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DC Field | Value | Language |
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dc.contributor.author | Sakchai Chaibun | en_US |
dc.contributor.author | Wilart Pompimon | en_US |
dc.contributor.author | Chanika Tidchai | en_US |
dc.contributor.author | Noraset Chalaemwongwan | en_US |
dc.contributor.author | Jutarut Wongping | en_US |
dc.contributor.author | Chidawan Kansorn | en_US |
dc.contributor.author | Phansuang Udomputtimekakul | en_US |
dc.contributor.author | Puttinan Meepowpan | en_US |
dc.contributor.author | Siriporn Jungsuttiwong | en_US |
dc.contributor.author | Sarinya Hadsadee | en_US |
dc.contributor.author | Suttiporn Pikulthong | en_US |
dc.contributor.author | Narong Nuntasaen | en_US |
dc.date.accessioned | 2022-10-16T07:24:24Z | - |
dc.date.available | 2022-10-16T07:24:24Z | - |
dc.date.issued | 2021-01-01 | en_US |
dc.identifier.issn | 22103163 | en_US |
dc.identifier.issn | 22103155 | en_US |
dc.identifier.other | 2-s2.0-85120606386 | en_US |
dc.identifier.other | 10.2174/2210315510999200704143606 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120606386&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/77179 | - |
dc.description.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. | en_US |
dc.subject | Medicine | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Chemical composition and biological activities of croton delpyi, croton decalvatus and croton caudatus | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Natural Products Journal | en_US |
article.volume | 11 | en_US |
article.stream.affiliations | Thailand Ministry of Natural Resources and Environment | en_US |
article.stream.affiliations | Ubon Ratchathani University | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Lampang Ra-jabhat University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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