Chemical Structure : MC1742
CAS No.: 1776116-74-5
Catalog No.: PC-27699Not For Human Use, Lab Use Only.
MC1742 is a potent HDAC inhibitor with IC50s of 0.1 μM, 0.11 μM, 0.02 μM, 0.007 μM, 0.61 μM, 0.04 μM and 0.1 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, HDAC10 and HDAC11, respectively, also potently reactivate HIV from latency.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
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| 10 mg | $128 | In stock | |
| 25 mg | $198 | In stock | |
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MC1742 is a potent HDAC inhibitor with IC50s of 0.1 μM, 0.11 μM, 0.02 μM, 0.007 μM, 0.61 μM, 0.04 μM and 0.1 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, HDAC10 and HDAC11, respectively, also potently reactivate HIV from latency with EC50 of 350 nM.
MC1742 increases acetyl-H3 and acetyl-tubulin levels and inhibits cancer stem cells growth.
MC1742 induces growth arrest, apoptosis, and differentiation in sarcoma cancer stem cells (CSCs).
MC1742 also blocks Toxoplasma gondii tachyzoite growth and profoundly disrupts parasite gene expression.
| M.Wt | 395.48 | |
| Formula | C21H21N3O3S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
5-((4-([1,1'-Biphenyl]-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl)thio)-N-hydroxypentanamide |
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1. Di Pompo G, et al. J Med Chem. 2015 May 14;58(9):4073-9.
2. Mouveaux T, et al. Int J Antimicrob Agents. 2022 Mar;59(3):106526.

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