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
(488)
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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
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19-epi-Scholaricine
0 Images19-epi-Scholaricine is an orally active indole alkaloid. 19-epi-Scholaricine downregulates the expression of profibrotic/apoptotic proteins (HRAS, HSP90AA1, KDR) and upregulates the expression of cell cycle-related protein (CDK2). 19-epi-Scholaricine suppresses ROS production and reduces the release of inflammatory mediators, thereby attenuating podocyte apoptosis, renal inflammation and oxidative stress by inhibiting AKT/mTOR. 19-epi-Scholaricine can be used in the research of chronic glomerulonephritis and membranous nephropathy. -
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Cdk15 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS26883Cdk15 Rat Pre-designed siRNA Set A contains three designed siRNAs for Cdk15 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
Components
Cdk15 siRNA-1: 5 nmol (HPLC)
Cdk15 siRNA-2: 5 nmol (HPLC)
Cdk15 siRNA-3: 5 nmol (HPLC)
siRNA Negative Control: 5 nmol (HPLC)
FAM-labeled siRNA Negative Control: 5 nmol (HPLC)
GAPDH siRNA Positive Control: 5 nmol (HPLC)
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Aminopurvalanol A (Standard)
0 ImagesCat. No.: HY-104013RCAS No.: 220792-57-4Aminopurvalanol A (Standard) is the analytical standard of Aminopurvalanol A (HY-104013). This product is intended for research and analytical applications. Aminopurvalanol A is a potent, selective, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of physiological capacitation-dependent actin polymerization. -
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CDK8-IN-4 (Standard)
0 ImagesCat. No.: HY-111465RCAS No.: 1613638-82-6 -
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MeBIO (Standard)
0 ImagesCat. No.: HY-103221RCAS No.: 667463-95-8 -
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PROTAC CDK9 Degrader-1 (Standard)
0 ImagesCat. No.: HY-103628RCAS No.: 2118356-96-8 -
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CCT68127
0 ImagesCat. No.: HY-123826CAS No.: 660822-23-1Synonyms: αSβR-21CCT68127 is an orally active CDK inhibitor. CCT68127 can be used in anti-cancer research. -
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Amantadine hydrochloride (Standard)
0 ImagesSynonyms: 1-Adamantanamine hydrochloride (Standard); 1-Adamantylamine hydrochloride (Standard); 1-Aminoadamantane hydrochloride (Standard)Amantadine (hydrochloride) (Standard) is the analytical standard of Amantadine (hydrochloride). This product is intended for research and analytical applications. Amantadine (1-Adamantanamine) hydrochloride is an orally avtive and potent antiviral agent with activity against influenza A viruses. Amantadine hydrochloride inhibits several ion channels such as NMDA and M2, and also inhibits Coronavirus ion channels. Amantadine hydrochloride also has anti-orthopoxvirus and anticancer activity. Amantadine hydrochloride can be used for Parkinson's disease, postoperative cognitive dysfunction (POCD) and COVID-19 research. -
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Dinaciclib (Standard)
0 ImagesCat. No.: HY-10492RCAS No.: 779353-01-4Synonyms: SCH 727965 (Standard)Dinaciclib (Standard) is the analytical standard of Dinaciclib (HY-10492). This product is intended for research and analytical applications. Dinaciclib (SCH 727965) is a potent inhibitor of CDK, with IC50s of 1 nM, 1 nM, 3 nM, and 4 nM for CDK2, CDK5, CDK1, and CDK9, respectively. -
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Momilactone B
0 ImagesMomilactone B is an inhibitor of α-amylase and α-glucosidase, with an IC50 of 146.85 μg/mL against Aspergillus oryzae α-amylase and an IC50 of 612.03 μg/mL against Saccharomyces cerevisiae α-glucosidase. Momilactone B upregulates the expression of p21Waf1/Cip1, reduces the kinase activity of Cdk4 and Cdk6, induces cell cycle arrest and apoptosis in cancer cells, and triggers irreversible cell death via cell membrane damage. Momilactone B inhibits the growth of neighboring plant species and serves as a major contributing factor to the allelopathy of rice. Momilactone B can be used in studies related to rice allelopathy, type 2 diabetes, colon cancer and leukemia. -
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Antitrypanosomal agent 31
0 ImagesCat. No.: HY-183529CAS No.: 551919-54-1Antitrypanosomal agent 31 is an antitrypanosoma agent with a pEC50 of 6.4. Antitrypanosomal agent 31 inhibits GSK-3β, CDK-2, and CDK-4 with pIC50s of 5.8, 6.9, and 7.1, respectively. Antitrypanosomal agent 31 can be used for the research of human african trypanosomiasis. -
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CGP60474 (Standard)
0 ImagesCat. No.: HY-11009RCAS No.: 164658-13-3CGP60474 (Standard) is the analytical standard of CGP60474 (HY-11009). This product is intended for research and analytical applications. CGP60474, a highly potent anti-endotoxemic agent, is a potent cyclin-dependent Kinase (CDK) inhibitor (IC50 values are 26, 3, 4, 216, 10, 200 and 13 nM for CDK1/B, CDK2/E, CDK2/A, CDK4/D, CDK5/p25, CDK7/H and CDK9/T, respectively). CGP60474 is a selective and ATP-competitive PKC inhibitor. -
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GSK3326595 (Standard)
0 ImagesSynonyms: EPZ015938 (Standard)GSK3326595 (Standard) is the analytical standard of GSK3326595 (HY-101563). This product is intended for research and analytical applications. GSK3326595 is a protein arginine methyltransferase 5 (PRMT5) inhibitor. GSK3326595 decreases SARS-CoV-2 infection, inhibits cancer cell proliferation and induces pro-inflammatory macrophage polarization and increases hepatic triglyceride levels without affecting atherosclerosis. GSK3326595 can be used for research of relapsed/refractory mantle cell lymphoma. -
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(-)-Enitociclib (Standard)
0 ImagesCat. No.: HY-103019BRCAS No.: 1610408-96-2Synonyms: (R)-Enitociclib (Standard); (-)-BAY-1251152 (Standard); (-)-VIP152 (Standard)(-)-Enitociclib (Standard) is the analytical standard of (-)-Enitociclib (HY-103019B). This product is intended for research and analytical applications. (-)-Enitociclib ((R)-Enitociclib) is an enantiomer of Enitociclib (HY-103019E) with an optical rotation of (-). Enitociclib is a selective CDK9 inhibitor and apoptosis inducer. Enitociclib inhibits CDK9 activity and reduces the phosphorylation of Ser2 in the carboxyl-terminal domain (CTD) of RNA polymerase Pol II, thereby downregulating the transcription of key oncogenes such as MYC and MCL1. Enitociclib has anti-proliferative activity targeting MYC+ lymphoma and multiple myeloma (MM) cells, and has synergistic effects with Bortezomib (HY-10227) and Lenalidomide (HY-A0003), and can be used in the research of hematological malignancies. -
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5-Iodo-indirubin-3'-monoxime (Standard)
0 ImagesCat. No.: HY-111930RCAS No.: 331467-03-95-Iodo-indirubin-3'-monoxime (Standard) is the analytical standard of 5-Iodo-indirubin-3'-monoxime (HY-111930). This product is intended for research and analytical applications. 5-Iodo-indirubin-3'-monoxime is a potent GSK-3β, CDK5/P25 and CDK1/cyclin B inhibitor, competing with ATP for binding to the catalytic site of the Kinase, with IC50s of 9, 20 and 25 nM, respectively. -
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BSJ-03-123 (Standard)
0 ImagesCat. No.: HY-111556RCAS No.: 2361493-16-3BSJ-03-123 (Standard) is the analytical standard of BSJ-03-123 (HY-111556). This product is intended for research and analytical applications. BSJ-03-123 is a PROTAC connected by ligands for Cereblon and CDK as a potent and novel CDK6-selective small-molecule degrader. -
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CDK modulator 1
0 ImagesCat. No.: HY-W809647CAS No.: 1203565-13-2 -
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OM137
0 ImagesCat. No.: HY-123279CAS No.: 292170-13-9OM137 is an aurora kinase inhibitor, with an IC50 of 21.7 μM (Aurora A kinase) and 2.4 μM (Aurora B kinase). OM137 also inhibits Cdk1/cyclinB and Cdk5/p25 with an approximate IC50 of 20 μM. OM137 reduces spindle checkpoint-signaling proteins (Mad2 and BubR1) at the kinetochores of chromosomes. -
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CDK9-IN-8 (Standard)
0 ImagesCat. No.: HY-102039RCAS No.: 2105956-51-0CDK9-IN-8 (Standard) is the analytical standard of CDK9-IN-8 (HY-102039). This product is intended for research and analytical applications. CDK9-IN-8 is a highly effective and selective CDK9 inhibitor with an IC50 of 12 nM. -
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CDK8-IN-16
0 ImagesCat. No.: HY-171174CAS No.: 1860885-61-5CDK8-IN-16 (Compound 51) is an orally active dual inhibitor for CDK8 and CDK19 wih IC50 of 5.1 nM and 5.6 nM. CDK8-IN-16 inhibits the phospho-STAT1SER727 with an IC50 of 17.9 nM in SW620 cell, inhibits WNT signaling pathway with an IC50 of 7.2 nM in 7dF3 cell. CDK8-IN-16 exhibits good pharmacokinetic characteristics in rat models with an oral bioavailability of 57%. -
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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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