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MC1742

Chemical Structure : MC1742

CAS No.: 1776116-74-5

MC1742 (MC-1742)

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.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 395.48
Formula C21H21N3O3S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
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

References

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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