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Merck
CN

1379401

USP

美洛昔康

United States Pharmacopeia (USP) Reference Standard

别名:

4-羟基-2-甲基- N -(5-甲基-2-噻唑基)-2 H -1,2-苯并噻嗪-3-甲酰胺 1,1-二氧化物

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关于此项目

经验公式(希尔记法):
C14H13N3O4S2
化学文摘社编号:
分子量:
351.40
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24
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InChI

1S/C14H13N3O4S2/c1-8-7-15-14(22-8)16-13(19)11-12(18)9-5-3-4-6-10(9)23(20,21)17(11)2/h3-7,19H,1-2H3,(H,15,16)/b13-11+

InChI key

DWMREKMVXIFPFM-ACCUITESSA-N

grade

pharmaceutical primary standard

API family

meloxicam

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

format

neat

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General description

本产品按照发行药典的发行和规定提供。支持本产品的所有信息,包括安全数据表和任何产品信息传单,都是在发行药典的授权下开发和发布的。如需进一步信息和支持,请访问现行药典网站。

Application

美洛昔康USP参标准品,预期用途是USP规定的指定质量测试和检测。也用于USP各论,例如:
  • 美洛昔康口服混悬液
  • 美洛昔康片

Analysis Note

这些产品仅供测试和化验使用。它们不适用于人类或动物,也不能用于诊断、治疗或治愈任何类型的疾病。

Other Notes

可能适用相应的销售限制。

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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[Meloxicam (Movalis)].
Dusanka Martinović Kaliterna
Reumatizam, 54(2), 81-82 (2008-03-21)
D Türck et al.
British journal of rheumatology, 35 Suppl 1, 13-16 (1996-04-01)
Meloxicam is a new preferential cyclooxygenase-2 (COX-2) inhibitor currently for the treatment of osteoarthritis and rheumatoid arthritis. Its pharmacokinetic profile is characterized by a prolonged and almost complete absorption and the drug is > 99.5% bound to plasma proteins. Meloxicam
G Engelhardt
British journal of rheumatology, 35 Suppl 1, 4-12 (1996-04-01)
This review focuses on the key pharmacological findings with a new NSAID, meloxicam. Unlike established NSAIDs, it preferentially inhibits inducible COX-2 in guinea-pigs peritoneal macrophages and human COX-2 in COS cells. Compared with other NSAIDs, meloxicam is the most potent
D E Furst
Seminars in arthritis and rheumatism, 26(6 Suppl 1), 21-27 (1997-06-01)
Nonsteroidal antiinflammatory drugs (NSAIDs) exert their actions by inhibiting cyclooxygenase (COX). It has recently been postulated that NSAIDs' antiinflammatory efficacy arises from inhibition of the COX-2 isoform of cyclooxygenase, whereas inhibition of the COX-1 isoform produces the troublesome and sometimes
[Efficacy and intolerance of meloxicam in injection and tablet form].
V P Tiurin et al.
Voenno-meditsinskii zhurnal, 324(11), 54-58 (2004-01-17)

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