Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Paptawan Thongdee"'
Autor:
Somjintana Taveepanich, Kampanart Chayajarus, Jutharat Jittimanee, Naruedon Phusri, Paptawan Thongdee, Khemmisara Sawatdee, Pharit Kamsri, Auradee Punkvang, Khomson Suttisintong, Pornpan Pungpo, Wanwisa Suwannaloet, Ruttiya Thongrung, Kanjana Pangjit
Publikováno v:
Heliyon, Vol 10, Iss 19, Pp e38213- (2024)
Background: Iron overload and inflammation are severe conditions that can lead to various chronic diseases. However, the current iron chelator drugs have their limitations. The phytochemical compounds from herbals, such as brazilin, the major active
Externí odkaz:
https://doaj.org/article/4403abe0166949e7b03f5667679b8e4a
Autor:
Bundit Kamsri, Bongkochawan Pakamwong, Paptawan Thongdee, Naruedon Phusi, Pharit Kamsri, Auradee Punkvang, Sombat Ketrat, Patchreenart Saparpakorn, Supa Hannongbua, Jidapa Sangswan, Khomson Suttisintong, Sanya Sureram, Prasat Kittakoop, Poonpilas Hongmanee, Pitak Santanirand, Jiraporn Leanpolchareanchai, Kirsty E. Goudar, James Spencer, Adrian J. Mulholland, Pornpan Pungpo
Publikováno v:
Journal of Chemical Information and Modeling. 63:2707-2718
Autor:
Paptawan Thongdee, Chayanin Hanwarinroj, Bongkochawan Pakamwong, Pharit Kamsri, Auradee Punkvang, Jiraporn Leanpolchareanchai, Sombat Ketrat, Patchreenart Saparpakorn, Supa Hannongbua, Kanchiyaphat Ariyachaokun, Khomson Suttisintong, Sanya Sureram, Prasat Kittakoop, Poonpilas Hongmanee, Pitak Santanirand, Galina V. Mukamolova, Rosemary A. Blood, Yuiko Takebayashi, James Spencer, Adrian J. Mulholland, Pornpan Pungpo
Publikováno v:
Journal of Chemical Information and Modeling. 62:6508-6518
Autor:
Bongkochawan Pakamwong, Paptawan Thongdee, Bundit Kamsri, Naruedon Phusi, Pharit Kamsri, Auradee Punkvang, Sombat Ketrat, Patchreenart Saparpakorn, Supa Hannongbua, Kanchiyaphat Ariyachaokun, Khomson Suttisintong, Sanya Sureram, Prasat Kittakoop, Poonpilas Hongmanee, Pitak Santanirand, James Spencer, Adrian J. Mulholland, Pornpan Pungpo
Publikováno v:
Pakamwong, B, Thongdee, P, Spencer, J, Kamsri, B, Mulholland, A J & Pungpo, P 2022, ' Identification of potent DNA Gyrase inhibitors active against mycobacterium tuberculosis ', Journal of Chemical Information and Modeling, vol. 62, no. 7, pp. 1680-1690 . https://doi.org/10.1021/acs.jcim.1c01390
Mycobacterium tuberculosis DNA gyrase manipulates the DNA topology using controlled breakage and religation of DNA driven by ATP hydrolysis. DNA gyrase has been validated as the enzyme target of fluoroquinolones (FQs), second-line antibiotics used fo
Autor:
Malee Prajuabsuk, Duangkamon Viboonratanasri, Panida Prompinit, Lapporn Vayachuta, Pornpan Pungpo, Paptawan Thongdee
Publikováno v:
Polymer Engineering & Science. 61:2172-2182
Autor:
Chayanin Hanwarinroj, Paptawan Thongdee, Darunee Sukchit, Somjintana Taveepanich, Pharit Kamsri, Auradee Punkvang, Sombat Ketrat, Patchreenart Saparpakorn, Supa Hannongbua, Khomson Suttisintong, Prasat Kittakoop, James Spencer, Adrian J. Mulholland, Pornpan Pungpo
Publikováno v:
Hanwarinroj, C, Thongdee, P, Sukchit, D, Taveepanich, S, Punkvang, A, Kamsri, P, Saparpakorn, P, Ketrat, S K, Hannongbua, S, Suttisintong, K, Kittakoop, P, Spencer, J, Mulholland, A J & Pungpo, P 2022, ' In silico design of novel quinazoline-based compounds as potential Mycobacterium tuberculosis PknB inhibitors through 2D and 3D-QSAR, molecular dynamics simulations combined with pharmacokinetic predictions ', Journal of Molecular Graphics and Modelling, vol. 115, 108231 . https://doi.org/10.1016/j.jmgm.2022.108231
Serine/threonine protein kinase B (PknB) is essential to Mycobacterium tuberculosis (M. tuberculosis) cell division and metabolism and a potential anti-tuberculosis drug target. Here we apply Hologram Quantitative Structure Activity Relationship (HQS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::285b19034deaaebc63ba52c3420cdfe5
https://research-information.bris.ac.uk/ws/files/326367115/R1_Maintext_PknB_Final_submitted.pdf
https://research-information.bris.ac.uk/ws/files/326367115/R1_Maintext_PknB_Final_submitted.pdf
Autor:
Naruedon Phusi, Yuta Hashimoto, Naoki Otsubo, Kyohei Imai, Paptawan Thongdee, Darunee Sukchit, Pharit Kamsri, Auradee Punkvang, Khomson Suttisintong, Pornpan Pungpo, Noriyuki Kurita
Publikováno v:
Computers in Biology and Medicine. 152:106434
2-trans enoyl-acyl carrier protein reductase (InhA) is a promising target for developing novel chemotherapy agents for tuberculosis, and their inhibitory effects on InhA activity were widely investigated by the physicochemical experiments. However, t