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CCG215022

Catalog No.GC19090

CCG215022는 GRK2, GRK5 및 GRK1에 대해 IC50이 각각 0.15±0.07μM, 0.38±0.06μM 및 3.9±1μM인 G 단백질 결합 수용체 키나제(GRK) 억제제입니다.

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CCG215022 Chemical Structure

Cas No.: 1813527-81-9

Size 가격 재고 수량
1mg
US$94.00
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5mg
US$235.00
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10mg
US$335.00
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50mg
US$1,004.00
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100mg
US$1,406.00
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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

CCG215022 is a G protein-coupled receptor kinases (GRKs) inhibitor with IC50s of 0.15±0.07 uM, 0.38±0.06 uM and 3.9±1 uM for GRK2, GRK5 and GRK1, respectively.

CCG215022 has nanomolar potency against both GRK2 and GRK5 and is at least 20-fold more potent than Paroxetine. In the course of a GRK2 structure-based drug design campaign, CCG215022 exhibits nanomolar IC50 values against both GRK2 and GRK5 and good selectivity against other closely related kinases such as GRK1 and PKA. Treatment of murine cardiomyocytes with CCG215022 results in significantly increases contractility at 20-fold lower concentrations than Paroxetine, an inhibitor with more modest selectivity for GRK2[1].

References:
[1]. Homan KT, et al. Crystal Structure of G Protein-coupled Receptor Kinase 5 in Complex with a Rationally DesignedInhibitor. J Biol Chem. 2015 Aug 21;290(34):20649-59.

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