Dihydrochlamydocin analog-1 is a potent histone deacetylase (HDAC) inhibitor that demonstrates significant activity by inhibiting histone H4 peptide deacetylation with an IC50 of 30 nM. This compound is useful for studying the role of HDACs in gene regulation, cellular differentiation, and cancer therapy. It may also serve as a valuable tool in epigenetic research and therapeutic development targeting HDAC-related disorders.
Dihydrochlamydocin analog-1 is a potent histone deacetylase (HDAC) inhibitor that demonstrates significant activity by inhibiting histone H4 peptide deacetylation with an IC50 of 30 nM. This compound is useful for studying the role of HDACs in gene regulation, cellular differentiation, and cancer therapy. It may also serve as a valuable tool in epigenetic research and therapeutic development targeting HDAC-related disorders.
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