Cat.No.: | BSM-0398 |
Product Name: | CAY10398 |
CAS No.: | 193551-00-7 |
Figure: |
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Synonyms: | MD 85; PX 089274 |
Product Overview: | A potent, cost-effective histone deacetylase inhibitor |
Description: | CAY10398 is an inhibitor of histone deacetylase (HDAC1) with an IC50 value of 10 µM. Similar potency is observed with trapoxin A and B, whereas trichostatin A is more potent inhibitor of the enzyme. Trichostatin A also selectively inhibits the removal of acetyl groups from the amino-terminal lysine residues of core histones, which modulates the access of transcription factors to the underlying genomic DNA. However, trichostatin A is much more expensive than CAY10398. CAY10398 thus represents a selective and cost-effective compound for the inhibition of HDAC. |
Appearance: | A crystalline solid |
Molecular Weight: | 293.4 |
Purity: | ≥98% |
Storage: | -20°C |
Targets: | HDAC |
Molecular Formula: | C15H23N3O3 |
Chemical Name: | 4-(dimethylamino)-N-[6-(hydroxyamino)-6-oxohexyl]-benzamide |
Warning: | For Research Use Only! Not For Use in Humans. |
Product Types | ||
◆ Extracts & Lysates | ||
EL-0006 | Recombinant Human HDAC1 293 Cell Lysate | Inquiry |
EL-0007 | Recombinant Human HDAC2 293 Cell Lysate | Inquiry |
EL-0008 | Recombinant Human HDAC3 Cell Lysate | Inquiry |
EL-0009 | Recombinant Human HDAC4 Cell Lysate | Inquiry |
◆ Bioactive Small Molecules | ||
BSM-0007 | Tubacin | Inquiry |
Related Gene / Proteins | |||
HDAC | HDAC1 | HDAC10 | HDAC11 |
HDAC2 | HDAC3 | hdac4 | hdac5 |
HDAC6 | hdac7 | HDAC8 | hdac9 |
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