Abstract:
Un compuesto ácido 3-[5-(2-fluoro-fenil)-[1,2,4]oxadiazol-3-il]-benzoico, que tiene la estructura:**Fórmula** o una sal farmacéuticamente aceptable del mismo.
Abstract:
En la presente se proveen procesos mejorados para la síntesis de derivados de tetrahidro beta-carbolina sustituida. En particular, en la presente se proveen procesos mejorados útiles para la preparación de 6-cloro-1-(4-metoxifenil)-3,4-dihidro 1 H-pirido[3,4-b]indol-2(9H)-carboxilato de (S)-4-clorofenilo. Fórmula (I).
Abstract:
La presente invencion se refiere a metodos, compuestos, y composiciones para tratar o evitar enfermedades relacionadas con mutaciones sin sentido en un ARNm al administrar los compuestos o composiciones de la presente invencion; mas particularmente, la presente invencion se refiere a metodos, compuestos, y composiciones para suprimir la terminacion de la traduccion prematura relacionada con una mutacion si sentido en un ARNm.
Abstract:
The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutation in an mRNA.
Abstract:
The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutation in an mRNA.
Abstract:
Provided herein are improved processes for the synthesis of substituted tetrahydro beta-carboline derivatives. In particular, provided herein are improved processes useful for the preparation of (S)-4-chlorophenyl 6-chloro- 1 -(4-methoxyphenyl)-3,4-dihydro- 1 H-pyrido [3,4-b]indole-2(9H)-carboxylate. Formula (I)
Abstract:
Compounds that selectively inhibit pathological production of human vascular endothelial growth factor (VEGF) and compositions comprising such Compounds are described. Compounds that inhibit viral replication or the production of viral RNA or DNA or viral protein and compositions comprising such Compounds are described. Also described are methods of reducing VEGF using such Compounds and methods for treating cancer and non-neoplastic conditions involving the administration of such Compounds. Further described are methods of inhibiting viral replications or the production of viral RNA or DNA or viral protein using such Compounds and methods for treating viral infections involving the administration of such Compounds. The Compounds may be administered as a single agent therapy or in combination with one ore more additional therapies to a human in need of such treatment.
Abstract:
The present invention relates to methods, compounds, and compositions for treating or preventing diseases associated with nonsense mutations in an mRNA by administering the compounds or compositions of the present invention. More particularly, the present invention relates to methods, compounds, and compositions for suppressing premature translation termination associated with a nonsense mutation in an mRNA.