Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Chayanin, Hanwarinroj"'
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:
Chayanin Hanwarinroj, Nareudon Phusi, Bundit Kamsri, 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, Phusi, N, Kamsri, B, Kamsri, P, Punkvang, A, Ketrat, S, Saparpakorn, P, Hannongbua, S, Suttisintong, K, Kittakoop, P, Spencer, J, Mulholland, A J & Pungpo, P 2022, ' Discovery of novel and potent InhA inhibitors by an in silico screening and pharmacokinetic prediction ', Future Medicinal Chemistry, vol. 14, no. 10, pp. 717-729 . https://doi.org/10.4155/fmc-2021-0348
Aim: In silico screening approaches were performed to discover novel InhA inhibitors. Methods: Candidate InhA inhibitors were obtained from the combination of virtual screening and pharmacokinetic prediction. In addition, molecular mechanics Poisson
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:
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(24)
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:
Chayanin, Hanwarinroj, Nareudon, Phusi, Bundit, Kamsri, Pharit, Kamsri, Auradee, Punkvang, Sombat, Ketrat, Patchreenart, Saparpakorn, Supa, Hannongbua, Khomson, Suttisintong, Prasat, Kittakoop, James, Spencer, Adrian J, Mulholland, Pornpan, Pungpo
Publikováno v:
Future medicinal chemistry. 14(10)
Autor:
Pitak Santanirand, Nitima Suttipanta, Siriluk Rattanabunyong, Poonpilas Hongmanee, Patchreenart Saparpakorn, Pornpan Pungpo, Thimpika Pornprom, Adrian J. Mulholland, Supaporn Seetaha, Khomson Suttisintong, Potjanee Srimanote, Kampanart Chayajarus, Rosemary A. Blood, Naruedon Phusi, Zhaoqiang Chen, Sanya Sureram, Pharit Kamsri, Supa Hannongbua, Philip Hinchliffe, Prasat Kittakoop, Kiattawee Choowongkomon, James Spencer, Yuiko Takebayashi, Chomphunuch Songsiriritthigul, Chayanin Hanwarinroj, Weiliang Zhu, Auradee Punkvang
Publikováno v:
Kamsri, P, Hanwarinroj, C, Phusi, N, Pornprom, T, Chayajarus, K, Punkvang, A, Suttipanta, N, Srimanote, P, Suttisintong, K, Songsiriritthigul, C, Saparpakorn, P, Hannongbua, S, Rattanabunyong, S, Seetaha, S, Choowongkomon, K, Sureram, S, Kittakoop, P, Hongmanee, P, Santanirand, P, Chen, Z, Zhu, W, Blood, R A, Takebayashi, Y, Hinchliffe, P, Mulholland, A J, Spencer, J & Pungpo, P 2020, ' Discovery of New and Potent InhA Inhibitors as Anti-tuberculosis Agents : Structure Based Virtual Screening Validated by Biological Assays and X-ray Crystallography ', Journal of Chemical Information and Modeling, vol. 60 (2020), no. 1, pp. 226-234 . https://doi.org/10.1021/acs.jcim.9b00918
The enoyl-acyl carrier protein reductase InhA of Mycobacterium tuberculosis is an attractive, validated target for antituberculosis drug development. Moreover, direct inhibitors of InhA remain effective against InhA variants with mutations associated
Autor:
Sanya Sureram, Potjanee Srimanote, Nitima Suttipanta, Pharit Kamsri, Khomson Suttisintong, Prasat Kittakoop, Bongkochawan Pakamwong, Pornpan Pungpo, James Spencer, Chomphunuch Songsiriritthigul, Chayanin Hanwarinroj, Auradee Punkvang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72783a1d4e95393c79c790814aac5c86
https://doi.org/10.1002/prot.26268/v2/response1
https://doi.org/10.1002/prot.26268/v2/response1
Autor:
Noriyuki Kurita, Takuya Ezawa, Shogo Tomioka, Bandit Khamsri, Riku Sato, Pornpan Pungpo, Naruedon Phusi, Pharit Kamsri, Auradee Punkvang, Chayanin Hanwarinroj
Publikováno v:
Journal of Molecular Graphics and Modelling. 88:299-308
2-trans enoyl-acyl carrier protein reductase (InhA) has been identified as a promising target for the development of novel chemotherapy for tuberculosis. In the present study, a series of heteroaryl benzamide derivatives were selected as potent inhib