Isolation, reactivity, pharmacological activities and total synthesis of hispanolone and structurally related diterpenes from Labiatae plants

Bioorg Med Chem Lett. 2020 Nov 1;30(21):127498. doi: 10.1016/j.bmcl.2020.127498. Epub 2020 Aug 17.

Abstract

Hispanolone is a furolabdane diterpene isolated from Ballota hispanica, whose natural product chemistry has been summarized and updated here, including several aspects associated with the isolation, structure determination, hemisynthesis, total synthesis, and pharmacology, and related hispanolone diterpenoids that have attracted the interest of different laboratories from diverse perspective and expertise in the last forty-two years.

Keywords: Ballota genus; Diterpenes; Hemisynthesis; Hispanolone; Isolation; Labiatae family; Natural products; Pharmacology; Reactivity; Total synthesis.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / isolation & purification
  • Anti-Bacterial Agents / pharmacology*
  • Antineoplastic Agents, Phytogenic / chemistry
  • Antineoplastic Agents, Phytogenic / isolation & purification
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Ballota / chemistry*
  • Biological Products / chemistry
  • Biological Products / isolation & purification
  • Biological Products / pharmacology*
  • Diterpenes / chemistry
  • Diterpenes / isolation & purification
  • Diterpenes / pharmacology*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / isolation & purification
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Molecular Conformation

Substances

  • Anti-Bacterial Agents
  • Antineoplastic Agents, Phytogenic
  • Biological Products
  • Diterpenes
  • Enzyme Inhibitors
  • hispanolone