sudoxicam
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- CAS号:
- 34042-85-8
- 英文名:
- sudoxicam
- 英文别名:
- CP-15973;4-Hydroxy-2-methyl-3-(2-thiazolylcarbamoyl)-2H-1,2-benzothiazine 1,1-dioxide;4-Hydroxy-2-methyl-N-(thiazol-2-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide;2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-2-thiazolyl-, 1,1-dioxide;4-hydroxy-2-methyl-1,1-dioxo-N-(1,3-thiazol-2-yl)-1$l^{6},2-benzothiazine-3-carboxamide
- 中文名:
- sudoxicam
- 中文别名:
- 化合物 T16950
- CBNumber:
- CB5937877
- 分子式:
- C13H11N3O4S2
- 分子量:
- 337.379
- MOL File:
- 34042-85-8.mol
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sudoxicam化学性质
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熔点:
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240-243°C (dec.)
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储存条件:
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Refrigerator
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溶解度:
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DMSO : 83.33 mg/mL (247.00 mM; ultrasonic and warming and heat to 80°C)
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形态:
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Solid
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颜色:
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Brown
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sudoxicam性质、用途与生产工艺
Sudoxicam 是一种可逆的口服活性的 COX 拮抗剂,是烯醇-羧酰胺类的非甾体抗炎药 (NSAID)。Sudoxicam 具有有效的抗炎,抗浮肿和退热作用。
Sudoxicam demonstrates NADPH-dependent covalent binding to human liver microsomes. With addition of glutathione (GSH) in microsomal incubations, about half of the covalent incorporation of Sudoxicam is blocked by addition of GSH.
Metabolite identification studies on [14C]-Sudoxicam in NADPH-supplemented human liver microsomes indicated that the primary route of metabolism involved a P450-mediated thiazole ring scission to the corresponding acylthiourea metabolite (S3), a well-established pro-toxin.
In vitro, Sudoxicam underwent the oxidative thiazole-open biotransformation, resulting in the formation of an acylthiourea and the subsequent hydroxylated metabolite.
Sudoxicam (1-10 mg/kg; oral administration; daily; for 7 days; rats) treatment effective reduces plasma inflammation units, reduces the swelling of inflamed hind-paws and restores toward normal the daily gain in body weight.
In the intact rat, Sudoxicam significantly inhibited edema formation at doses as low as 0.1 mg/kg, p.o.
Sudoxicam inhibits the erythema caused by ultraviolet irradiation in the guinea pig.
Sudoxicam (3.3 mg/kg, i.p.) is capable of counteracting the pyrexia induced by the intraperitoneal injection of typhoid/paratyphoid vaccine in rats, maintaining body temperature about that of uninjected control rats.
The plasma half-life of Sudoxicam ranged between 8 hours (monkey), 13 hours (rat), and 60 hours (dog).
Animal Model:
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Rats injected with ,i>M. butyrieum
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Dosage:
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1 mg/kg, 3.3 mg/kg, 10 mg/kg
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Administration:
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Oral administration; daily; for 7 days
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Result:
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Were both effective in reducing plasma inflammation units, in reducing the swelling of inflamed hind-paws.
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sudoxicam
上下游产品信息
上游原料
下游产品
34042-85-8, sudoxicam 相关搜索:
- Sulfur & Selenium Compounds
- Pharmaceuticals
- Intermediates & Fine Chemicals
- Heterocycles
- 化合物 T16950
- 34042-85-8
- 2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-2-thiazolyl-, 1,1-dioxide
- 4-hydroxy-2-methyl-1,1-dioxo-N-(1,3-thiazol-2-yl)-1$l^{6},2-benzothiazine-3-carboxamide
- CP-15973
- 4-Hydroxy-2-methyl-N-(thiazol-2-yl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
- 4-Hydroxy-2-methyl-3-(2-thiazolylcarbamoyl)-2H-1,2-benzothiazine 1,1-dioxide