For research use only. We do not sell to patients.

MC4355

Biological Activity：MC4355 is a dual inhibitor of EZH2 and histone deacetylase (HDAC).

Research Area：Cancer

Targets：HDAC|Histone Methyltransferase

Related Screening Libraries:Bioactive Compound Library Plus;Cell Cycle/DNA Damage Compound Library;Epigenetics Compound Library;Histone Modification Research Compound Library;Anti-Cancer Compound Library;Anti-Aging Compound Library;Reprogramming Compound Library;Oxygen Sensing Compound Library;Anti-Breast Cancer Compound Library;Anti-Pancreatic Cancer Compound Library;Anti-Blood Cancer Compound Library;Anti-Liver Cancer Compound Library ;Osteogenesis Compound Library;Cancer Stem Cells Compound Library;

Related Small Molecules:EEDi-5285;EZH2-IN-2;BIX-01294;Pivanex;Crotonoside;MPT0B390;SGC707;(S)-HH2853;G9a-IN-1;RSC133;UNC4976;MS1943;HDAC1/6-IN-1;HDAC/HSP90-IN-4;JPS014;OTS186935 hydrochloride;HDAC-IN-4;MS8815;(R)-HH2853;HDAC-IN-27;EPZ020411;1-Alaninechlamydocin;Furamidine dihydrochloride;SKLB-23bb;Tacedinaline;EZH2-IN-12;UNC0642;MU1656

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Structurally and synthetically diverse biologically active compounds；

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