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
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CDK1
(187)
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CDK2
(302)
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CDK3
(28)
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CDK4
(223)
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CDK5
(96)
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CDK6
(168)
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CDK7
(115)
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CDK8
(55)
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CDK9
(200)
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CDK11
(8)
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CDK12
(50)
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CDK13
(25)
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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
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PITSLRE
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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
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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
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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
(12)
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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 (1316)
Related Products (1316)
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Recombinant Proteins (83)
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Antibodies (42)
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CDK Isoform Comparison
- PROTAC CDK9 degrader-2
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Abemaciclib metabolite M2-d6
0 ImagesCat. No.: HY-128669SPurity: 99.90%Synonyms: LSN2839567-d6Abemaciclib metabolite M2-d6 is the deuterium labeled Abemaciclib metabolite M2. Abemaciclib metabolite M2 (LSN2839567) is a metabolite of Abemaciclib, acts as a potent CDK4 and CDK6 inhibitor, with IC50s in the range of 1-3 nM. Anti-cancer activity. -
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- NSC 625987
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- SHR5428
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AG-012986
0 ImagesAG-012986 is a pan-CDK inhibitor with Ki values of 44 nM (CDK1), 9.2 nM (CDK4), 94 nM (CDK2), and IC50 values of 22 nM (CDK5), 4 nM (CDK9). AG-012986 causes apoptosis of T-cells by targeting upstream kinases in the p38 Mitogen-activated protein kinase (MAPK) pathway and impairing cellular survival. AG-012986 induces cell cycle arrest, retinoblastoma protein hypophosphorylation, and reduces Ki-67 expression. AG-012986 exerts antiproliferative activity in tumor cells, demonstrates antitumor efficacy in human xenograft models, and causes retinal and peripheral neurotoxicity, plus immune cell toxicity. AG-012986 can be used for the research of colon carcinoma, non-small cell lung carcinoma, lung carcinoma, breast carcinoma, ovarian tumor, pancreatic carcinoma, osteosarcoma, lymphoma, leukemia, retinotoxicity. -
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- CDK1-IN-2
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DB18
0 ImagesDB18 is a potent and selective inhibitor of CDC2-like kinases (CLKs), with IC50 values in the range of 10-30 nM for CLK1, CLK2 and CLK4. DB18 has anti-tumor activity. -
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- DDO-6079
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CGP-82996
0 ImagesSynonyms: CINK4 -
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- 5-Iodo-indirubin-3'-monoxime
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KH-CB20
0 ImagesKH-CB20, an E/Z mixture, is a potent and selective inhibitor of CLK1 and the closely related isoform CLK4, with an IC50 of 16.5 nM for CLK1. KH-CB20 can also inhibit DYRK1A (IC50=57.8 nM) and CLK3 (IC50=488 nM). -
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Ganoderic acid H
0 ImagesGanoderic acid H is a hydroxylated lanostane-type triterpenoid derived from Ganoderma lucidum with anticancer activity. Ganoderic acid H inhibits the constitutive transactivation activity of AP-1 and NF-κB; it also downregulates the secretion of uPA and the expression of CDK4, and suppresses the growth, adhesion, migration and invasion of cancer cells. Ganoderic acid H inhibits HIV-1 protease in vitro. Ganoderic acid H can be used in studies related to breast cancer and HIV infection. -
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Sulindac sulfone
0 ImagesSulindac sulfone is an orally active metabolite of Sulindac (HY-B0008). Sulindac sulfone activates PPARγ and drives transcriptional induction of SSAT by binding to the PPRE-2 element. Sulindac sulfone induces Apoptosis. Sulindac sulfone negatively regulates the function of VDAC1/2 to inhibit the mTORC1 pathway, reduces Cyclin D1 levels, and induces G1 cell cycle arrest in colon cancer cells. Sulindac sulfone exerts colon cancer preventive effects through a COX-independent mechanism. Sulindac sulfone can be used in research related to colon cancer. -
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Casein Kinase inhibitor A86
0 ImagesCasein Kinase inhibitor A86 is a potent and orally active casein kinase 1α (CK1α) inhibitor. Casein Kinase inhibitor A86 also inhibits of CDK7 (TFIIH) and CDK9 (P-TEFb). Casein Kinase inhibitor A861 induces leukemia cell apoptosis, and has potent anti-leukemic activities. -
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- PROTAC CDK9 degrader-4
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(R)-CDK2 degrader 6
0 Images(R)-CDK2 degrader 6 is the R-enantiomer of CDK2 degrader 6 (HY-176444), a cereblon-based molecular glue degrader of CDK2 with a DC50 of 27 nM. (R)-CDK2 degrader 6 induces ubiquitination and proteasomal degradation of CDK2 by bridging cereblon and CDK2. (R)-CDK2 degrader 6 is applicable for cancer research. -
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Abemaciclib metabolite M20-d8
0 ImagesCat. No.: HY-129336SPurity: 99.26%Synonyms: LSN3106726-d8Abemaciclib metabolite M20-d8 is the deuterium labeled Abemaciclib metabolite M20. Abemaciclib metabolite M20 (LSN3106726), the active metabolite of Abemaciclib, is a selective CDK4/6 inhibitor. -
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NVP-LCQ195
0 ImagesSynonyms: LCQ-195; AT9311NVP-LCQ195 (LCQ-195) is an inhibitor of CDK1/2/3/5/9. NVP-LCQ195 induces cell cycle arrest and eventual apoptotic cell death of multiple myeloma (MM) cells. NVP-LCQ195 triggers decreased amplitude of transcriptional signatures related to oncogenesis, drug resistance and stem cell renewal in MM cell lines. -
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- NU2058
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SGK1-IN-3 hydrochloride
0 ImagesCat. No.: HY-142686APurity: 98.99%SGK1-IN-3 hydrochloride (Compound 3a) is an ATP-competitive SGK1 inhibitor with an IC50 of <1 nM against hSGK1. SGK1-IN-3 hydrochloride blocks the activity of CDK family members. SGK1-IN-3 hydrochloride serves as a P-glycoprotein substrate. SGK1-IN-3 can be used for the research of osteoarthritis. -
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Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.