui/handle/6653943832/77179
Title: | Chemical composition and biological activities of croton delpyi, croton decalvatus and croton caudatus |
Authors: | Sakchai Chaibun Wilart Pompimon Chanika Tidchai Noraset Chalaemwongwan Jutarut Wongping Chidawan Kansorn Phansuang Udomputtimekakul Puttinan Meepowpan Siriporn Jungsuttiwong Sarinya Hadsadee Suttiporn Pikulthong Narong Nuntasaen |
Authors: | Sakchai Chaibun Wilart Pompimon Chanika Tidchai Noraset Chalaemwongwan Jutarut Wongping Chidawan Kansorn Phansuang Udomputtimekakul Puttinan Meepowpan Siriporn Jungsuttiwong Sarinya Hadsadee Suttiporn Pikulthong Narong Nuntasaen |
Keywords: | Medicine;Pharmacology, Toxicology and Pharmaceutics |
Issue Date: | 1-Jan-2021 |
Abstract: | Background: C. delpyi, C. decalvatus and C. caudatus are in the Euphorbiaceae family. The aerial parts, such as twigs, leaves and barks of these plants are used as traditional medicine such as anti-inflammatory, cytotoxicity, and antifungal properties. Objectives: The aims of this work were 1) to study the chemical composition of C. delpyi, C. decal-vatus, and C. caudatus 2) to test the antibacterial, anti-HIV-1 RT, and cytotoxicity activities of crude extracts and pure compounds from these plants. Methods: Extraction, separation and purification of three plants were performed following chroma-tographic method. The biological activities, including antibacterial, anti-HIV-1 RT and cytotoxicity assay of three plants, were evaluated by the standard methods. Results: Phytochemical investigation of C. delpyi highlighted a new clerodane diterpenoid; cro-tondelpyitin A (1). The five known compounds were found, such as acetyl aleuritolic acid (2), 5-hydroxy-7,4′-dimethoxyflavone (3), and pilloin (4) in C. decalvatus and 3α-benzoyloxy-D while A-friedo-oleanan-27,16α-lactone (5), and bergenin (6) in C. caudatus. Compound 3 showed the most effective antibacterial activities with MIC in range <0.16-1.25 mg/mL, and MBC in range 0.6->5.0 mg/mL. The six compounds were inactive with anti-HIV-1 RT. In addition, compound 4 was active for cytotoxic activities on FaDu and KKU-M213 at <4 µg/mL. Conclusion: The present study reveals that the Croton species are sources of diterpenoid-type compounds and a significant guide for further research of chemical constituents from these plants as potential medicines. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120606386&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/77179 |
ISSN: | 22103163 22103155 |
Appears in Collections: | CMUL: Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.