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Oxatomide

Catalog No. T19839   CAS 60607-34-3
Synonyms: Oxatomida

Oxatomide (Oxatomida) is a potent and orally active dual H1 histamine receptor and P2X7 receptor antagonist with antihistamine and antiallergic activity.Oxatomide can be used to block ATP-induced currents in the human P2X7 receptor with an IC50 value of 0.95 μM.Oxatomide has an inhibitory effect on ATP-induced Ca2+ inward currents with an IC50 value of 0.43 μM.Oxatomide inhibits 5-hydroxytryptamine. Oxatomide inhibits 5-hydroxytryptamine with an IC50 of 0.43 μM.Oxatomide is used in the treatment of immune system diseases and in the study of hypersensitivity reactions.

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Oxatomide Chemical Structure
Oxatomide, CAS 60607-34-3
Pack Size Availability Price/USD Quantity
1 mg In stock $ 41.00
5 mg In stock $ 97.00
10 mg In stock $ 163.00
25 mg In stock $ 313.00
50 mg In stock $ 497.00
100 mg In stock $ 788.00
500 mg In stock $ 1,590.00
1 mL * 10 mM (in DMSO) In stock $ 107.00
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Purity: 98.93%
Purity: 98.61%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Oxatomide (Oxatomida) is a potent and orally active dual H1 histamine receptor and P2X7 receptor antagonist with antihistamine and antiallergic activity.Oxatomide can be used to block ATP-induced currents in the human P2X7 receptor with an IC50 value of 0.95 μM.Oxatomide has an inhibitory effect on ATP-induced Ca2+ inward currents with an IC50 value of 0.43 μM.Oxatomide inhibits 5-hydroxytryptamine. Oxatomide inhibits 5-hydroxytryptamine with an IC50 of 0.43 μM.Oxatomide is used in the treatment of immune system diseases and in the study of hypersensitivity reactions.
In vitro Oxatomide almost completely blocks the ATP-induced current in human P2X7 receptors (IC50 of 0.95 μM). Oxatomide inhibits ATP-induced Ca2+ influx with an IC50 value of 0.43 μM and also inhibits serotonin.[1]
Synonyms Oxatomida
Molecular Weight 426.55
Formula C27H30N4O
CAS No. 60607-34-3

Storage

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

Solubility Information

DMSO: 170.62 mg/mL (400 mM)

TargetMolReferences and Literature

1. Yoshida K, et al. P2X7 receptor antagonist activity of the anti-allergic agent oxatomide. Eur J Pharmacol. 2015;767:41-51. 2. Ohmori K, et al. Pharmacological studies on oxatomide (KW-4354). (7) Antagonistic effects on chemical mediators. Nihon Yakurigaku Zasshi. 1983;81(5):399-409. 3. Raschi E, et al. The Contribution of National Spontaneous Reporting Systems to Detect Signals of Torsadogenicity: Issues Emerging from the ARITMO Project. Drug Saf. 2016 Jan;39(1):59-68. 4. Curtin Whelan L, Geary M, Sweetman P. Development and validation of a rapid liquid chromatographic method for the determination of oxatomide and its related impurities. J Chromatogr Sci. 2014 Nov-Dec;52(10):1267-72.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Approved Drug Library Anti-Cancer Drug Library Anti-Cancer Clinical Compound Library GPCR Compound Library Membrane Protein-targeted Compound Library Drug Repurposing Compound Library FDA-Approved & Pharmacopeia Drug Library Approved Drug Library Bioactive Compound Library Neurotransmitter Receptor Compound Library

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Keywords

Oxatomide 60607-34-3 GPCR/G Protein Immunology/Inflammation Membrane transporter/Ion channel Metabolism Neuroscience Calcium Channel P2X Receptor 5-HT Receptor Histamine Receptor Oxatomida inhibitor inhibit

 

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