摘要:
Disclosed herein are triazine compounds of formula (I) and methods of making and using thereof to treat malaria, provide chemoprophylaxis, and/or treat or inhibit infection by one or more Plasmodium spp .
摘要:
The present invention relates to 2-amino-4-arylpyrimidine and 2-amino-4-aryltriazine compounds as inhibitors of heat shock protein 90 family of chaperone proteins. The invention also features pharmaceutical compositions and kits that include the compounds and compositions of the invention. The invention further relates to the medical use of these compounds and compositions for the treatment of a disorder in a subject. For example, the disorder is a neurodegenerative disease.
摘要:
and related methods for treating a person having a disorder characterized by undesirable 5-HT2B receptor signaling, such as migraine, irritable bowel syndrome (IBS), pulmonary arterial hypertension (PAH), fibrosis, hepatocellular cancer, a small intestinal neuroendocrine tumor, cardiovascular disorders, and gastrointestinal (GI) tract disorders.
摘要:
The present invention provides substituted 1,3,5-triazine compounds of Formula (I):
wherein X, Y and Z are independently selected from the group consisting of CH and N; wherein m is an integer from 2 to 5; wherein X, Y and Z include at least one CH atom and at least one N atom; and, wherein a N atom may simultaneously occupy only the X and Z positions; R 1 is selected from the group consisting of hydrogen and NH 2 ; and, R 2 is selected from the group consisting of phenyl (wherein phenyl is substituted with one substituent selected from the group consisting of halogen and heterocyclyl) and 1,4-benzodioxinyl; and pharmaceutically acceptable salts thereof as kinase inhibitors and a method for treating or ameliorating a kinase mediated disorder.
摘要翻译:本发明提供式(I)的取代的1,3,5-三嗪化合物:其中X,Y和Z独立地选自CH和N; 其中m是2至5的整数; 其中X,Y和Z包括至少一个CH原子和至少一个N原子; 并且其中N原子可以同时仅占据X和Z位置; R 1选自氢和NH 2; 和R 2选自苯基(其中苯基被一个选自卤素和杂环基的取代基取代)和1,4-苯并二氧杂环己烷基; 和其药学上可接受的盐作为激酶抑制剂和用于治疗或改善激酶介导的病症的方法。
摘要:
The present invention relates to triazinylmethyl sulfonamides of formula (I): wherein T, R 1 , R 2 , R 3 , A, Y and D are as defined in the claims and to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to processes and intermediates for preparing these compounds.
摘要:
The present invention provides substituted 1,3,5-triazine compounds as kinase inhibitors and a method for treating or ameliorating a kinase mediated disorder.