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15154-5A 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC<sub>50</sub> = 60 nM).
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15154-500A 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC<sub>50</sub> = 60 nM).
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17648-1A cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by selectively blocking cyclin D1/Cdk4 (IC<sub>50</sub> = 0.8 &muM) inhibits HCT116 and NCI-H460 tumor cell growth (IC<sub>50</sub>s 1 cell cycle arrest.
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17648-5A cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by selectively blocking cyclin D1/Cdk4 (IC<sub>50</sub> = 0.8 &muM) inhibits HCT116 and NCI-H460 tumor cell growth (IC<sub>50</sub>s 1 cell cycle arrest.
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17648-500A cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by selectively blocking cyclin D1/Cdk4 (IC<sub>50</sub> = 0.8 &muM) inhibits HCT116 and NCI-H460 tumor cell growth (IC<sub>50</sub>s 1 cell cycle arrest.
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17974-1A cell-permeable triaminopyrimidine that selectively and reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity (IC<sub>50</sub>s = 1.5 and 5.
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17974-10A cell-permeable triaminopyrimidine that selectively and reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity (IC<sub>50</sub>s = 1.5 and 5.
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17974-5A cell-permeable triaminopyrimidine that selectively and reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity (IC<sub>50</sub>s = 1.5 and 5.
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17477-1A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17477-10A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17477-5A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17477-500A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.