Hit to Leads with Cytotoxic Effect in Leukemic Cells: Total Synthesis Intermediates as a Molecule Treasure Chest.
Hans-René BjørsvikBjorn Tore GjertsenVijayaragavan ElumalaiPublished in: ChemMedChem (2020)
A previously designed and developed 12-step total synthesis that includes [1,1'-biphenyl]-2-amine and carbazole intermediates and that ultimately produces the carbazole alkaloid carbazomycin G was exploited as a screening compound library with the goal of identifying potential lead compound(s) with cytotoxic effect. These compounds were investigated by using in-vitro tests involving the two human cell lines HL-60 and MOLM-13, which both model acute myeloid leukaemia (AML). The in-vitro biological test results were used together with the molecular structures of the various intermediates in a concise SAR analysis. Several of the intermediates revealed cytotoxicity (IC50 <10-4 M), although the final natural product carbazomycin G did not reveal cytotoxicity versus the two said human cell lines.
Keyphrases
- endothelial cells
- acute myeloid leukemia
- induced pluripotent stem cells
- pluripotent stem cells
- single cell
- liver failure
- high resolution
- dendritic cells
- bone marrow
- dna methylation
- intensive care unit
- gene expression
- cell death
- genome wide
- oxidative stress
- signaling pathway
- acute lymphoblastic leukemia
- mass spectrometry
- climate change
- allogeneic hematopoietic stem cell transplantation
- hepatitis b virus
- mechanical ventilation