
CAS 936221-33-9
:CG200745
Description:
CG200745, with the CAS number 936221-33-9, is a chemical compound that has garnered attention in pharmaceutical research, particularly in the context of cancer treatment. It is classified as a small molecule inhibitor, specifically targeting certain kinases involved in cellular signaling pathways that regulate cell growth and proliferation. The compound exhibits selective inhibition, which is crucial for minimizing off-target effects and enhancing therapeutic efficacy. CG200745 is typically characterized by its molecular structure, which includes specific functional groups that contribute to its biological activity. In terms of solubility, it is often evaluated in various solvents to determine its bioavailability and pharmacokinetic properties. Additionally, studies on CG200745 may include its stability under different conditions, potential side effects, and mechanisms of action within cellular systems. Overall, CG200745 represents a promising candidate in the development of targeted therapies for specific types of cancer, reflecting the ongoing efforts in medicinal chemistry to design effective and selective therapeutic agents.
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Found 3 products.
CG 200745
CAS:<p>CG 200745 is a histone protein-conjugate that inhibits the activity of mammalian target of rapamycin complex 1 (mTORC1) and specifically increases acetylation of the histones H3 and H4. This drug has been shown to have cardioprotective effects in a number of preclinical models, including cardiac hypertrophy and heart failure. CG 200745 also has anti-cancer effects when used in combination with other medicines. It has shown efficacy against cancer cells through inhibition of histone deacetylases (HDACs).</p>Formula:C24H33N3O4Purity:Min. 95%Molecular weight:427.5 g/molIvaltinostat
CAS:CG-200745 is a potent inhibitor of HDAC. CG200745 induces apoptosis and also inhibits the deacetylation of histone H3 and tubulin.Formula:C24H33N3O4Purity:98%Color and Shape:SolidMolecular weight:427.54


