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Merck
CN

D8890

安乃近

analytical standard

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关于此项目

线性分子式:
C13H16N3O4SNa
化学文摘社编号:
分子量:
333.34
UNSPSC Code:
41116107
PubChem Substance ID:
EC Number:
200-694-7
MDL number:
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grade

analytical standard

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

forensics and toxicology
veterinary

format

neat

storage temp.

2-8°C

SMILES string

[Na].CN(CS(O)(=O)=O)C1=C(C)N(C)N(C1=O)c2ccccc2

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem/physiol Actions

非甾体抗炎药,与吗啡并服时,能增强镇痛作用,延缓耐受。安乃近是环氧酶-3 (COX-3) 具有相对选择性的抑制剂,对 COX-1 的活性较低,对 COX-2 没有活性。以几种模式阻止 PGE2 引起的痛觉过敏。


pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Joel E Schlosburg et al.
Behavioural pharmacology, 23(7), 722-726 (2012-09-08)
Dipyrone is a common nonopioid analgesic and antipyretic, which, in many countries, is available over the counter and is more widely used than paracetamol or aspirin. However, the exact mechanisms by which dipyrone acts remain inconclusive. Two novel arachidonoyl-conjugated metabolites
Márcia Germana Alves de Araújo Lobo et al.
BMC pharmacology & toxicology, 14, 5-5 (2013-01-10)
Adverse drug reactions (ADRs) are recognised as a common cause of hospital admissions, and they constitute a significant economic burden for hospitals. Hospital-based ADR monitoring and reporting programmes aim to identify and quantify the risks associated with the use of
M Levy et al.
Clinical pharmacokinetics, 28(3), 216-234 (1995-03-01)
The pharmacokinetics of dipyrone are characterised by rapid hydrolysis to the active moiety 4-methyl-amino-antipyrine (MAA), which has 85% bioavailability after oral administration in tablet form, and takes a short time to achieve maximal systemic concentrations (tmax of 1.2 to 2.0