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FT895

Catalog No. T11329   CAS 2225728-57-2

FT895 is a selective and potent HDAC11 inhibitor with antifungal and antitumor activity that inhibits HDAC11 expression and limits EV71 replication in vitro.

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FT895 Chemical Structure
FT895, CAS 2225728-57-2
Pack Size Availability Price/USD Quantity
25 mg 8-10 weeks $ 766.00
50 mg 8-10 weeks $ 995.00
100 mg 8-10 weeks $ 1,560.00
1 mL * 10 mM (in DMSO) 8-10 weeks $ 322.00
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This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
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Purity: 99.81%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description FT895 is a selective and potent HDAC11 inhibitor with antifungal and antitumor activity that inhibits HDAC11 expression and limits EV71 replication in vitro.
Targets&IC50 HDAC11:3 nM
In vitro FT895 is a highly selective inhibitor of HDAC11, exhibiting over 1000-fold selectivity against the other 10 members of the HDAC family[1].
Molecular Weight 352.31
Formula C16H15F3N4O2
CAS No. 2225728-57-2

Storage

store at low temperature

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 20 mg/mL (56.77 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Martin MW, et al. Discovery of novel N-hydroxy-2-arylisoindoline-4-carboxamides as potent and selective inhibitors of HDAC1Bioorg Med Chem Lett. 2018 Jul 1;28(12):2143-2147.

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Keywords

FT895 2225728-57-2 Chromatin/Epigenetic DNA Damage/DNA Repair Microbiology/Virology HDAC Antifungal FT 895 FT-895 inhibitor inhibit

 

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