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Pinokalant

Catalog No. T70540   CAS 149759-26-2
Synonyms: LOE-908

Pinokalant (LOE-908) is a novel non-selective cation channel inhibitor.Pinokalant significantly reduces cortical infarct volume in in vivo experiments, improves the metabolic and electrophysiological status of the ischemic penumbra region, and reduces the size of the lesion on magnetic resonance images in the acute phase after middle cerebral artery occlusion in rats.Pinokalant is a potential SARS-CoV-2 protease inhibitor for the study of stroke.

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Pinokalant Chemical Structure
Pinokalant, CAS 149759-26-2
Pack Size Availability Price/USD Quantity
1 mg In stock $ 195.00
5 mg In stock $ 430.00
10 mg In stock $ 636.00
25 mg In stock $ 987.00
50 mg In stock $ 1,360.00
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Purity: 99.09%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Pinokalant (LOE-908) is a novel non-selective cation channel inhibitor.Pinokalant significantly reduces cortical infarct volume in in vivo experiments, improves the metabolic and electrophysiological status of the ischemic penumbra region, and reduces the size of the lesion on magnetic resonance images in the acute phase after middle cerebral artery occlusion in rats.Pinokalant is a potential SARS-CoV-2 protease inhibitor for the study of stroke.
In vitro Pinokalant leads to a substantial decrease in cortical infarct volume, reducing it from 33.8 mm³ to 24.5 mm³.[1]
Synonyms LOE-908
Molecular Weight 712.83
Formula C41H48N2O9
CAS No. 149759-26-2

Storage

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

TargetMolReferences and Literature

1. Christensen T, et al. The broad-spectrum cation channel blocker pinokalant (LOE 908 MS) reduces brain infarct volume in rats: a temperature-controlled histological study. Basic Clin Pharmacol Toxicol. 2005;96(4):316-324. 2. Simard JM, et al. Non-selective cation channels, transient receptor potential channels and ischemic stroke. Biochim Biophys Acta. 2007;1772(8):947-957. 3. Serdar Durdagi, et al. Screening of Clinically Approved and Investigation Drugs as Potential Inhibitors of SARS-CoV-2 Main Protease and Spike Receptor-Binding Domain Bound with ACE2 COVID19 Target Proteins: A Virtual Drug Repurposing Study. 2020.

Related compound libraries

This product is contained In the following compound libraries:
Membrane Protein-targeted Compound Library Inhibitor Library Bioactive Compound Library Bioactive Compounds Library Max

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Keywords

Pinokalant 149759-26-2 Membrane transporter/Ion channel Microbiology/Virology SARS-CoV TRP/TRPV Channel LOE-908 LOE 908 LOE908 inhibitor inhibit

 

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