Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Tienthong Thongpanchang"'
Autor:
Thidarath Rattanaburee, Chompunud Chompunud Na Ayudhya, Tienthong Thongpanchang, Varomyalin Tipmanee, Potchanapond Graidist
Publikováno v:
Molecules, Vol 28, Iss 21, p 7342 (2023)
This research aimed to determine the target protein and molecular mechanism of trans-(±)-kusunokinin ((±)-KU) derivatives (trans-(±)-ARC and trans-(±)-TTPG-B). Molecular docking was used to predict potential synthesized (±)-KU targets among 22 p
Externí odkaz:
https://doaj.org/article/676cf14276ec455e80768fbe7ba462b3
Autor:
Tanotnon Tanawattanasuntorn, Tienthong Thongpanchang, Thanyada Rungrotmongkol, Chonnikan Hanpaibool, Potchanapond Graidist, Varomyalin Tipmanee
Publikováno v:
ACS Omega, Vol 6, Iss 1, Pp 606-614 (2020)
Externí odkaz:
https://doaj.org/article/50bf860425674b0e90e9595ee35d6675
Autor:
Tanotnon Tanawattanasuntorn, Thidarath Rattanaburee, Tienthong Thongpanchang, Potchanapond Graidist
Publikováno v:
Antioxidants, Vol 11, Iss 12, p 2347 (2022)
Synthetic trans-(±)-kusunokinin ((±)KU), a potential anticancer substance, was revealed to have an inhibitory effect on breast cancer. According to the computational modeling prediction, AKR1B1, an oxidative stress and cancer migration protein, cou
Externí odkaz:
https://doaj.org/article/8d14bdce8fc74a1da60d3a5cde5ba3b8
Autor:
Thidarath Rattanaburee, Patpanat Sermmai, Kornthip Tangthana-umrung, Tienthong Thongpanchang, Potchanapond Graidist
Publikováno v:
Molecules, Vol 27, Iss 23, p 8291 (2022)
This study aimed to investigate the cytotoxicity and anticancer activity of (±)-kusunokinin derivatives ((±)-TTPG-A and (±)-TTPG-B). The cytotoxicity effect was performed on human cancer cells, including breast cancer, cholangiocarcinoma, colon an
Externí odkaz:
https://doaj.org/article/eb957a3555e64bf6bb593c86c586d473
Autor:
Thidarath Rattanaburee, Varomyalin Tipmanee, Aman Tedasen, Tienthong Thongpanchang, Potchanapond Graidist
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 129, Iss , Pp 110361- (2020)
Kusunokinin, a lignan compound, inhibits cancer cell proliferation and induces apoptosis; however, the role of kusunokinin is not fully understood. Here, we aimed to identify a target protein of (−)-kusunokinin and determine the protein levels of i
Externí odkaz:
https://doaj.org/article/9bd6a5a9aa6b4c5eb19bdf4020808a99
Autor:
Thidarath Rattanaburee, Tanotnon Tanawattanasuntorn, Tienthong Thongpanchang, Varomyalin Tipmanee, Potchanapond Graidist
Publikováno v:
Molecules, Vol 26, Iss 15, p 4537 (2021)
Trans-(−)-kusunokinin, an anticancer compound, binds CSF1R with low affinity in breast cancer cells. Therefore, finding an additional possible target of trans-(−)-kusunokinin remains of importance for further development. Here, a computational st
Externí odkaz:
https://doaj.org/article/328a8f3227614b63a9db6c83dba987d7
Autor:
Thidarath Rattanaburee, Tienthong Thongpanchang, Krittaphat Wongma, Aman Tedasen, Yaowapa Sukpondma, Potchanapond Graidist
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 117, Iss , Pp - (2019)
Kusunokinin is a potent lignan compound with a several biological properties including antitrypanosomal and anticancer. In this study, (±)-kusunokinin and its derivative, (±)-bursehernin, were synthesized and investigated for their anticancer activ
Externí odkaz:
https://doaj.org/article/5c5be278006e461cb28bd81b4062a262
Autor:
Saitarn Nithimanon, Patpanat Sermmai, Chawanee Thongpanchang, Siriporn Saepua, Tienthong Thongpanchang
Publikováno v:
Acta Crystallographica Section E Crystallographic Communications. 78:1228-1232
The title compound, NorClAD, C18H23ClO2, a metabolite of an anabolic steroid norchlorotestosterone acetate (NClTA), was successfully synthesized. Its molecular structure was characterized by 1H NMR and 13C NMR spectroscopy and single-crystal X-ray di
Autor:
Tienthong Thongpanchang, Kulvadee Dolsophon, Jakapun Soponpong, Jittra Kornsakulkarn, Chawanee Thongpanchang
Publikováno v:
Synlett. 33:1438-1442
Determination of the absolute configuration of chiral secondary diols by chiral derivatizing agent (CDA) and NMR shift difference is of great challenge due to the complication from the interference of the aromatic anisotropic shielding effect of the
Publikováno v:
European Journal of Organic Chemistry. 26