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
(479)
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CDK1
(179)
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CDK2
(294)
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CDK3
(21)
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CDK4
(222)
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CDK5
(95)
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CDK6
(168)
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CDK7
(114)
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CDK8
(54)
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CDK9
(198)
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CDK11
(7)
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CDK12
(49)
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CDK13
(25)
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CDK14
(6)
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CDK16
(8)
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CDK19
(24)
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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
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CDK Agonists
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CDK Antagonists
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CDK Activators
(15)
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CDK Modulators
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CDK Degraders
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CDK Controls
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CDK Substrate
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CDK Ligands
(15)
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Cyclin-Dependent Kinases (CDKs) Proteins
(81)
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Cyclin Dependent Kinase 1 (CDK1) Proteins
(9)
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Cyclin-Dependent Kinase 2 (CDK2) Proteins
(11)
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Cyclin-Dependent Kinase 3 (CDK3) Proteins
(6)
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Cyclin-Dependent Kinase 4 (CDK4) Proteins
(5)
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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 (1293)
Related Products (1293)
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Recombinant Proteins (82)
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Antibodies (42)
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CDK Isoform Comparison
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CDK7-IN-12
0 ImagesCat. No.: HY-144175CAS No.: 2750638-94-7CDK7-IN-12 is a potent inhibitor of CDK7. CDK7-IN-12 plays a key role in transcriptional regulation and cell cycle regulation. CDK7-IN-12 effectively inhibit malignant tumor proliferation in vitro and in vivo. CDK7-IN-12 has the potential for the research of cancer disease (extracted from patent WO2021249417A1, compound 43). -
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- CDK2-IN-43
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- CDK12/13 ligand 2
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CDK2-IN-36
0 ImagesCat. No.: HY-170441CAS No.: 3054692-45-1CDK2-IN-36 (compound1) is a CDK2 inhibitor with anticancer activity. -
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CDK12/13-IN-2
0 ImagesCat. No.: HY-173042CAS No.: 3076450-41-1 -
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Aristolochic acid D (Standard)
0 ImagesCat. No.: HY-N1465RCAS No.: 17413-38-6Synonyms: Aristolochic acid-IVa (Standard)Aristolochic acid D (Standard) (Aristolochic acid-IVa (Standard)) is the analytical standard of Aristolochic acid D (HY-N1465). This product is intended for research and analytical applications. Aristolochic acid D (Aristolochic acid-IVa) is an orally active PDE2 (IC50: 4.673 μM) and CDK2 (IC50: 25 μM) inhibitor that can be isolated from Aristolochia indica L. Aristolochic acid D exhibits anti-inflammatory activity and is non-carcinogenic and non-nephrotoxic. Aristolochic acid D can be used in the research of inflammation and tumor-related diseases. -
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ARUK2010489
0 ImagesCat. No.: HY-178171ARUK2010489 (Compound 23) is a potent, selective and brain-penetrant NUAK1 inhibitor with a pIC50 of 8.7. ARUK2010489 also inhibits CDK2, CDK4 and CDK6 activity, with inhibitory rate of 7%, 39% and 26% at 1 μM. ARUK2010489 can be used for the research of neurological disease, such as Alzheimer’s disease (AD). -
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CDK2-IN-46
0 ImagesCat. No.: HY-176174SCAS No.: 2498658-21-0 -
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CDK2-IN-18
0 ImagesCat. No.: HY-155602CAS No.: 364735-73-9CDK2-IN-18 (compound 8q) is a potent inhibitor of CDK2/E and CDK4/D1, with IC50s of 8 nM and 46 nM, respectively. CDK2-IN-18 inhibits the proliferation of tumor cells. -
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Cdk9 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02402 -
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- CDK2/9-IN-1
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EGFR/CDK2-IN-5
0 ImagesCat. No.: HY-180242EGFR/CDK2-IN-5 is a potent dual EGFR and CDK2 inhibitor with IC50s of 17.30 and 212.10 nM, respectively. EGFR/CDK2-IN-5 also inhibits EGFRT790M with an IC50 of 123.8 nM. EGFR/CDK2-IN-5 exhibits potent anticancer activity. EGFR/CDK2-IN-5 induces G1 and S cell cycle arrest and apoptosis, accompanied by increased levels of caspase-3/9 and Bax, as well as decreased Bcl-2 levels. EGFR/CDK2-IN-5 can be used for the research of cancers, such as lung cancer, breast cancer, and leukemia. -
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CDK-IN-15
0 ImagesCat. No.: HY-168134CAS No.: 3036232-03-5CDK-IN-15 (Compound 456) is a potent Cyclin A inhibitor, with an IC50 of 0.14 μM. -
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Cdk2 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS02375 -
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CDK7-IN-20
0 ImagesCat. No.: HY-151878CAS No.: 3034210-97-1 -
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Tacaciclib
0 ImagesTacaciclib is a CDK inhibitor, antineoplastic effect. -
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CDK9 ligand 4
0 ImagesCat. No.: HY-181275CAS No.: 2609749-29-1CDK9 ligand 4 is a CDK9 ligand. As a ligand for target protein for PROTAC (Ligands for Target Protein for PROTAC), CDK9 ligand 4 serves for the development and design of PROTAC CDK9 degraders, such as PROTAC CDK9 degrader-12 (HY-181231). CDK9 ligand 4 is applicable to the research of HIV-1 infection. -
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CDK9 autophagic degrader 1
0 ImagesCat. No.: HY-168896CAS No.: 3066836-42-5CDK9 autophagic degrader 1 (Compound 28) is a ATTEC degrader that can be used to degrade CDK9 and also affects the levels of the associated Cyclin T1. CDK9 autophagic degrader 1 shows over 80% CDK9 inhibition rate at 100 nM. ( Pink: LC3B ligand (HY-168897); Black: linker (HY-W017758); Blue: target protein ligand (HY-10008); linker + target protein ligand (HY-168898)) -
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CDK8-IN-7
0 ImagesCat. No.: HY-147717CAS No.: 2415156-30-6CDK8-IN-7 (compound 12) is a potent and selective cyclin-dependent kinase 8 (CDK8) inhibitor with an Kd of 3.5 nM. CDK8-IN-7 shows cytotoxicity for MOLM-13, OCI-AML3, MV4-11, NRK and H9c2 cells with IC50s of 5.9, 4.8, 5.4, 16.2, 12.5-25 µM, respectively. CDK8-IN-7 has the potential for the research of AML-cancer. -
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ZNL-02-096
0 ImagesCat. No.: HY-208742CAS No.: 2414418-56-5ZNL-02-096 is a selective Wee1 PROTAC degrader. ZNL-02-096 binds to CRBN and Wee1 to form a ternary complex, inducing CRBN- and proteasome-dependent ubiquitination and proteasomal degradation of Wee1. ZNL-02-096 inhibits recombinant PLK1 with an IC50 of 102 nM, but does not induce its degradation in cells. ZNL-02-096 induces G2/M phase arrest, Apoptosis, transient integrated stress response, upregulation of ATF4, and phosphorylation of GCN2. ZNL-02-096 reduces Tyr15 phosphorylation of CDK1. ZNL-02-096 can be used in research related to ovarian cancer, acute lymphoblastic leukemia, triple-negative breast cancer, multiple myeloma, and pancreatic ductal adenocarcinoma. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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