1. Signaling Pathways
  2. Cell Cycle/DNA Damage
  3. CDK
  4. CDK17 Isoform

CDK17

CDK17 (cyclin-dependent kinase 17), also known as PCTAIRE2, belongs to the PCTAIRE subfamily of cyclin-dependent serine/threonine kinases and is predominantly expressed in terminally differentiated neurons, supporting a specialized role distinct from canonical cell-cycle CDKs[1]. Mechanistically, CDK17 participates in neuronal signaling networks and has been associated with protein interaction complexes linked to neuronal differentiation and intracellular regulatory processes[1][2]. In disease-related models, increased PCTAIRE2 expression has been reported in amyloid precursor protein (APP)-dependent experimental systems and has been associated with Alzheimer-related molecular pathology, suggesting relevance to neurodegenerative signaling pathways rather than classical proliferative cell-cycle control[3]. Compared with related PCTAIRE family members, including CDK16 and CDK18, CDK17 remains substantially less characterized, and current evidence highlights its neuronal enrichment as a distinguishing biological feature[4]. For experimental research applications, CDK17 is primarily investigated through expression profiling, protein-interaction studies, and neurodegeneration-associated cellular models, whereas selective CDK17-targeted pharmacological inhibitors have not been well established in the published literature cited here[1][3][4].

CDK17 Related Products (2):

Cat. No. Product Name Effect Purity
  • HY-14660
    Dabrafenib
    Degrader 99.94%
    Dabrafenib (GSK2118436A) is an ATP-competitive inhibitor of Raf with IC50s of 5 nM and 0.6 nM for C-Raf and B-RafV600E, respectively.
  • HY-137346
    DD-03-156
    99.90%
    DD-03-156 is a potent and selective degrader of CDK17 and LIMK2. DD-03-156 is exquisite and makes an advanced starting point for the development of a chemical probe for the degradation of CDK17.