N1-Benzyl Tryptamine Pan-SHIP1/2 Inhibitors: Synthesis and Preliminary Biological Evaluation as Anti-Tumor Agents

Molecules. 2022 Dec 2;27(23):8451. doi: 10.3390/molecules27238451.

Abstract

Inhibition of phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase (SHIP) with small molecule inhibitors leads to apoptosis in tumor cells. Inhibitors that target both SHIP1 and SHIP2 (pan-SHIP1/2 inhibitors) may have benefits in these areas since paralog compensation is not possible when both SHIP paralogs are being inhibited. A series of tryptamine-based pan-SHIP1/2 inhibitors have been synthesized and evaluated for their ability to inhibit the SHIP paralogs. The most active compounds were also evaluated for their effects on cancer cell lines.

Keywords: SHIP1; SHIP2; antitumor; medicinal chemistry; phosphatase; tryptamine.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Cell Line
  • Humans
  • Neoplasms* / drug therapy
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases / metabolism
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphorylation

Substances

  • Phosphoric Monoester Hydrolases
  • Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
  • Antineoplastic Agents