Chemical Structure : DDL-920
CAS No.: 1236105-84-2
货号: PC-22875Not For Human Use, Lab Use Only.
DDL-920 is a potent, selective and brain permeable negative allosteric modulator (NAM) of the γ-aminobutyric acid type A receptors (GABARs), inhibits parvalbumin (PV) expressing interneurons (PV+INs) and consequently enhances γ-oscillations both in vitro and in vivo.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥2880 | In stock | |
5 mg | ¥4780 | In stock | |
10 mg | ¥7580 | In stock | |
25 mg | Get quote | ||
100 mg | Get quote |
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DDL-920 is a potent, selective and brain permeable negative allosteric modulator (NAM) of the γ-aminobutyric acid type A receptors (GABAARs), inhibits parvalbumin (PV) expressing interneurons (PV+INs) and consequently enhances γ-oscillations both in vitro and in vivo.
DDL-920 ( 1 nM) increases the power of the γ-oscillations, blocks >75% of tonic inhibition of PV+INs with only a negligible effect on their phasic inhibition in vitro.
DDL-920 increases γ-oscillations and improves cognition/memory in a mouse model of Alzheimer's disease (AD).
DDL-920 (10 mg/kg, oral) restored the cognitive/memory impairments of 3- to 4-mo-old AD model mice as measured by their performance in the Barnes maze.
分子量 | 307.40 | |
分子式 | C19H21N3O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
3-(naphthalen-2-ylmethyl)-4-(piperidin-4-yl)-1H-pyrazol-1-ol |
1. Wei X, et al. Proc Natl Acad Sci U S A. 2024 Aug 13;121(33):e2400420121.
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