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CAS No. : 956274-94-5
MCE 国际站:Mavatrep
产品活性:Mavatrep (JNJ-39439335) 是一种口服有效的、具有选择性的强效 TRPV1 拮抗剂,对 hTRPV1 通道具有高亲和力 (Ki=6.5 nM)。Mavatrep 能拮抗辣椒素诱导的 Ca2+ 流入,其 IC50 值为4.6 nM。Mavatrep 可用于某些神经病理性疼痛的研究。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling
作用靶点:TRP Channel
In Vitro: Mavatrep (series of decreasing concentrations from 1 μM; 25 min) inhibits capsaicin-induced Ca2+ influx in HEK293 cells expressing TRPV1 channels.
In Vivo: Mavatrep (1, 3, 10, 30 mg/kg; p.o.; single) shows complete reversal of thermal hypersensitivity both in CFA model of inflammatory of pain and (0.1, 0.3, 1, 3, 10 mg/kg) carrageenan model of inflammatory pain.
Mavatrep (10 mg/kg; p.o.; single) exhibits substantial bioavailability in the rat (51%).
相关产品:Clinical Compound Library Plus | Bioactive Compound Library Plus | Membrane Transporter/Ion Channel Compound Library | Neuronal Signaling Compound Library | Clinical Compound Library | Orally Active Compound 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-16935
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