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CAS No. : 259674-19-6
MCE 国际站:TRPM8 antagonist 2
产品活性:TRPM8 antagonist 2 是一种有效的,选择性的 TRPM8 拮抗剂,IC50 值为 0.2 nM,可用于研究神经性疼痛综合症。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling
作用靶点:TRP Channel
In Vitro: TRPM8 antagonist 2 (Compound 14) is a potent and selective TRPM8 antagonist, with an IC50 of 0.2 nM, used in the research of neuropathic pain syndromes. TRPM8 antagonist 2 potently inhibits menthol-induced increase in intracellular Ca2+ levels in Ca2+ fluorimetric assays in HEK293 cells stably expressing the rat isoform of TRPM8 channels (IC50, 40 nM).
In Vivo: TRPM8 antagonist 2 (1, 10, and 30 mg/kg, s.c.) shows a marked, dose-dependent antinociceptive activity, and inhibits wet-dog shakes (WDS)-like cold hypersensitivity in mice by 63% at 30 mg/kg. In addition, TRPM8 antagonist 2 (0.1 and 1 μg, s.c.) attenuates Oxaliplatin (OXP)-induced cold allodynia in mice.
相关产品:Bioactive Compound Library Plus | Membrane Transporter/Ion Channel Compound Library | Neuronal Signaling Compound Library | Peptidomimetic Library | Mechanoreceptors Compound Library | Pain-Related Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Highly Selective Inhibitors Library | Bisandrographolide C | TRPV1 activator-2 | SB-705498 | AMTB hydrochloride | ABT-239 | AS1269574 | Tivanisiran | RN-1747 | CEDAEVFKDSMVPGEK | Asivatrep | TRPV4 agonist-1 | GsMTx4 TFA | TRPC3/6-IN-2 | SET2 | (E)-4-Oxo-2-nonenal | 1-Stearoyl-2-arachidonoyl-sn-glycerol | Podocarpic acid | M8-B | Pregnenolone monosulfate sodium | TRPC5 modulator-1 | Capsiate | Diisopropyl adipate | FEMA 4809 | Capsazepine | JT010 | Umbellulone | ML-SI1 | TRPC5-IN-4 | EIPA hydrochloride | GSK2193874
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货号: HY-112430
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