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Submit ReviewOrg 24598 is a potent and selective inhibitor of the glial glycine transporter GlyT1b (IC50 = 6.9 nM). Displays negligible activity at GlyT-2, adrenoreceptors, dopamine, 5HT receptors and noradrenaline, dopamine, 5HT and GABA transporters (pIC50 < 4). Active in vivo.
分子量 | 367.36 |
公式 | C19H20F3NO3 |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 372198-97-5 |
PubChem ID | 5311285 |
InChI Key | KZWQAWBTWNPFPW-QGZVFWFLSA-N |
Smiles | CN(CC(O)=O)CC[C@@H](OC2=CC=C(C(F)(F)F)C=C2)C1=CC=CC=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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 36.74 | 100 |
以下数据基于产品分子量 367.36。 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 | 2.72 mL | 13.61 mL | 27.22 mL |
5 mM | 0.54 mL | 2.72 mL | 5.44 mL |
10 mM | 0.27 mL | 1.36 mL | 2.72 mL |
50 mM | 0.05 mL | 0.27 mL | 0.54 mL |
参考文献是支持产品生物活性的出版物。
Chue et al (2013) Glycine reuptake inhibition as a new therapeutic approach in schizophrenia: focus on the glycine transporter 1 (GlyT1). Curr.Pharm.Des. 19 1311 PMID: 23194655
Brown et al (2001) Discovery and SAR of org 24598-a selective glycine uptake inhibitor. Bioorg.Med.Chem.Lett. 11 2007 PMID: 11454468
Williams et al (2003) Development of a scintillation proximity assay for analysis of Na+/Cl- -dependent neurotransmitter transporter activity. Anal. Biochem. 321 31 PMID: 12963052
If you know of a relevant reference for Org 24598, please let us know.
关键词: Org 24598, Org 24598 supplier, Org24598, glial, glycine, transporters, glyt1, inhibitors, inhibits, Glycine, Transporters, 4447, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Org 24598 的部分引用包括:
Jaekwang et al (2020) The molecular mechanism of synaptic activity-induced astrocytic volume transient. J Physiol 598 4555-4572 PMID: 32706443
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