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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-GABA Receptor-DDL-920
DDL-920

Chemical Structure : DDL-920

CAS No.: 1236105-84-2

DDL-920 (DDL920)

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.

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2 mg ¥2880 In stock
5 mg ¥4780 In stock
10 mg ¥7580 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

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.

物理化学性质&存储条件

分子量 307.40
分子式 C19H21N3O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-(naphthalen-2-ylmethyl)-4-(piperidin-4-yl)-1H-pyrazol-1-ol

参考文献

1. Wei X, et al. Proc Natl Acad Sci U S A. 2024 Aug 13;121(33):e2400420121.

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