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FMK 9a

Catalog No. T15303   CAS 1955550-51-2

FMK 9a is an irreversible inhibitor of ATG4B with IC50 values of 80 and 73 nM in the TR-FRET and cellular-based LRA assays.

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FMK 9a Chemical Structure
FMK 9a, CAS 1955550-51-2
Pack Size Availability Price/USD Quantity
1 mg In stock $ 142.00
5 mg In stock $ 347.00
10 mg In stock $ 519.00
25 mg In stock $ 842.00
50 mg In stock $ 1,160.00
100 mg In stock $ 1,570.00
500 mg In stock $ 3,130.00
1 mL * 10 mM (in DMSO) In stock $ 298.00
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Purity: 98.97%
ee: 100%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description FMK 9a is an irreversible inhibitor of ATG4B with IC50 values of 80 and 73 nM in the TR-FRET and cellular-based LRA assays.
Targets&IC50 Autophagin-1 (FRET assay):80 nM, Autophagin-1 (LRA assay):73 nM
In vitro FMK 9a forms a covalent bond with the more reactive thiol group of Cys74 located at the catalytic site of ATG4B thereby inactivating ATG4B proteolytic activity[1].
In vivo FMK 9a shows moderate solubility and high liver microsome clearances for human and mice of 13.9 and 70 mL/kg/min[1].
Molecular Weight 392.42
Formula C23H21FN2O3
CAS No. 1955550-51-2

Storage

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

Solubility Information

DMSO: 95 mg/mL (242.09 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Qiu Z, et al. Discovery of Fluoromethylketone-Based Peptidomimetics as Covalent ATG4B (Autophagin-1) Inhibitors. ACS Med Chem Lett. 2016 Jun 25;7(8):802-6.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Bioactive Compounds Library Max Autophagy Compound Library Bioactive Compound Library

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Keywords

FMK 9a 1955550-51-2 Autophagy Proteases/Proteasome Cysteine Protease inhibit Inhibitor inhibitor

 

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