Search Results - Todsaporn, Duangjai

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  1. 1
    Discovery of Novel EGFR Inhibitor Targeting Wild-Type and Mutant Forms of EGFR: In Silico and In Vitro Study

    Discovery of Novel EGFR Inhibitor Targeting Wild-Type and Mutant Forms of EGFR: In Silico and In Vitro Study by Todsaporn, Duangjai, Zubenko, Alexander, Kartsev, Victor, Aiebchun, Thitinan, Mahalapbutr, Panupong, Petrou, Anthi, Geronikaki, Athina, Divaeva, Liudmila, Chekrisheva, Victoria, Yildiz, Ilkay, Choowongkomon, Kiattawee, Rungrotmongkol, Thanyada

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  2. 2
    Structural dynamics and kinase inhibitory activity of three generations of tyrosine kinase inhibitors against wild-type, L858R/T790M, and L858R/T790M/C797S forms of EGFR

    Structural dynamics and kinase inhibitory activity of three generations of tyrosine kinase inhibitors against wild-type, L858R/T790M, and L858R/T790M/C797S forms of EGFR by Todsaporn, Duangjai, Mahalapbutr, Panupong, Poo-arporn, Rungtiva P., Choowongkomon, Kiattawee, Rungrotmongkol, Thanyada

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  3. 3
    Furopyridine Derivatives as Potent Inhibitors of the Wild Type, L858R/T790M, and L858R/T790M/C797S EGFR

    Furopyridine Derivatives as Potent Inhibitors of the Wild Type, L858R/T790M, and L858R/T790M/C797S EGFR by Todsaporn, Duangjai, Zubenko, Alexander, Kartsev, Victor G., Mahalapbutr, Panupong, Geronikaki, Athina, Sirakanyan, Samvel N., Divaeva, Lyudmila N., Chekrisheva, Victoria, Yildiz, Ilkay, Choowongkomon, Kiattawee, Rungrotmongkol, Thanyada

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  4. 4
    Improvement of the solubility and anticancer activity of 6,8-dibromochrysin by encapsulation into β-cyclodextrin and its derivatives

    Improvement of the solubility and anticancer activity of 6,8-dibromochrysin by encapsulation into β-cyclodextrin and its derivatives by Kerdpol, Khanittha, Oo, Amy, Mahalapbutr, Panupong, Todsaporn, Duangjai, Phumphuang, Siraphatsorn, Chavasiri, Warinthorn, Rungrotmongkol, Thanyada, Hannongbua, Supot

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  5. 5
    Enhancing solubility and stability of piperine using β-cyclodextrin derivatives: computational and experimental investigations

    Enhancing solubility and stability of piperine using β-cyclodextrin derivatives: computational and experimental investigations by Ali, Saba, Saokaew, Phattharapawn, Aman, Aamir, Todsaporn, Duangjai, Sanachai, Kamonpan, Krusong, Kuakarun, Hannongbua, Supot, Wolschann, Peter, Mahalapbutr, Panupong, Rungrotmongkol, Thanyada

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  6. 6
    Discovery of Anilino-1,4-naphthoquinones as Potent EGFR Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Comprehensive Molecular Modeling

    Discovery of Anilino-1,4-naphthoquinones as Potent EGFR Tyrosine Kinase Inhibitors: Synthesis, Biological Evaluation, and Comprehensive Molecular Modeling by Mahalapbutr, Panupong, Leechaisit, Ronnakorn, Thongnum, Anusit, Todsaporn, Duangjai, Prachayasittikul, Veda, Rungrotmongkol, Thanyada, Prachayasittikul, Supaluk, Ruchirawat, Somsak, Prachayasittikul, Virapong, Pingaew, Ratchanok

    Published in ACS omega
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