Ro 67-7476
目录号 : GC12485A positive allosteric modulator of mGluR1
Cas No.:298690-60-5
Sample solution is provided at 25 µL, 10mM.
Ro 67-7476 is a positive allosteric modulator of mGlu1 receptors. Displays no activity at human mGlu1 receptors. Potentiates glutamate-induced calcium release with EC 50 of 60.1 nM.target: mGlu1 EC 50: 60.1 nM(1) Ro 67-7476 (10 μM) can directly block the GIRK channel (to 67 ± 2% of control). (2) Ro 67-7476 enhance the glutamate-induced current in all chimeric receptors containing the transmembrane (TM) region of rmGlu1a (R1, R1-R5N, R1-R5C, and R5-R1TM) but not in those containing the TM region of rmGlu5a (R5, R5-R1N, R5-R1C, and R1-R5TM.(3) The application of Ro 67-7476 (3 μM) produced no effect alone but resulted in a marked potentiation of the mGlu1 EPSC amplitude.
References:
[1]. Hemstapat K et al. A novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators. Mol Pharmacol. 2006 Aug, 70(2), 616-26
[2]. Knoflach F et al. Positive allosteric modulators of metabotropic glutamate 1 receptor: characterization, mechanism of action, and binding site. Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):13402-7.
Cas No. | 298690-60-5 | SDF | |
化学名 | (S)-2-(4-fluorophenyl)-1-tosylpyrrolidine | ||
Canonical SMILES | FC1=CC=C(C=C1)[C@H](CCC2)N2S(=O)(C3=CC=C(C)C=C3)=O | ||
分子式 | C17H18FNO2S | 分子量 | 319.39 |
溶解度 | DMSO: 30 mg/ml | 储存条件 | Store at -20°C |
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1 mg | 5 mg | 10 mg | |
1 mM | 3.131 mL | 15.6548 mL | 31.3097 mL |
5 mM | 0.6262 mL | 3.131 mL | 6.2619 mL |
10 mM | 0.3131 mL | 1.5655 mL | 3.131 mL |
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% DMSO % % Tween 80 % saline | ||||||||||
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工作液浓度: mg/ml;
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2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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Quality Control & SDS
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- Purity: >99.00%
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