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Discovery of 1H-pyrazolo[3,4-b]pyrazine derivatives as selective allosteric inhibitor of protein tyrosine phosphatase SHP2 for the treatment of KRASG12C-mutant non-small cell lung cancer
Journal of Biomolecular Structure and Dynamics ( IF 2.7 ) Pub Date : 2024-01-23 , DOI: 10.1080/07391102.2024.2308771 Wen-Qiang Xu 1 , Shi-Zhou Qi 1 , Ji-Feng Zhao 2 , Li-Peng Li 3 , Chuan-Hua Ding 2 , Wen-Shan Liu 2, 4
Journal of Biomolecular Structure and Dynamics ( IF 2.7 ) Pub Date : 2024-01-23 , DOI: 10.1080/07391102.2024.2308771 Wen-Qiang Xu 1 , Shi-Zhou Qi 1 , Ji-Feng Zhao 2 , Li-Peng Li 3 , Chuan-Hua Ding 2 , Wen-Shan Liu 2, 4
Affiliation
The high expression or mutation of SHP2 can induce cancer, so targeting SHP2 has become a new strategy for cancer treatment. In this study, we used the previously reported SHP2 allosteric inhibitor...
中文翻译:
发现 1H-吡唑并[3,4-b]吡嗪衍生物作为蛋白酪氨酸磷酸酶 SHP2 的选择性变构抑制剂,用于治疗 KRASG12C 突变型非小细胞肺癌
SHP2的高表达或突变可诱发癌症,因此靶向SHP2已成为癌症治疗的新策略。在这项研究中,我们使用了之前报道的 SHP2 变构抑制剂......
更新日期:2024-01-23
中文翻译:
发现 1H-吡唑并[3,4-b]吡嗪衍生物作为蛋白酪氨酸磷酸酶 SHP2 的选择性变构抑制剂,用于治疗 KRASG12C 突变型非小细胞肺癌
SHP2的高表达或突变可诱发癌症,因此靶向SHP2已成为癌症治疗的新策略。在这项研究中,我们使用了之前报道的 SHP2 变构抑制剂......