INHIBITORS OF CRL4 UBIQUITIN LIGASE AND USES THEREOF
申请人:Cornell University
公开号:US20150196546A1
公开(公告)日:2015-07-16
The invention is directed to a method of treating a cancer in an animal and a method of increasing DNA repair activity in an animal. The methods comprise administering to an animal in need thereof an effective amount of a small molecule substance that interferes with the activity of CUL4A, such as a 1,3-benzoxathiol-2-one compound, a pyridine thione compound, a 2,6-diamino-4-thiopyran-3,5-dicarbonitrile compound, or a 1,2,4-triazole-3-thiol compound.
Inhibitors of CRL4 ubiquitin ligase and uses thereof
申请人:Cornell University
公开号:US10617683B2
公开(公告)日:2020-04-14
The invention is directed to a method of treating a cancer in an animal and a method of increasing DNA repair activity in an animal. The methods comprise administering to an animal in need thereof an effective amount of a small molecule substance that interferes with the activity of CUL4A, such as a 1,3-benzoxathiol-2-one compound, a pyridine thione compound, a 2,6-diamino-4-thiopyran-3,5-dicarbonitrile compound, or a 1,2,4-triazole-3-thiol compound.
本发明涉及一种治疗动物癌症的方法和一种提高动物 DNA 修复活性的方法。这些方法包括向有需要的动物施用有效量的干扰CUL4A活性的小分子物质,如1,3-苯并氧硫醇-2-酮化合物、吡啶硫酮化合物、2,6-二氨基-4-噻喃-3,5-二甲腈化合物或1,2,4-三唑-3-硫醇化合物。
[EN] INHIBITORS OF CRL4 UBIQUITIN LIGASE AND USES THEREOF<br/>[FR] INHIBITEURS DE L'UBIQUITINE-LIGASE CRL4 ET SES UTILISATIONS
申请人:UNIV CORNELL
公开号:WO2014031759A2
公开(公告)日:2014-02-27
The invention is directed to a method of treating a cancer in an animal and a method of increasing DNA repair activity in an animal. The methods comprise administering to an animal in need thereof an effective amount of a small molecule substance that interferes with the activity of CUL4A, such as a 1,3-benzoxathiol-2-one compound, a pyridine thione compound, a 2,6-diamino-4-thiopyran-3,5-dicarbonitrile compound, or a 1,2,4-triazole-3-thiol compound.
MWI-promoted preparation of 4<i>H</i>-thiopyran derivatives through one-pot multi-component reactions
One-pot reaction of aromatic aldehydes, cyanothioacetamide and malononitrile undermicrowave irradiation proved to be an efficient way for the synthesis of 2,6-diamino-4-aryl-4H-thiopyran-3,5-dicarbonitriles without any added catalyst.