DCC-3116 25mg | Purity Not Available
Selleck Chemicals
DCC-3116 is a selective inhibitor of ULK1/2 that blocks both basal and sotorasib-induced autophagy in KRAS G12C-driven cell lines and exhibits anti-tumor activity.
More Information Supplier PageDCC-3116 is a selective inhibitor of ULK1/2 that blocks both basal and sotorasib-induced autophagy in KRAS G12C-driven cell lines and exhibits anti-tumor activity.
More Information Supplier PageDCC-3116 is a selective inhibitor of ULK1/2 that blocks both basal and sotorasib-induced autophagy in KRAS G12C-driven cell lines and exhibits anti-tumor activity.
More Information Supplier PagePevonedistat hydrochloride (MLN4924 hydrochloride) is a potent and selective inhibitor of NEDD8-activating enzyme (NAE) with an IC50 of 4.7 nM. It disrupts cullin-RING ligase-mediated protein degradation, leading to apoptotic cell death in human tumor cells through the deregulation of S-phase DNA synthesis.
More Information Supplier PageBLU-222 is an oral, potent, and selective inhibitor of cyclin-dependent kinase (CDK) 2 and exhibits significant antitumor activity in the OVCAR-3 CDX model.
More Information Supplier PageBLU-222 is an oral, potent, and selective inhibitor of cyclin-dependent kinase (CDK) 2 and exhibits significant antitumor activity in the OVCAR-3 CDX model.
More Information Supplier PageBLU-222 is an oral, potent, and selective inhibitor of cyclin-dependent kinase (CDK) 2 and exhibits significant antitumor activity in the OVCAR-3 CDX model.
More Information Supplier PageBLU-222 is an oral, potent, and selective inhibitor of cyclin-dependent kinase (CDK) 2 and exhibits significant antitumor activity in the OVCAR-3 CDX model.
More Information Supplier PageX5050 is a benzoimidazole-5-carboxamide derivative and a potent inhibitor of repressor element-1 silencing transcription factor (REST) with an EC50 of 2.1 μM. It can be used in research of Huntington’s disease and other neurodegenerative disorders characterized by altered BDNF levels.
More Information Supplier PageX5050 is a benzoimidazole-5-carboxamide derivative and a potent inhibitor of repressor element-1 silencing transcription factor (REST) with an EC50 of 2.1 μM. It can be used in research of Huntington’s disease and other neurodegenerative disorders characterized by altered BDNF levels.
More Information Supplier PageX5050 is a benzoimidazole-5-carboxamide derivative and a potent inhibitor of repressor element-1 silencing transcription factor (REST) with an EC50 of 2.1 μM. It can be used in research of Huntington’s disease and other neurodegenerative disorders characterized by altered BDNF levels.
More Information Supplier Page