research use only

AK 7 Sirtuin inhibitor

Cat.No.S5914

AK 7 is a brain-permeable selective SIRT2 inhibitor with an IC50 of 15.5 μM.
AK 7 Sirtuin inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 437.35

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 437.35 Formula

C19H21BrN2O3S

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 420831-40-9 -- Storage of Stock Solutions

Synonyms N/A Smiles C1CCCN(CC1)S(=O)(=O)C2=CC=CC(=C2)C(=O)NC3=CC(=CC=C3)Br

Solubility

In vitro
Batch:

DMSO : 87 mg/mL (198.92 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 3 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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%DMSO %

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
SIRT2 [1]
15.5 μM
In vitro

Treatment with AK7 increases lysine 40 (K40) acetylation of α-tubulin in neuronal cells. AK7 ameliorates alpha-synuclein toxicity in vitro[1].

In vivo

AK7 is neuroprotective in models of Parkinson's disease and prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced dopamine depletion and dopaminergic neuron loss in vivo. AK7 does not show beneficial effects in mouse models of amyotrophic lateral sclerosis and cerebral ischemia[1].

References

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