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Tofisopam

Catalog No. T34896   CAS 22345-47-7
Synonyms: Emandaxin, Grandaxin

Tofisopam (Grandaxin) is a 2,3-benzodiazepine compound with anxiolytic activity that can be taken orally.

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Tofisopam Chemical Structure
Tofisopam, CAS 22345-47-7
Pack Size Availability Price/USD Quantity
1 mg In stock $ 33.00
5 mg In stock $ 68.00
10 mg In stock $ 98.00
25 mg In stock $ 177.00
50 mg In stock $ 253.00
100 mg In stock $ 372.00
200 mg In stock $ 545.00
1 mL * 10 mM (in DMSO) In stock $ 85.00
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Purity: 99.59%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Tofisopam (Grandaxin) is a 2,3-benzodiazepine compound with anxiolytic activity that can be taken orally.
In vivo Tofisopam (30 and 100 mg/kg, po) significantly inhibited the gastric ulceration induced by water-immersion stress in normal rats in a dose-dependent manner. Immobilization-stress loading increased the incidence and average index of gastric ulceration in OB rats, compared with nonstressed rats. Tofisopam (100 mg/kg, po) significantly inhibited the gastric ulceration induced by stress loading in OB rats. Water-immersion stress loading induced a significant increase in intestinal propulsion in rats. This increase was reversed to control levels by tofisopam (100 mg/kg, po). Tofisopam (1.0 mg/kg, iv, or 0.1 mg/kg by intracerebrospinal injection) inhibited the constriction of ear microvessels, the decrease in earlobe temperature, and mydriasis induced by electrical stimulation of the medial hypothalamic area in rabbits[2].
Synonyms Emandaxin, Grandaxin
Molecular Weight 382.45
Formula C22H26N2O4
CAS No. 22345-47-7

Storage

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

Solubility Information

DMSO: 50 mg/mL (130.74 mM)

TargetMolReferences and Literature

1. Hatayama M, Sumida C, Kurajoh M, Shiraishi J, Okazaki H, Shoji T, Koyama H, Tsutsumi Z, Moriwaki Y, Namba M, Yamamoto T. Acute Effects of Oral Tofisopam on Plasma Concentration and Urinary Excretion of Uric Acid and Oxypurinol. Curr Clin Pharmacol. 2015 Jan 26. [Epub ahead of print] PubMed PMID: 25619490. 2. Ramadan NK, Mohamed AO, Fouad RM, Moustafa AA. Different techniques for the determination of tofisopam. J AOAC Int. 2014 Jan-Feb;97(1):105-13. PubMed PMID: 24672866. 3. Abrushanian ÉB, Popov AV. [Pineal hormone melatonin in low doses potentiates psychotropic and chronotropic activity of tofisopam in rats]. Eksp Klin Farmakol. 2013;76(4):15-7. Russian. PubMed PMID: 23762983. 4. Bihel FJ, Justiniano H, Schmitt M, Hellal M, Ibrahim MA, Lugnier C, Bourguignon JJ. New PDE4 inhibitors based on pharmacophoric similarity between papaverine and tofisopam. Bioorg Med Chem Lett. 2011 Nov 1;21(21):6567-72. doi: 10.1016/j.bmcl.2011.08.036. Epub 2011 Aug 12. PubMed PMID: 21920746.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Bioactive Compound Library Human Metabolite Library FDA-Approved & Pharmacopeia Drug Library Bioactive Compounds Library Max Approved Drug Library Orally Active Compound Library

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Keywords

Tofisopam 22345-47-7 Others Emandaxin anxiolytic agent inhibit orally active Inhibitor Grandaxin inhibitor

 

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