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Analogs of penfluridol as chemotherapeutic agents with reduced central nervous system activity
Authors:Md Ashraf-Uz-Zaman  Md Sanaullah Sajib  Luca Cucullo  Constantinos M. Mikelis  Nadezhda A. German
Affiliation:Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, School of Pharmacy, Amarillo, TX 79106, United States
Abstract:Several recent reports have highlighted the feasibility of the use of penfluridol, a well-known antipsychotic agent, as a chemotherapeutic agent. In vivo experiments have confirmed the cytotoxic activity of penfluridol in triple-negative breast cancer model, lung cancer model, and further studies have been proposed to assess its anticancer activity and viability for the treatment of glioblastomas. However, penfluridol anticancer activity was observed at a dosage significantly higher than that administered in antipsychotic therapy, thus raising the concern for the potential onset of CNS side effects in patients undergoing intensive pharmacological treatment. In this study, we evaluate the potential CNS toxicity of penfluridol side by side with a set of analogs.
Keywords:ALP  alkaline phosphatase creatine kinase  ALT  alanine aminotransferase  AST  aspartate aminotransferase  BBB  blood brain barrier  BOC  BUN  blood urea nitrogen test  CK  creatine kinase  CNS  central nervous system  D1-5  dopamine receptor subtypes  DAT  dopamine transporter  DCM  dichloromethane  DOR  delta opioid receptor  DPPH  1,1′-bis(diphenylphosphino)ferrocene  ESI  electrospray ionization  EtOH  ethanol  FDA  Food and Drug Administration  GI  gastrointestinal  GLDH  glutamine dehydrogenase  H1-2  histamine receptor subtypes  5HT  serotonin receptors  half-maximum inhibitory concentration  i.p  intraperitoneal injection  Ki  inhibition constant  KOR  kappa opioid receptor  LC  liquid chromatography  LC-MS  liquid chromatography-mass spectrometry  LLC luc  mouse-derived luciferin expressing Lewis lung carcinoma cell line  MDA MB231  human triple-negative breast cancer cell line  MOR  mu opioid receptor  MTT  3-[4,5-dimethylthiazol-2-yl]-2,5-dimethyltetrazolium bromide  NET  norepinephrine transporter  NMR  nuclear magnetic resonance  r.t  room temperature  SERT  serotonin transporter  THF  tetrahydrofuran  TLC  thin-layer chromatography  Penfluridol  Anticancer agent  Central nervous system  Repurposing  Toxicity  Optimization
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