Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Sanya, Sureram"'
Autor:
Natechanok Thipboonchoo, Somsak Fongsupa, Sanya Sureram, Suliporn Sa-nguansak, Chatchai Kesornpun, Prasat Kittakoop, Sunhapas Soodvilai
Publikováno v:
Heliyon, Vol 10, Iss 3, Pp e24983- (2024)
Renal fibrosis is a pathological feature of chronic kidney disease (CKD), progressing toward end-stage kidney disease (ESKD). The aim of this study is to investigate the therapeutic potential of altenusin, a farnesoid X receptor (FXR) agonist derived
Externí odkaz:
https://doaj.org/article/a34a5f2f74874cb3a00e28a2dcc3c7e8
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:
Sanya Sureram, Irene Arduino, Reiko Ueoka, Massimo Rittà, Rachele Francese, Rattanaporn Srivibool, Dhanushka Darshana, Jörn Piel, Somsak Ruchirawat, Luisa Muratori, David Lembo, Prasat Kittakoop, Manuela Donalisio
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 2, p 947 (2022)
Herpesviruses are highly prevalent in the human population, and frequent reactivations occur throughout life. Despite antiviral drugs against herpetic infections, the increasing appearance of drug-resistant viral strains and their adverse effects pro
Externí odkaz:
https://doaj.org/article/f843ee35ddd64829a957adc455b4fbac
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:
Suthat Chottanapund, M.B.M. Van Duursen, Anne Zwartsen, Supatchaya Timtavorn, Panida Navasumrit, Prasat Kittakoop, Sanya Sureram, Mathuros Ruchirawat, Martin Van den Berg
Publikováno v:
Toxicology Reports, Vol 4, Iss , Pp 165-171 (2017)
Naturally occurring depsidones from the marine fungus Aspergillus unguis are known to have substantial anti-cancer activity, but their mechanism of action remains elusive. The purpose of this study was to examine the anti-aromatase activity of two co
Externí odkaz:
https://doaj.org/article/a4ced36dec1b44e1bbd2946be3563b22
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:
Potjanee Srimanote, Pornpan Pungpo, Bongkochawan Pakamwong, Auradee Punkvang, Prasat Kittakoop, James Spencer, Khomson Suttisintong, Chayanin Hanwarinroj, Pharit Kamsri, Nitima Suttipanta, Sanya Sureram, Chomphunuch Songsiriritthigul
Publikováno v:
Songsiriritthigul, C, Hanwarinroj, C, Pakamwong, B, Srimanote, P, Suttipanta, N, Sureram, S, Suttisintong, K, Kamsri, P, Punkvang, A, Spencer, J, Kittakoop, P & Pungpo, P 2021, ' Inhibition of Mycobacterium tuberculosis InhA by 3-nitropropanoic acid ', Proteins: Structure, Function, and Bioinformatics, vol. 90, no. 3, pp. 898-904 . https://doi.org/10.1002/prot.26268
3-Nitropropanoic acid (3NP), a bioactive fungal natural product, was previously demonstrated to inhibit growth of Mycobacterium tuberculosis. Here we demonstrate that 3NP inhibits the 2-trans-enoyl-acyl carrier protein reductase (InhA) from Mycobacte
Autor:
Prasat Kittakoop, Anuchit Phanumartwiwath, Pharit Kamsri, Chatchakorn Eurtivong, Chatchai Kesornpun, Sanya Sureram, Auradee Punkvang, Somsak Ruchirawat, Pornpan Pungpo, Poonpilas Hongmanee
Publikováno v:
Journal of Chemical Research. 45:1003-1015
Isoxazoline derivatives of the natural products eugenol, 1’- S-acetoxychavicol acetate and sclareol are prepared through 1,3-dipolar cycloaddition reactions in an aqueous buffered system. The compounds are evaluated for their antitubercular and ant
Autor:
Hend A. A. Ezelarab, Sanya Sureram, Mohammed A.S. Abourehab, Gamal El-Din A. Abuo-Rahma, Heba A. Hassan, Prasat Kittakoop, M. M. Badr, Samar H. Abbas, Poonpilas Hongmanee
Publikováno v:
Medicinal Chemistry Research. 30:2168-2183
New ciprofloxacin/ quaternary ammonium salts 3a–e were designed and synthesized as potential antimicrobial agents. Most of the prepared derivatives showed promising dual antibacterial/antifungal activities. Compound 3e was the most potent and affor
Autor:
Suthatip Ngokpol, Wittaya Suwakulsiri, Sanya Sureram, Kriengsak Lirdprapamongkol, Thammarat Aree, Suthep Wiyakrutta, Chulabhorn Mahidol, Somsak Ruchirawat, Prasat Kittakoop
Publikováno v:
Marine Drugs, Vol 13, Iss 6, Pp 3567-3580 (2015)
Four new sesquiterpene lactones (3, 4, 6 and 7) and three known compounds, purpuride (1), berkedrimane B (2) and purpuride B (5), were isolated from the marine fungus, Talaromyces minioluteus (Penicillium minioluteum). New compounds were drimane sesq
Externí odkaz:
https://doaj.org/article/b96dcacccc6d4e2f83ed7d0287ea338d