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Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation

机译：羟肟酸酯Ar-42的成立衍生物效果抑制I类HDAC酶和癌细胞增殖

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1. Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation [J] . Tng Jiahui, Lim Junxian, Wu Kai-Chen, Journal of Medicinal Chemistry . 2020,第11期

机译：羟肟酸酯Ar-42的成立衍生物效果抑制I类HDAC酶和癌细胞增殖
2. An appraisal of cinnamyl sulfonamide hydroxamate derivatives (HDAC inhibitors) for anti-cancer, anti-angiogenic and anti-metastatic activities in human cancer cells [J] . Reddy Neetinkumar D., Shoja M. H., Biswas Subhankar, Chemico-biological interactions . 2016,第Null期

机译：肉桂酸磺酰胺异羟肟酸酯衍生物（HDAC抑制剂）对人癌细胞中抗癌，抗血管生成和抗转移活性的评估
3. Development of novel β-carboline-based hydroxamate derivatives as HDAC inhibitors with antiproliferative and antimetastatic activities in human cancer cells [J] . Yong Ling, Jing Guo, Qiuxing Yang, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2018,第期

机译：基于新型β-咔啉基的羟肟酸盐衍生物作为HDAC抑制剂，具有人癌细胞中的抗增殖和抗致抗体活性
4. ASPIRIN SWITCHES BIOSYNTHETIC CIRCUITS TRIGGERING NOVEL EICOSANOIDS DURING CELL-CELL INTERACTIONS THAT ARE POTENT INHIBITORS OF NEUTROPHIL MIGRATION AND TUMOR CELL PROLIFERATION [C] . Charles N. Serhan, Joan Claria International Washington Spring Symposium . 1996

机译：阿司匹林在细胞 - 细胞相互作用中触发生物合成电路的生物合成电路在细胞 - 细胞相互作用中触发中性粒细胞迁移和肿瘤细胞增殖的有效抑制剂
5. Selective translocation of cell-impermeable toxins into cancer cells: pHLIP mediated delivery of phallotoxins inhibits cancer proliferation. [D] . Wijesinghe, Dayanjali Diluka. 2011

机译：细胞不可渗透毒素选择性转移到癌细胞中：pHLIP介导的鬼笔毒素传递抑制了癌症的扩散。
6. Thailandepsins are new small molecule class I HDAC inhibitors with potent cytotoxic activity in ovarian cancer cells: a preclinical study of epigenetic ovarian cancer therapy [O] . Andrew J Wilson, Yi-Qiang Cheng, Dineo Khabele 2012

机译：Thaiepsins是新型的小分子I类HDAC抑制剂在卵巢癌细胞中具有强大的细胞毒性活性：表观遗传学卵巢癌治疗的临床前研究
7. Thailandepsins are new small molecule class I HDAC inhibitors with potent cytotoxic activity in ovarian cancer cells: a preclinical study of epigenetic ovarian cancer therapy [O] . Andrew J Wilson, Yi-Qiang Cheng, Dineo Khabele 2012

机译：Thaiepsins是新型的小分子I类HDAC抑制剂，在卵巢癌细胞中具有强大的细胞毒性活性：表观遗传学卵巢癌治疗的临床前研究
8. Chemotherapeutic Potential of G1 Cell Cycle Inhibitor Indole-3-Carbinol and Its More Potent N-Alkoxy Derivatives in Human Breast Cancer Xenografts in Mice [R] . Kerekatte, V. S. , Firestone, G. 2004

机译：G1细胞周期抑制剂吲哚-3-甲醇及其更有效的N-烷氧基衍生物在小鼠人乳腺癌异种移植物中的化疗潜力

Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation

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