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CDK Related Products (486)
Related Products (486)
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(E/Z)-THZ1 dihydrochloride
0 ImagesCat. No.: HY-80013BCAS No.: 2095433-94-4(E/Z)-THZ1 dihydrochloride is a selective inhibitor of CDK7 with an IC50 of 3.2 nM. (E/Z)-THZ1 dihydrochloride has antiproliferative effect. -
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CDK2 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02374 -
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AT7519 Hydrochloride (Standard)
0 ImagesAT7519 (Hydrochloride) (Standard) is the analytical standard of AT7519 (Hydrochloride). This product is intended for research and analytical applications. AT7519 Hydrochloride is a potent inhibitor of CDKs, with IC50s of 210, 47, 100, 13, 170, and <10 nM for CDK1, CDK2, CDK4 to CDK6, and CDK9, respectively. -
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(S)-(-)-O-Demethylbuchenavianine
0 ImagesCat. No.: HY-N12625ACAS No.: 91147-18-1 -
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CDK4-IN-1
0 ImagesCat. No.: HY-15612CAS No.: 1256963-02-6CDK4 inhibitor is a novel and specific CDK4/Cyclin D1 inhibitor with an IC50 of 10 nM; 1500 and 500 fold than CDK1/Cyclin B (IC50>15 uM) and CDK2/Cyclin A (IC50=5.265 uM) respectively. -
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1-Stearoyl-2-Adrenoyl-sn-glycero-3-PC
0 ImagesSynonyms: PC(18:0/22:4)1-Stearoyl-2-Adrenoyl-sn-glycero-3-PC (PC(18:0/22:4)) is an inhibitor of cyclin-dependent kinases (CDKs). 1-Stearoyl-2-Adrenoyl-sn-glycero-3-PC induces apoptosis and inhibits the growth of various cancer cell lines. -
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Ribociclib succinate (Standard)
0 ImagesSynonyms: LEE011 succinate (Standard)Ribociclib succinate (Standard) is the analytical standard of Ribociclib succinate. This product is intended for research and analytical applications. Ribociclib succinate (LEE011 succinate) is a highly specific CDK4/6 inhibitor with IC50 values of 10 nM and 39 nM, respectively, and is over 1,000-fold less potent against the cyclin B/CDK1 complex. -
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Cdc7-IN-4
0 ImagesCat. No.: HY-130516CAS No.: 1402059-21-5 -
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Tibremciclib
0 ImagesCat. No.: HY-156646CAS No.: 2397678-18-9Synonyms: BPI-16350Tibremciclib is a CDK4 inhibitor with antineoplastic activity. -
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Fovinaciclibum
0 ImagesCat. No.: HY-159535CAS No.: 2146171-49-3Synonyms: FovinaciclibFovinaciclib is an orally active CDK (CDK4/6) inhibitor with antitumor activity. -
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rel-AZ5576
0 ImagesCat. No.: HY-111537CAS No.: 1333468-05-5rel-AZ5576 is a selective CDK9 inhibitor with the activity of downregulating Mcl-1 and MYC mRNA transcription and protein expression in diffuse large B-cell lymphoma by inhibiting CDK9, promoting MYC protein turnover, reducing MYC phosphorylation on the stable Ser62 residue and downregulating MYC transcriptional targets, inhibiting the growth of diffuse large B-cell lymphoma cell lines in vitro and in vivo and independent of the cell origin. -
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CDK9-IN-29
0 ImagesCat. No.: HY-149641CAS No.: 2737262-24-5 -
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Cdc7-IN-3
0 ImagesCat. No.: HY-130515CAS No.: 1402057-87-7 -
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- Cdc7-IN-7
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QR-6401
0 ImagesCat. No.: HY-153221CAS No.: 2845096-18-4QR-6401 is an orally active and selective macrocyclic CDK2 inhibitor with IC50 values of 0.37, 10, 22, 34 and 45 nM for CDK2/E1, CDK9/T1, CDK1/A2, CDK6/D3 and CDK4/D1, respectively. QR-6401 has potent antitumor activity in an OVCAR3 ovarian cancer xenograft model. QR-6401 has the potential to be used in the study of cancer. -
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CDK-IN-13
0 ImagesCat. No.: HY-157297CAS No.: 3041994-96-8CDK-IN-13 (compound 32E) is a potent and selective inhibitor of CDK12/cyclinK with an IC50 of 3 nM. CDK-IN-13 inhibits the growth of the HER2-positive breast cancer cell lines. -
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AGM-130
0 ImagesCat. No.: HY-114248CAS No.: 1459216-10-4AGM-130 is a cyclin-dependent kinase (CDK) inhibitor. AGM-130 exhibits antitumor activity. -
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- BC13
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CDK3/CycE1 Recombinant Human Active Protein Kinase
0 ImagesCat. No.: HY-E70678CDK3 is a major player driving retinoblastoma (Rb) phosphorylation during the G0/G1 transition and in the early G1 phase of the cell cycle. CDK3 interacts with various transcription factors involved in cell proliferation, differentiation, and transformation driven by the EGFR/Ras signaling pathway. CDK3/CycE1 Recombinant Human Active Protein Kinase is an ortholog of CDK3. -
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CDK8/CycC Recombinant Human Active Protein Kinase
0 ImagesCat. No.: HY-E70690CDK8 modulates the transcriptional output from distinct transcription factors involved in oncogenic control, including the Wnt/β-catenin pathway, Notch, p53, and transforming growth factor β. Abnormal activity ofCDK8 along with its partner protein cyclin C (CycC) is a common feature of many diseases including colorectal cancer. CDK8/CycC Recombinant Human Active Protein Kinase can be used to study the function of CDK8/CycC. -
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