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dc.contributor.authorSakchai Chaibunen_US
dc.contributor.authorWilart Pompimonen_US
dc.contributor.authorChanika Tidchaien_US
dc.contributor.authorNoraset Chalaemwongwanen_US
dc.contributor.authorJutarut Wongpingen_US
dc.contributor.authorChidawan Kansornen_US
dc.contributor.authorPhansuang Udomputtimekakulen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.contributor.authorSiriporn Jungsuttiwongen_US
dc.contributor.authorSarinya Hadsadeeen_US
dc.contributor.authorSuttiporn Pikulthongen_US
dc.contributor.authorNarong Nuntasaenen_US
dc.date.accessioned2022-10-16T07:24:24Z-
dc.date.available2022-10-16T07:24:24Z-
dc.date.issued2021-01-01en_US
dc.identifier.issn22103163en_US
dc.identifier.issn22103155en_US
dc.identifier.other2-s2.0-85120606386en_US
dc.identifier.other10.2174/2210315510999200704143606en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120606386&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77179-
dc.description.abstractBackground: 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.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleChemical composition and biological activities of croton delpyi, croton decalvatus and croton caudatusen_US
dc.typeJournalen_US
article.title.sourcetitleNatural Products Journalen_US
article.volume11en_US
article.stream.affiliationsThailand Ministry of Natural Resources and Environmenten_US
article.stream.affiliationsUbon Ratchathani Universityen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsLampang Ra-jabhat Universityen_US
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