GABA Receptor


GABA receptors are a class of receptors that respond to the neurotransmitter gamma-aminobutyric acid (GABA), the chief inhibitory compound in the mature vertebrate central nervous system. GABA receptors influence cognition by coordinating with glutamatergic processes. There are two classes of GABA receptors: GABAA and GABAB. GABAA receptors are ligand-gated ion channels; whereas GABAB receptors are G protein-coupled receptors, also called metabotropic receptors. A subclass of ionotropic GABA receptors, insensitive to typical allosteric modulators of GABAA receptor channels such as benzodiazepines and barbiturates, designated GABAС receptor.
  • NU7026 EY1404

    NU7026是一种有效的DNA-PK抑制剂,IC50为0.23 μM,作用于DNA-PK比作用于PI3K选择性高60倍,抑制ATM和ATR活性。

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  • Lovastatin EY0850

    Lovastatin (洛伐他汀) 是高效HMG-CoA还原酶抑制剂,IC50为3.4 nM,有降血脂作用。

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  • Simvastatin EY0506

    Simvastatin (Zocor)是HMG-CoA还原酶的竞争性抑制剂,Ki为0.1-0.2 nM。

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  • Fluvastatin Sodium EY0440

    Fluvastatin sodium (XU62-320) is a potent, water-soluble inhibitor of HMG-CoA reductase, widely used as a cholesterol- lowering drug. Fluvastatin sodium 是HMG-CoA还原酶竞争性抑制剂。

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  • Pravastatin sodium EY0269

    Pravastatin sodium, a hydrophilic inhibitor, inhibits HMG-CoA reductase resulting in the reduction of cholesterol synthesis. Pravastatin sodium是HMG-CoA还原酶抑制剂,对甾醇合成的IC50为5.6 μM。

    More
  • NU7026 EY1404

    NU7026是一种有效的DNA-PK抑制剂,IC50为0.23 μM,作用于DNA-PK比作用于PI3K选择性高60倍,抑制ATM和ATR活性。

    More
  • Lovastatin EY0850

    Lovastatin (洛伐他汀) 是高效HMG-CoA还原酶抑制剂,IC50为3.4 nM,有降血脂作用。

    More
  • Simvastatin EY0506

    Simvastatin (Zocor)是HMG-CoA还原酶的竞争性抑制剂,Ki为0.1-0.2 nM。

    More
  • Fluvastatin Sodium EY0440

    Fluvastatin sodium (XU62-320) is a potent, water-soluble inhibitor of HMG-CoA reductase, widely used as a cholesterol- lowering drug. Fluvastatin sodium 是HMG-CoA还原酶竞争性抑制剂。

    More
  • Pravastatin sodium EY0269

    Pravastatin sodium, a hydrophilic inhibitor, inhibits HMG-CoA reductase resulting in the reduction of cholesterol synthesis. Pravastatin sodium是HMG-CoA还原酶抑制剂,对甾醇合成的IC50为5.6 μM。

    More
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