Discovery and Structure–Activity Relationships of Novel Template, Truncated 1′-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators

Lignende værker

• Polypharmacology of N(6)-(3-Iodobenzyl)adenosine-5′-N-methyluronamide (IB-MECA) and Related A(3) Adenosine Receptor Ligands: Peroxisome Proliferator Activated Receptor (PPAR) γ Partial Agonist and PPARδ Antagonist Activity Suggests Their Antidiabetic Potential
  af: Yu, Jinha, et al.
  Udgivet: (2017)
• Design and Synthesis of 2,6-Disubstituted-4′-Selenoadenosine-5′-N,N-Dimethyluronamide Derivatives as Human A(3) Adenosine Receptor Antagonists
  af: Choi, Hongseok, et al.
  Udgivet: (2021)
• Diallyl Biphenyl-Type Neolignans Have a Pharmacophore of PPARα/γ Dual Modulators
  af: Han, Yujia, et al.
  Udgivet: (2020)
• LJ-1888, a selective antagonist for the A3 adenosine receptor, ameliorates the development of atherosclerosis and hypercholesterolemia in apolipoprotein E knock-out mice
  af: Park, Jong-Gil, et al.
  Udgivet: (2018)
• Structure-Activity Relationships of Acyclic Selenopurine Nucleosides as Antiviral Agents
  af: Sahu, Pramod K., et al.
  Udgivet: (2017)