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D-3-phosphoglycerate dehydrogenase allosteric inhibitor and use thereof

机译:D-3-磷酸甘油酸脱氢酶变构抑制剂及其用途

摘要

This application discloses a D-3-phosphoglycerate dehydrogenase allosteric inhibitor and the use thereof. In one class is the benzoyl hydrazine compound for the allosteric site MDL-1 of the enzyme, and the other class is the furan compound for the allosteric site MDL-2 of the enzyme. In vitro enzymatic activity tests, cell viability tests and mouse xenograft model experiments confirm that the two classes of allosteric inhibitors can specifically inhibit the activity of D-3-phosphoglycerate dehydrogenase and delay the growth of cancer cells by reducing the overexpression of the enzyme in cancer cells. Same are used alone or in combination, or in combination with other anti-cancer drugs and can treat, prevent, or inhibit tumor diseases, including breast cancer, colon cancer, melanoma and non-small cell lung cancer.
机译:该申请公开了D-3-磷酸甘油酸脱氢酶变构抑制剂及其用途。一类是用于酶的变构位点MDL-1的苯甲酰肼化合物,另一类是用于酶的变构位点MDL-2的呋喃化合物。体外酶活性测试,细胞活力测试和小鼠异种移植模型实验证实,这两类变构抑制剂可以通过减少癌症中D-3-磷酸甘油酸脱氢酶的过表达来特异性抑制D-3-磷酸甘油酸脱氢酶的活性并延迟癌细胞的生长。细胞。它们可以单独或组合使用,或与其他抗癌药物组合使用,可以治疗,预防或抑制肿瘤疾病,包括乳腺癌,结肠癌,黑色素瘤和非小细胞肺癌。

著录项

  • 公开/公告号US10722489B2

    专利类型

  • 公开/公告日2020-07-28

    原文格式PDF

  • 申请/专利权人 PEKING UNIVERSITY;

    申请/专利号US201916405569

  • 发明设计人 LUHUA LAI;YING LIU;QIAN WANG;PEI LIU;

    申请日2019-05-07

  • 分类号A61K31/15;A61K31/341;A61P35;

  • 国家 US

  • 入库时间 2022-08-21 11:29:20

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