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Lornoxicam-D4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam (T1468) is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID)with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells,which endogenously express COX-1,as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells,which endogenously express COX-2. Lornoxicam (T1468)reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50 values 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. Formulations containing lornoxicam have been used in the management of postoperative pain.
Lornoxicam-D4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam (T1468) is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID)with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells,which endogenously express COX-1,as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells,which endogenously express COX-2. Lornoxicam (T1468)reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50 values 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. Formulations containing lornoxicam have been used in the management of postoperative pain.

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 1,230 | 35日内发货 | |
| 5 mg | ¥ 4,530 | 35日内发货 | |
| 10 mg | ¥ 8,430 | 35日内发货 |
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| 产品描述 | Lornoxicam-D4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam (T1468) is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously express COX-2. Lornoxicam (T1468) reduces LPS-induced production of nitric oxide and IL-6 in cell-based assays with IC50 values 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. Formulations containing lornoxicam have been used in the management of postoperative pain. |
| 分子量 | 375.85 |
| 分子式 | C13H6ClD4N3O4S2 |
| CAS No. | 1216527-48-8 |
| Smiles | OC=1C2=C(S(=O)(=O)N(C)C1C(NC3=C(C(=C(C(=N3)[2H])[2H])[2H])[2H])=O)C=C(Cl)S2 |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. 实际储存温度请以COA为准 |
对于不同动物的给药剂量换算,您也可以参考 更多