1. Academic Validation
  2. Towards identifying potent new hits for glioblastoma

Towards identifying potent new hits for glioblastoma

  • Medchemcomm. 2018 Oct 2;9(11):1850-1861. doi: 10.1039/c8md00436f.
Chris Sherer 1 Saurabh Prabhu 2 David Adams 1 Joseph Hayes 3 Farzana Rowther 4 Ibrahim Tolaymat 5 Tracy Warr 4 Timothy J Snape 1
Affiliations

Affiliations

  • 1 School of Pharmacy and Biomedical Sciences , University of Central Lancashire , Preston , Lancashire PR1 2HE , UK . Email: tjsnape@uclan.ac.uk.
  • 2 School of Pharmacy , University of East Anglia , Norwich Research Park , Norwich NR4 7TJ , UK.
  • 3 School of Physical Sciences and Computing , University of Central Lancashire , Preston , Lancashire PR1 2HE , UK.
  • 4 Brain Tumour Research Centre , University of Wolverhampton , Wulfruna Street , Wolverhampton , WV1 1LY , UK.
  • 5 Faculty of Medical Science , Anglia Ruskin University , Bishop Hall Lane , Chelmsford , Essex CM1 1SQ , UK.
Abstract

Glioblastoma is a devastating disease of the brain and is the most common malignant primary brain tumour in adults. The prognosis for patients is very poor with median time of survival after diagnosis measured in months, due in part to the tumours being highly aggressive and often resistant to chemotherapies. Alongside the ongoing research to identify key factors involved in tumour progression in glioblastoma, medicinal chemistry approaches must also be used in order to rapidly establish new and better treatments for brain tumour patients. Using a computational similarity search of the ZINC database, alongside traditional analogue design by medicinal chemistry intuition to improve the breadth of chemical space under consideration, six new hit compounds (14, 16, 18, 19, 20 and 22) were identified possessing low micromolar activity against both established cell lines (U87MG and U251MG) and patient-derived cell cultures (IN1472, IN1528 and IN1760). Each of these scaffolds provides a new platform for future development of a new therapy in this area, with particular promise shown against glioblastoma subtypes that are resistant to conventional chemotherapeutic agents.

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