Evaluation of indole esters as inhibitors of p60(c-Src) receptor tyrosine kinase and investigation of the inhibition using receptor docking studies

J Enzyme Inhib Med Chem. 2003 Dec;18(6):485-90. doi: 10.1080/14756360310001612211.

Abstract

Several indole esters were tested as inhibitors of tyrosine kinase p60(c-Src). Compound (4) was found fairly active against the enzyme with IC50 = 1.34 microM. DOCK methodology was used to asses our inhibitors for their inhibitory potency against tyrosine kinase. The docking results showed that compounds (4), (25) and (26) were bound to the active site of the enzyme Lys 295 of p60(c-Src) tyrosine kinase. Both activity and docking studies showed a parallel result, with compound (4) having a better interaction with the enzyme active site and also greater activity than the other compounds, indicating a potential role as new lead inhibitor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Chickens
  • Enzyme Inhibitors / metabolism
  • Enzyme Inhibitors / pharmacology*
  • Esters
  • Indoles / metabolism
  • Indoles / pharmacology*
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Structure, Secondary
  • Proto-Oncogene Proteins pp60(c-src) / antagonists & inhibitors*
  • Proto-Oncogene Proteins pp60(c-src) / metabolism
  • Software
  • Structure-Activity Relationship
  • Substrate Specificity

Substances

  • Enzyme Inhibitors
  • Esters
  • Indoles
  • Proto-Oncogene Proteins pp60(c-src)