Bombesin receptor antagonists. 5 new irreversible alkylating analogues

Farmaco. 1992 Jun;47(6):855-67.

Abstract

New alkylating bombesin analogues were synthesized in order to increase their solubility and stability in aqueous solutions. The best compromise between these parameters and the biological properties (receptor binding and antagonistic activity) was achieved with 4-[bis(2-chloro-ethylamino)]benzoyl derivatives of the BN (7-14) octapeptide carrying a (13-14) reduced peptide bond independently of the presence of a His12 residue, either free or protected.

MeSH terms

  • Alkylating Agents / chemistry
  • Alkylating Agents / pharmacology*
  • Amino Acid Sequence
  • Chemical Phenomena
  • Chemistry, Physical
  • Iodine Radioisotopes
  • Mitogens
  • Molecular Sequence Data
  • Receptors, Bombesin
  • Receptors, Neurotransmitter / antagonists & inhibitors*
  • Solubility

Substances

  • Alkylating Agents
  • Iodine Radioisotopes
  • Mitogens
  • Receptors, Bombesin
  • Receptors, Neurotransmitter