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氟芬那酸530-78-9惠誠生物優勢供應

 
品牌: 進口
產品型號: 氟芬那酸 Flufenamic acid 530-78-9
產品規格: 10G 50g
單價: 面議
起訂: 50 g
供貨總量: 1000 g
發貨期限: 自買家付款之日起 3 天內發貨
所在地: 上海
有效期至: 長期有效
最后更新: 2024-12-21 09:43
瀏覽次數: 597
 
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Flufenamic acid

Description Flufenamic acid is a COX-inhibiting non-steroidal anti-inflammatory drug (NSAID) that exhibits neuromodulatory, anti-inflammatory, antipyretic, analgesic, and antiepileptic/anticonvulsant activities. Flufenamic inhibits voltage-gated Na+ channels, transient receptor potential canonical 3 (TRPC3) channels, and transient receptor potential melastatin-like 2 (TRPM2) channels and potentiates TREK1 (KCNK2) channel activity. In vitro, flufenamic acid decreases glutamatergic excitatory activity and neuronal excitability.
Specifications
Cas No. 530-78-9
Product ID F4483
Product Name Flufenamic acid 氟芬那酸 分析標準品
Chemical Name 2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid
Synonym Achless; Ansatin; Arlef; Fullsafe; Parlef; Sastridex; Tecramine
Formula 分子式 C14H10F3NO2
Formula Wt. 分子量 281.23
Melting Point 125oC
Purity ≥97% 純度
Solubility Soluble in 4 parts of ethanol. Soluble in DMSO to 100 mM and in ethanol to 100 mM
Store Temp Ambient
References Xie YF, Zhou F. TRPC3 channel mediates excitation of striatal cholinergic interneurons. Neurol Sci. 2014 May 21. [Epub ahead of print]. PMID: 24844791.

Veale EL, Al-Moubarak E, Bajaria N, et al. Influence of the N terminus on the biophysical properties and pharmacology of TREK1 potassium channels. Mol Pharmacol. 2014 May;85(5):671-81. PMID: 24509840.

Nazrolu M, zgül C, elik , et al. Aminoethoxydiphenyl borate and flufenamic acid inhibit Ca2+ influx through TRPM2 channels in rat dorsal root ganglion neurons activated by ADP-ribose and rotenone. J Membr Biol. 2011 May;241(2):69-75. PMID: 21509529.

Yau HJ, Baranauskas G, Martina M. Flufenamic acid decreases neuronal excitability through modulation of voltage-gated sodium channel gating. J Physiol. 2010 Oct 15;588(Pt 20):3869-82. PMID: 20724367.

Fernández M, Lao-Peregrín C, Martín ED. Flufenamic acid suppresses epileptiform activity in hippocampus by reducing excitatory synaptic transmission and neuronal excitability. Epilepsia. 2010 Mar;51(3):384-90. PMID: 19732136.

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