Tepoxalin [103475-41-8]

Referência 021361-10mg

Tamanho : 10mg

Marca : US Biological



021361 Tepoxalin

Grade
Highly Purified
Shipping Temp
RT
Storage Temp
4°C

Non-steroidal anti-inflammatory drug (NSAID) with potent anti-inflammatory and analgesic properties approved for veterinary use. It has inhibitory effect on cyclooxygenase and 5-lipxygenase activity as well as inhibiting the production of cytokines in peripheral cells outside the CNS. Tepoxalin, also known as ORF-20485; RWJ-20485; is a 5-lipoxygenase inhibitor potentially for the treatment of asthma, osteoarthritis (OA). Tepoxalin has in vivo inhibitory activity against COX-1, COX-2, and 5-LOX in dogs at the current approved recommended dosage.Tepoxalin inhibits inflammation and microvascular dysfunction induced by abdominal irradiation in rats. Tepoxalin enhances the activity of an antioxidant, pyrrolidine dithiocarbamate, in attenuating tumor necrosis factor alpha-induced apoptosis in WEHI 164 cells.

Synonyms:
5-(4-Chlorophenyl)-N-hydroxy-1-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-propanamide; ORF 20485; RWJ 20485

CAS No:
103475-41-8

Molecular Formula:
C₂₀H₂₀ClN₃O₃

Molecular Weight:
385.84

Appearance:
White to off-white solid

Purity:
As reported

Melting Point:
123-125°C

Solubility:
DMSO, Methanol

Storage:
4°C, Hygroscopic, Under Inert Atmosphere

Applications
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures.
Form
White to off-white solid
Purity
As reported
References
Argentieri, D.C. et al.: J. Pharmacol. Exp. Therap., 271, 1399 (1994); Agnello, K.A. et al.: Am. J. Vet. Res., 66, 966 (2005); Fiebich, B.L. et al.: Neuropharmacol., 38, 1325 (1999)

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