European Journal of Medicinal Chemistry Reports (Dec 2022)

An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans

  • Niels V. Heise,
  • Sophie Hoenke,
  • Immo Serbian,
  • René Csuk

DOI
https://doi.org/10.1016/j.ejmcr.2022.100073
Journal volume & issue
Vol. 6
p. 100073

Abstract

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Ursolic acid was used as a convenient starting material for a three-step partial synthesis of corosolic acid. Corosolic acid was acetylated, and an amide linker was attached followed by a rhodamine B unit at the distal end of the linker. Especially compounds holding a piperazinyl or homopiperazinyl linker held exceptional cytotoxicity for several human tumor cell lines. For example, homopiperazinyl spacered 11 showed EC50 ​= ​2 ​nM for A2780 ​cells combined with high tumor cell/non-tumor cell selectivity (compound 11: EC50 ​= ​0.122 ​μM for non-malignant NIH 3T3). Thus, compound 11 currently represents one of the most cytotoxic triterpene derivatives holding both superior cytotoxicity combined with high selectivity (SI A2780 vs NIH 3T3 ​> ​60). Staining experiments showed this compound to act as a mitocan. This makes 11 an interesting compound for further studies or as a lead substance.

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