RN 1747

Discontinued Product

3745 has been discontinued.

View all TRPV Channels products.
说明: Selective TRPV4 agonist
化学名: 1-(4-Chloro-2-nitrophenyl)sulfonyl-4-benzylpiperazine
纯度: ≥98% (HPLC)
说明书
引用文献 (4)
评论

生物活性 for RN 1747

RN 1747 is a selective TRPV4 agonist (EC50 values are 0.77, 4.0 and 4.1 μM for hTRPV4, mTRPV4 and rTRPV4 respectively). Displays selectivity over other TRP channels (EC50 values are 0.77, >30, >30 and >100 μM for TRPV4, TRPM8, TRPV3 and TRPV1 receptors respectively). Also antagonizes TRPM8 at relevant concentrations (IC50 = 4 μM).

化合物库 for RN 1747

RN 1747 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for RN 1747

分子量 395.87
公式 C17H18ClN3O4S
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 1024448-59-6
PubChem ID 5068295
InChI Key ZNLVYSJQUMALEO-UHFFFAOYSA-N
Smiles ClC1=CC=C(S(N2CCN(CC3=CC=CC=C3)CC2)(=O)=O)C([N+]([O-])=O)=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

产品说明书 for RN 1747

分析证书/产品说明书
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参考文献 for RN 1747

参考文献是支持产品生物活性的出版物。

Vincent et al (2009) Identification and characterization of novel TRPV4 modulators. Biochem.Biophys.Res.Comms. 389 490 PMID: 19737537

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关键词: RN 1747, RN 1747 supplier, RN1747, selective, TRPV4, agonists, transient, receptors, potential, channels, vanilloid, TRPV, 3745, Tocris Bioscience

4 篇 RN 1747 的引用文献

引用文献是使用了 Tocris 产品的出版物。 RN 1747 的部分引用包括:

Christopher D et al (2020) Dysregulation of TRPV4, eNOS and caveolin-1 contribute to endothelial dysfunction in the streptozotocin rat model of diabetes. Eur J Pharmacol 888 173441 PMID: 32810492

Shi et al (2015) Alterations in serotonin, transient receptor potential channels and protease-activated receptors in rats with irritable bowel syndrome attenuated by Shugan decoction. Am J Physiol Renal Physiol 21 4852 PMID: 25944998

Vizin et al (2015) TRPV4 activates autonomic and behavioural warmth-defence responses in Wistar rats. Acta Physiol 214 275 PMID: 25739906

Shabir et al (2013) Functional expression of purinergic P2 receptors and transient receptor potential channels by the human urothelium. World J Gastroenterol 305 F396 PMID: 23720349


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