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Protein Kinase A (PKA)

Protein Kinase A (PKA)

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CCG215022

Catalog No. A16189
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GRK2/5 抑制剂

CCG215022是有效的GRK2和GRK5抑制剂。CCG215022对GRK2和GRK5均表现出纳摩尔IC50值，对其他紧密相关的激酶（如GRK1和PKA）具有良好的选择性。了解更多

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cGMP Dependent Kinase Inhibitor Peptid

Catalog No. A16052
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PKG/PKA 抑制剂

cGMP Dependent Kinase Inhibitor Peptid是一种特定的cGKI（环GMP依赖性蛋白激酶）抑制剂。数据表明，它不阻断完整组蛋白的环状GMP依赖性蛋白激酶磷酸化，已被用于研究恶性疟原虫。了解更多

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PKI 14-22 amide, myristoylated

Catalog No. A16031
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PKA 抑制剂

PKI 14-22 amide, myristoylated是有用的热稳定的cAMP依赖性蛋白激酶抑制剂。这通常用于体外研究细胞系统中的PKA。了解更多

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- Dao-Lai Zhang, .et al. Gq activity- and β-arrestin-1 scaffolding-mediated ADGRG2/CFTR coupling are required for male fertility, eLife, 2018, 7: e33432 PMID: 29393851
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KT 5720

Catalog No. A16016
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PKA 抑制剂

KT5720 是一种能透过细胞的、有效的、特异性的、可逆的、ATP 竞争性的蛋白酶 K (PKA) 的抑制剂，其 Ki 值为 60 nM。了解更多

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AT7867 2HCl

Catalog No. A15006
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Akt 抑制剂

AT7867 dihydrochloride是一种有效的ATP竞争性Akt1/2/3和p70S6K/PKA抑制剂，IC50分别为32 nM/17 nM/47 nM和85 nM/20 nM，在AGC激酶家族之外几乎没有活性。了解更多

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NH125

Catalog No. A14307
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eEF-2 抑制剂

NH125是选择性eEF-2激酶抑制剂。了解更多

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AT13148

Catalog No. A12464
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multi-AGC kinase 抑制剂

AT13148是一种新型多AGC激酶抑制剂，具有强大的药效和抗肿瘤活性，与其他AKT抑制剂相比，具有独特的作用机理。了解更多

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H 89 2HCl

Catalog No. A11935
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PKA 抑制剂

H 89 dihydrochloride是一种可渗透细胞的，选择性的，可逆的，具有ATP竞争性的有效蛋白激酶抑制剂。了解更多

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- Guo Q, .et al. Antineuropathic pain actions of Wu-tou decoction resulted from the increase of neurotrophic factor and decrease of CCR5 expression in primary rat glial cells, Biomed Pharmacother, 2020, Mar;123:109812 PMID: 31945696
- Y Kaibori, .et al. EphA2 phosphorylation at Ser897 by the Cdk1/MEK/ERK/RSK pathway regulates M-phase progression via maintenance of cortical rigidity, the FASEB Journal, 2019, Jan 22:fj201801519RR PMID: 30668924
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Daphnetin

Catalog No. A10286
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EGFR, PKA,PKC 抑制剂

Daphnetin是一种香豆素类似物，可作为几种蛋白激酶的抑制剂。它在体外抑制EGFR激酶（IC50 = 7.67 ?M），PKA（IC50 = 9.33 ?M）和PKC（IC50 = 25 ?M）。蜂胶对EGFR激酶的抑制作用与ATP竞争，对肽底物没有竞争性。还可以用作有效的抗氧化剂和抗疟疾剂。了解更多

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A-674563

Catalog No. A11034
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Akt 抑制剂

A-674563是一种B/Akt抑制剂，IC50为14 nM，并且还显示出对PKA和CDK2的抑制活性，IC50分别为16和46 nM。了解更多

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- Kobayashi T, .et al. A-674563 increases chondrocyte marker expression in cultured chondrocytes by inhibiting Sox9 degradation, Biochem Biophys Res Commun, 2018, Jan 1;495(1):1468-1475 PMID: 29196261
- Lin Xu, .et al. Concurrent targeting Akt and sphingosine kinase 1 by A-674563 in acute myeloid leukemia cells, Biochem Biophys Res Commun, 2016, Apr 15;472(4):662-8 PMID: 26920060
- Zou Y, .et al. Pre-clinical assessment of A-674563 as an anti-melanoma agent, Biochem Biophys Res Commun, 2016, Aug 12;477(1):1-8 PMID: 26970307
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PKA inhibitor fragment (6-22) amide

Catalog No. A14868
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PKA 抑制剂

PKA inhibitor fragment (6-22) amide是一种合成肽，可作为蛋白激酶抑制剂。了解更多

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cAMPS-Rp, triethylammonium salt

Catalog No. A16028
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reversible PKA 抑制剂

cAMPS-Rp,triethylammonium salt是PKA（蛋白激酶A）（Ki = 11 uM）的细胞渗透性和可逆抑制剂.Rp-cAMPS耐磷酸二酯酶水解，相对于ATP不具竞争力。了解更多

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A-3 Hydrochloride

Catalog No. A13584
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PKA, PKG, Casein Kinase I and II 抑制剂

A-3 Hydrochloride是PKA（cAMP依赖性蛋白激酶，Ki =4.3μM）和cGMP依赖性蛋白激酶，Ki =3.8μM，PKC（蛋白激酶C，Ki =47μM），酪蛋白激酶I和II的抑制剂，和MLCK（肌球蛋白轻链激酶）（Ki =7.4μM）。了解更多

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