CDK
Cyclin dependent kinase
CDKs (Cyclin-dependent kinases) are serine-threonine kinases first discovered for their role in regulating the cell cycle. They are also involved in regulating transcription, mRNA processing, and the differentiation of nerve cells. CDKs are relatively small proteins, with molecular weights ranging from 34 to 40 kDa, and contain little more than the kinase domain. In fact, yeast cells can proliferate normally when their CDK gene has been replaced with the homologous human gene. By definition, a CDK binds a regulatory protein called a cyclin. Without cyclin, CDK has little kinase activity; only the cyclin-CDK complex is an active kinase.
There are around 20 Cyclin-dependent kinases (CDK1-20) known till date. CDK1, 4 and 5 are involved in cell cycle, and CDK 7, 8, 9 and 11 are associated with transcription.
CDK levels remain relatively constant throughout the cell cycle and most regulation is post-translational. Most knowledge of CDK structure and function is based on CDKs of S. pombe (Cdc2), S. cerevisia (CDC28), and vertebrates (CDC2 and CDK2). The four major mechanisms of CDK regulation are cyclin binding, CAK phosphorylation, regulatory inhibitory phosphorylation, and binding of CDK inhibitory subunits (CKIs).
CDK Isoform Specific Products
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CDK
(486)
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CDK1
(198)
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CDK2
(316)
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CDK3
(28)
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CDK4
(236)
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CDK5
(98)
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CDK6
(179)
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CDK7
(119)
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CDK8
(57)
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CDK9
(206)
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CDK11
(9)
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CDK12
(54)
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CDK13
(28)
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CDK14
(6)
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CDK16
(8)
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CDK19
(25)
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CDC
(21)
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CLK
(31)
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Pho85
(1)
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CDK10
(1)
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CDK15
(1)
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CDK17
(2)
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CDK18
(1)
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CDK20
(1)
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PITSLRE
(1)
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All Product Categories
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CDK Inhibitors
(1088)
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CDK Agonists
(3)
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CDK Antagonists
(2)
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CDK Activators
(18)
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CDK Modulators
(15)
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CDK Degraders
(95)
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CDK Controls
(4)
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CDK Substrate
(1)
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CDK Ligands
(16)
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Cyclin-Dependent Kinases (CDKs) Proteins
(80)
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Cyclin Dependent Kinase 1 (CDK1) Proteins
(9)
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Cyclin-Dependent Kinase 2 (CDK2) Proteins
(12)
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Cyclin-Dependent Kinase 3 (CDK3) Proteins
(6)
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Cyclin-Dependent Kinase 4 (CDK4) Proteins
(4)
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Cyclin-Dependent Kinase 5 (CDK5) Proteins
(5)
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Cyclin-Dependent Kinase 6 (CDK6) Proteins
(6)
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Cyclin-Dependent Kinase 7 (CDK7) Proteins
(4)
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CDK Related Products (1364)
Related Products (1364)
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Recombinant Proteins (82)
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Antibodies (42)
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CDK Isoform Comparison
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EGFR/HER2/CDK9-IN-2
0 ImagesCat. No.: HY-147797CAS No.: 1180924-34-8 -
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Cdk16 Rat Pre-designed siRNA Set A
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CDK4/CycD2 Recombinant Human Active Protein Kinase
0 ImagesCat. No.: HY-E70682CDK4 has a well-established role in cell-cycle controland CDK4-cyclin complexes are commonly deregulated in tumorigenesis. CDK4/CycD2 Recombinant Human Active Protein Kinase is an ortholog of CDK4. -
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CDK2-IN-56
0 ImagesCat. No.: HY-10793CAS No.: 802536-13-6 -
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CDK2-IN-14-d3
0 ImagesCat. No.: HY-151580SCAS No.: 2498658-25-4CDK2-IN-14-d3 is a potent and selective CDK2 inhibitor. CDK2-IN-14-d3 can be used in research of cancer. -
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CDK9 ligand 3
0 ImagesCat. No.: HY-170979CAS No.: 3039540-24-1CDK9 ligand 3 is the ligand for CDK9 and can be used for synthesis of PROTAC degrader PROTAC CDK9 degrader-11 (HY-170978). -
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CDK7-IN-27
0 ImagesCat. No.: HY-162416CAS No.: 3025006-89-4CDK7-IN-27 (Compound 37) is a selective inhibitor for cyclin-dependent kinase 7 (CDK7), with Ki of 3 nM. CDK7-IN-27 arrests the cell cycle at G0/G1 phase. -
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CDK4/6-IN-13
0 ImagesCat. No.: HY-146214CAS No.: 1908454-70-5As a cdk4/6 inhibitor. Compounds 10B and 10C showed low nanomolar activity, ideal antiproliferative activity, excellent metabolic properties and acceptable pharmacokinetics on cdk4/6. -
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UNC10112785
0 ImagesCat. No.: HY-128491CAS No.: 748142-06-5UNC10112785 is a serine/threonine kinase inhibitor with a human GSK-3β IC50 of 0.031 μM, human CDK-2 IC50 of 0.016 μM, and human CDK-4 IC50 of 1.99 μM. UNC10112785 can be used for the research of type 2 diabetes. -
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CDK8 ligand 2
0 ImagesCat. No.: HY-184544CAS No.: 2374703-22-5 -
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Avotaciclib sulfate
0 ImagesCat. No.: HY-137432DCAS No.: 1983984-04-8Synonyms: BEY1107 sulfateAvotaciclib (BEY1107) sulfate is an orally active cyclin-dependent kinase 1 (CDK1) inhibitor. Avotaciclib sulfate can inhibit the proliferation and induce apoptosis of tumor cells. Avotaciclib sulfate can be used in the research of cancer such as pancreatic cancer and lung cancer. -
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MPT0L145
0 ImagesCat. No.: HY-122888CAS No.: 2070837-24-8MPT0L145 is a PIK3C3/FGFR inhibitor, with a Kd value of 0.53 nM for PIK3C3. MPT0L145 decreases the phosphorylation of FGFR1, FGFR3 and their downstream proteins (FRS2, ERK and Akt). MPT0L145 induces G0/G1 cell cycle arrest and decreased protein levels of cyclin E. MPT0L145 promotes mitochondrial dysfunction, ROS production, and DNA damage. MPT0L145 is an autophagy inhibitor. MPT0L145 significantly sensitizes cancer cells to targeted or chemotherapeutic agents. MPT0L145 can be used for cancer research, such as bladder cancer and NSCLC. -
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Cdk12 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02357 -
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Hsp90-IN-42
0 ImagesCat. No.: HY-176279Hsp90-IN-42 is a heat shock protein 90 (Hsp90) inhibitor with an IC50 of 15.65 nM against human targets. Hsp90-IN-42 destabilizes EGFR and inhibits the activation of the EGFR-Akt signaling pathway. Hsp90-IN-42 suppresses the proliferation and migration of cancer cells, induces cell cycle arrest by downregulating CDK12 and CDK13, and triggers mild apoptosis via downregulating Bcl-2 and upregulating Bax. Hsp90-IN-42 inhibits tumor growth in xenograft mouse models. Hsp90-IN-42 can be used in research related to colorectal cancer. -
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- Cdc7-IN-20
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Anticancer agent 298
0 ImagesCat. No.: HY-181116Anticancer agent 298 is a bi-nuclear Cu(II)-hydrazone complexe. Anticancer agent 298 can bind to the CDK-2 active site (PDB ID: 3IG7) via hydrogen bonds with key amino acid residues. Anticancer agent 298 exerts cytotoxic effects against hepatocellular carcinoma cells, and has lower cytotoxicity against normal human embryonic kidney cells. Anticancer agent 298 can be used for the research of hepatocellular carcinoma. -
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5-HT6 inverse agonist 1
0 ImagesCat. No.: HY-168333CAS No.: 2727088-38-05-HT6 inverse agonist 1 (Compound 33) is an antagonist for 5-HT6 receptor with a Ki of 23 nM and a Kb of 6.62 nM. 5-HT6 inverse agonist 1 inhibits the 5-HT6R mediated Cdk5 and mTOR signaling pathway. 5-HT6 inverse agonist 1 reduces tactile hypersensitivity in spinal nerve ligation (SNL)-induced rat model. -
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VMY-1-101
0 ImagesCat. No.: HY-182383CAS No.: 1209002-42-5VMY-1-101 is a fluorescent cyclin-dependent kinase (CDK) inhibitor, with an excitation of 410 nm and emission of 512 nm. VMY-1-101 competitively inhibits ATP binding to CDKs. VMY-1-101 induces G2/M cell cycle arrest in human breast cancer cells. VMY-1-101 induces modest apoptosis in human breast cancer cells. VMY-1-101 blocks proliferation of human breast cancer cells, including multidrug resistance-positive cells, and is not a substrate for p-glycoprotein. VMY-1-101 localizes to the cytoplasm of human breast cancer cells. VMY-1-101 shows increased binding to human breast cancer tissue compared to fluorophore alone. VMY-1-101 can be used for the research of breast cancer. -
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FLT3/CDK4-IN-1
0 ImagesCat. No.: HY-115904CAS No.: 2762296-44-4 -
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VEGFR2-IN-86
0 ImagesCat. No.: HY-182789VEGFR2-IN-86 is a dual VEGFR2/CDK2 inhibitor, with an IC50 of 0.06 μM against VEGFR2 and an IC50 of 0.78 μM against CDK2. VEGFR2-IN-86 induces G-phase cell cycle arrest, reduces colony-forming ability and tumor cell migration capacity, and exerts antiproliferative activity in cancer cells. VEGFR2-IN-86 can be used for the research of breast cancer and prostate cancer. -
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