The design, synthesis and physical chemical properties of novel human vasopressin V2-receptor antagonists optimized for parenteral delivery

Bioorg Med Chem Lett. 2000 Apr 17;10(8):783-6. doi: 10.1016/s0960-894x(00)00095-0.

Abstract

Ionizable groups were introduced onto the 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine scaffold of the vasopressin V2-antagonist WAY-VPA-985 in the search for molecules optimized for parenteral formulation. The synthesis and structure activity relationships (SAR) are presented together with solubility data in a model parenteral system. The amine, WAY-140288 (4f), was chosen for further development. p6

MeSH terms

  • Antidiuretic Hormone Receptor Antagonists*
  • Benzamides / chemical synthesis
  • Benzamides / chemistry*
  • Benzodiazepines / chemistry*
  • Humans
  • Infusions, Parenteral
  • Pyrroles / chemical synthesis
  • Pyrroles / chemistry*
  • Structure-Activity Relationship

Substances

  • Antidiuretic Hormone Receptor Antagonists
  • Benzamides
  • Pyrroles
  • Benzodiazepines
  • lixivaptan