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Submit ReviewSAR 7334 is a potent TRPC6 inhibitor (IC50 values are 9.5, 226 and 282 nM for TRPC6, TRPC7 and TRPC3-mediated Ca2+ influx). Exhibits no significant activity at TRPC4 and TRPC5 channels. Suppresses TRPC6-dependent acute hypoxic pulmonary vasoconstriction (HPV) in the isolated perfused mouse lung. Orally bioavailable.
分子量 | 440.79 |
公式 | C21H22ClN3O.2HCl |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1333207-63-8 |
PubChem ID | 78357800 |
InChI Key | LFMYIKNZNTZSJX-IQJQELQDSA-N |
Smiles | N[C@@H]1CCCN([C@@H]2CC3=CC=CC=C3[C@H]2OC4=C(C=C(C#N)C=C4)Cl)C1.Cl.Cl |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
water | 44.08 | 100 | |
DMSO | 44.08 | 100 |
以下数据基于产品分子量 440.79。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.27 mL | 11.34 mL | 22.69 mL |
5 mM | 0.45 mL | 2.27 mL | 4.54 mL |
10 mM | 0.23 mL | 1.13 mL | 2.27 mL |
50 mM | 0.05 mL | 0.23 mL | 0.45 mL |
参考文献是支持产品生物活性的出版物。
Maier et al (2015) Discovery and pharmacological characterization of a novel potent inhibitor of diacylglycerol-sensitive TRPC cation channels. Br.J.Pharmacol. 172 3650 PMID: 25847402
If you know of a relevant reference for SAR 7334, please let us know.
关键词: SAR 7334, SAR 7334 supplier, SAR7334, potent, transient, receptor, potential, canonical, channel, TRPC6, inhibitors, inhibits, orally, bioavailable, hypoxic, pulmonary, vasoconstriction, hpv, TRPC, 5831, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 SAR 7334 的部分引用包括:
Vladislav et al (2020) Role of opioid signaling in kidney damage during the development of salt-induced hypertension. Life Sci Alliance 3 PMID: 33046522
Orie T et al (2020) Sites of Circadian Clock Neuron Plasticity Mediate Sensory Integration and Entrainment. Curr Biol 30 2225-2237.e5 PMID: 32386535
Gertjan et al (2021) Gut bacteria-derived 5-hydroxyindole is a potent stimulant of intestinal motility via its action on L-type calcium channels. PLoS Biol 19 e3001070 PMID: 33481771
Xiaoqiang et al (2019) The activity of transient receptor potential channel C-6 modulates the differentiation of fat cells. FASEB J 33 6526-6538 PMID: 30785766
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