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Niflumic Acid

产品号 DB04552 公司名称 DrugBank
CAS号 4394-00-7 公司网站 http://www.ualberta.ca/
分子式 C13H9F3N2O2 电 话 (780) 492-3111
分子量 282.2179696 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 4120

产品价格信息

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产品别名

标题
Niflumic Acid
IUPAC标准名
2-{[3-(trifluoromethyl)phenyl]amino}pyridine-3-carboxylic acid
IUPAC传统名
niflumic acid
商标名
Forenol
Actol
Flogovital
Niflam
Nifluril
Landruma
别名
2-[3-(Trifluoromethyl)anilino]nicotinic acid
Nifluminic acid
Acido niflumico [inn-spanish]
Acidum niflumicum [inn-latin]
2-[(3-Trifluoromethyl)Phenyl]Amino-3-Pyridine-Carboxylic Acid
NFL
2-(alpha,alpha,alpha-Trifluoro-m-toluidino)nicotinic acid
2-(3-Trifluoromethyl-phenylamino)-nicotinic acid
2-(3-(Trifluoromethyl)-phenyl)aminonicotinic acid
Niflumate
NFA
Lopac-N-0630
Acide niflumique [inn-french]
2-(3-(Trifluoromethyl)anilino)nicotinic acid

产品登记号

PubChem SID 46504657
CAS号 4394-00-7
PubChem CID 4488

产品性质

疏水性(logP) 4.43 [TAKACS-NOVAK,K ET AL. (1995)]
溶解度 0.019 mg/mL at 25 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description An analgesic and anti-inflammatory agent used in the treatment of rheumatoid arthritis. [PubChem]
Indication Used in the treatment of rheumatoid arthritis.
Pharmacology Niflumic acid, a nonsteroidal anti-inflammatory fenamate, is a Ca2+-activated Cl- channel blocker.
Toxicity Oral, mouse: LD50 = 350 mg/kg; Oral, rat: LD50 = 250 mg/kg
Affected Organisms
Humans and other mammals
Biotransformation Hepatic.
Absorption Well absorbed following oral administration.
Half Life 2.5 hours
Protein Binding 90% bound to plasma proteins.
References
Criddle DN, de Moura RS, Greenwood IA, Large WA: Inhibitory action of niflumic acid on noradrenaline- and 5-hydroxytryptamine-induced pressor responses in the isolated mesenteric vascular bed of the rat. Br J Pharmacol. 1997 Mar;120(5):813-8. [Pubmed]

参考文献

  • Criddle DN, de Moura RS, Greenwood IA, Large WA: Inhibitory action of niflumic acid on noradrenaline- and 5-hydroxytryptamine-induced pressor responses in the isolated mesenteric vascular bed of the rat. Br J Pharmacol. 1997 Mar;120(5):813-8. Pubmed