Patent classifications
C07D515/20
SPIRO-SULFONIMIDAMIDE DERIVATIVES AS INHIBITORS OF MYELOID CELL LEUKEMIA-1 (MCL-1) PROTEIN
The disclosure is directed to compounds of Formula (I). Pharmaceutical compositions comprising compounds of Formula (I) as well as methods of their use and preparation, are also described.
##STR00001##
COMPOUNDS THAT INHIBIT MCL-1 PROTEIN
- Sean P BROWN ,
- David Karl BEDKE ,
- Michael R. DeGraffenreid ,
- Jiasheng Fu ,
- Zhinghong LI ,
- Felix Gonzalez Lopez De Turiso ,
- Ana Gonzalez Buenrostro ,
- Michael W. GRIBBLE JR. ,
- Michael G. Johnson ,
- Todd J. KOHN ,
- Kexue LI ,
- Yunxiao LI ,
- Mike Elias Lizarzaburu ,
- Yosup Rew ,
- Joshua TAYGERLY ,
- Yingcai Wang ,
- Xuelei Yan ,
- Ming Yu ,
- Jiang Zhu ,
- Manuel Zancanella ,
- Xian Yun Jiao ,
- Liusheng Zhu ,
- Xianghong Wang ,
- Julio C. Medina ,
- Jason A. Duquette ,
- Jonathan B. HOUZE ,
- Marc VIMOLRATANA ,
- Mario G. Cardozo ,
- Alan C. Cheng
Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I,
##STR00001##
and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.
Macrocyclic spiroethers as Mcl-1 inhibitors
Provided are compounds represented by Formula (I-A) and the pharmaceutically acceptable salts and solvates thereof, wherein R.sup.8, R.sup.9a, R.sup.9b, R.sup.9c, R.sup.9d, X, Y, Z, Z.sup.1, W, and (aa) are as defined as set forth in the specification. Provided are also compounds of Formula (I-A) for use to treat a condition or disorder responsive to Mcl-1 inhibition such as cancer. ##STR00001##
Inhibitors of KEAP1-Nrf2 protein-protein interaction
Sultam compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with the KEAP1-Nrf2 interaction, such as inflammatory bowel disease, including Crohn's disease and ulcerative colitis.
Inhibitors of KEAP1-Nrf2 protein-protein interaction
Sultam compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with the KEAP1-Nrf2 interaction, such as inflammatory bowel disease, including Crohn's disease and ulcerative colitis.
Processes and intermediates for preparing MCL1 inhibitors
The present disclosure provides methods for preparing MCL1 inhibitors or a salt thereof and related key intermediates.
Compounds that inhibit MCL-1 protein
- Sean P. Brown ,
- David Karl BEDKE ,
- Michael R. DeGraffenreid ,
- Jiasheng Fu ,
- Zhihong Li ,
- Felix Gonzalez Lopez De Turiso ,
- Ana Gonzalez Buenrostro ,
- Michael W. Gribble, Jr. ,
- Michael G. Johnson ,
- Todd J. KOHN ,
- Kexue LI ,
- Yunxiao LI ,
- Mike Elias Lizarzaburu ,
- Yosup Rew ,
- Joshua TAYGERLY ,
- Yingcai Wang ,
- Xuelei Yan ,
- Ming Yu ,
- Jiang Zhu ,
- Manuel Zancanella ,
- Xian Yun Jiao ,
- Liusheng Zhu ,
- Xianghong Wang ,
- Julio C. Medina ,
- Jason A. Duquette ,
- Jonathan B. HOUZE ,
- Marc VIMOLRATANA ,
- Mario G. Cardozo ,
- Alan C. Cheng
Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, ##STR00001##
and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.
Processes and intermediates for preparing MCL1 inhibitors
The present disclosure provides methods for preparing MCL1 inhibitors or a salt thereof and related key intermediates.
SPIROCYCLIC INHIBITORS OF HEPATITIS B VIRUS
The present invention relates to compounds that are inhibitors of hepatitis B virus (HBV). Compounds of this invention are useful alone or in combination with other agents for treating, ameliorating, preventing or curing HBV infection and related conditions. The present invention also relates to pharmaceutical compositions containing the compounds.
PROCESSES AND INTERMEDIATES FOR PREPARING MCL1 INHIBITORS
The present disclosure provides methods for preparing MCL1 inhibitors or a salt thereof and related key intermediates.