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Lornoxicam-d4
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Lornoxicam-d4图片
规格:98%
分子量:375.8
包装与价格:
包装价格(元)
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An internal standard for the quantification of lornoxicam
货号:ajcx24394
CAS:1216527-48-8
分子式:C13H6ClD4N3O4S2
分子量:375.8
溶解度:DMSO: 2 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Lornoxicam-d4is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties.1It inhibits production of thromboxane B2from arachidonic acid in HEL human erythroleukemic cells (IC50= 3 nM), which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin Ffrom arachidonic acid in Mono-Mac-6 cells (IC50= 8 nM), which endogenously express COX-2. Lornoxicam reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50values of 65 and 54 µM, respectively. It reduces carrageenan-induced paw edema in rats when administered intravenously at doses ranging from 0.1 to 9 mg/kg.2Formulations containing lornoxicam have been used in the management of postoperative pain.


1.Berg, J., Fellier, H., Christoph, T., et al.The analgesic NSAID lornoxicam inhibits cyclooxygenase (COX)-1/-2, inducible nitric oxide synthase (iNOS), and the formation of interleukin (IL)-6 in vitroInflamm. Res.48(7)369-379(1999) 2.Buritova, J., and Besson, J.M.Potent anti-inflammatory/analgesic effects of lornoxicam in comparison to other nsaids: A c-Fos study in the ratInflammopharmacology5(4)331-341(1997)

 
 
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