Thiocarbonyl Derivatives of Natural Chlorins: Synthesis Using Lawesson's Reagent and a Study of Their Properties

Molecules. 2023 May 20;28(10):4215. doi: 10.3390/molecules28104215.

Abstract

The development of sulfur-containing pharmaceutical compounds is important in the advancement of medicinal chemistry. Photosensitizers (PS) that acquire new properties upon incorporation of sulfur-containing groups or individual sulfur atoms into their structure are not neglected, either. In this work, a synthesis of sulfur-containing derivatives of natural chlorophyll a using Lawesson's reagent was optimized. Thiocarbonyl chlorins were shown to have a significant bathochromic shift in the absorption and fluorescence bands. The feasibility of functionalizing the thiocarbonyl group at the macrocycle periphery by formation of a Pt(II) metal complex in the chemotherapeutic agent cisplatin was shown. The chemical stability of the resulting conjugate in aqueous solution was studied, and it was found to possess a high cytotoxic activity against sarcoma S37 tumor cells that results from the combined photodynamic and chemotherapeutic effect on these cells.

Keywords: Lawesson’s reagent (LR); cisplatin; combined chemotherapy and PDT; photodynamic therapy (PDT); photosensitizers (PS); platinum complex.

MeSH terms

  • Chlorophyll A
  • Organothiophosphorus Compounds* / chemistry
  • Sulfur

Substances

  • 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide
  • chlorin
  • Chlorophyll A
  • Organothiophosphorus Compounds
  • Sulfur