Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Athip Maha"'
Autor:
Surang Leelawat, Kawin Leelawat, Thaniya Wannakup, Worawan Saingam, Nanthaphong Khamthong, Fameera Madaka, Athip Maha, Patamaporn Pathompak, Lukman Sueree, Thanapat Songsak
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine, Vol 12, Iss 8, Pp 323-332 (2022)
Objective: To investigate the effects of Δ9-tetrahydrocannabinol, the principal psychoactive compound of Cannabis sativa, and cannabinol, a Δ9-tetrahydrocannabinol degradative product, on human non-small cell lung cancer cells. Methods: Δ9-Tetrahy
Externí odkaz:
https://doaj.org/article/056395876eb84491973b535e5a352a37
Autor:
Surang Leelawat, Kawin Leelawat, Thunyatorn Yimsoo, Thaniya Wunnakup, Chaowalit Monton, Nanthaphong Khamthong, Fameera Madaka, Athip Maha, Thanapat Songsak
Publikováno v:
Evidence-based complementary and alternative medicine : eCAM. 2022
Cholangiocarcinoma (CCA) is a very aggressive tumor. The development of a new therapeutic drug for CCA is required. This study aims to evaluate the antitumor effect of ∆9-tetrahydrocannabinol (THC), the major psychoactive component of marijuana (Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2776d99387eb3cec12a00c0fe8164f5b
https://pubmed.ncbi.nlm.nih.gov/36452140
https://pubmed.ncbi.nlm.nih.gov/36452140
Autor:
Surang Leelawat, Kawin Leelawat, Thaniya Wannakup, Worawan Saingam, Nanthaphong Khamthong, Fameera Madaka, Athip Maha, Patamaporn Pathompak, Lukman Sueree, Thanapat Songsak
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine; Aug2022, Vol. 12 Issue 8, p323-332, 10p
Autor:
Souwalak Phongpaichit, Sita Preedanon, Saowanit Saithong, Athip Maha, Patima Phainuphong, Jariya Sakayaroj, Vatcharin Rukachaisirikul, Siriporn Jungsuttiwong, Sarinya Hadsadee
Publikováno v:
Tetrahedron. 74:5659-5664
Three new blennolide derivatives, blennolides L-N (1–3), together with five known metabolites were isolated from the soil-derived fungus Trichoderma asperellum PSU-PSF14. Their structures were determined by analysis of spectroscopic data. Their rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ca39ce959329ccda51ef30a0a615d8a
https://doi.org/10.1016/j.tet.2018.07.041
https://doi.org/10.1016/j.tet.2018.07.041
Autor:
Vatcharin Rukachaisirikul, Jariya Sakayaroj, Sita Preedanon, Souwalak Phongpaichit, Athip Maha
Publikováno v:
Tetrahedron. 73:4597-4601
Six new compounds including four tyrosine derivatives (1–4), and two hydantoin derivatives (5–6) were obtained from the investigation of the endophytic fungus Phoma herbarum PSU-H256, which was isolated from a leaf of Hevea brasiliensis. Their st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3e177de4a6dcd87f12036b58cca138a
https://doi.org/10.1016/j.tet.2017.06.025
https://doi.org/10.1016/j.tet.2017.06.025
Autor:
Vatcharin Rukachaisirikul, Wimarak Poonsuwan, Jariya Sakayaroj, Souwalak Phongpaichit, Athip Maha
Publikováno v:
Tetrahedron. 72:2874-2879
Five new compounds including three dimeric chromanones ( 1 – 3 ), one cyclohexenone ( 4 ) and one benzamide ( 5 ), together with four known metabolites, were isolated from the endophytic fungus Xylaria sp. PSU-H182. Their structures were determined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06f8f72a133a7f69e3840e71150979d8
https://doi.org/10.1016/j.tet.2016.03.095
https://doi.org/10.1016/j.tet.2016.03.095
Autor:
Jariya Sakayaroj, Vatcharin Rukachaisirikul, Wimarak Poonsuwan, Patchreenart Saparpakorn, Athip Maha, Supa Hannongbua, Saowanit Saithong, Souwalak Phongpaichit
Publikováno v:
Phytochemistry. 122:223-229
Investigation of the fungus Phoma herbarum PSU-H256 isolated from a leaf of Hevea brasiliensis resulted in the isolation of eight terezine derivatives (E-L) together with four known compounds. Their structures were established by analysis of spectros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad00bc30ed8da24010fce1044e7b5b89
https://doi.org/10.1016/j.phytochem.2015.11.009
https://doi.org/10.1016/j.phytochem.2015.11.009