1174062-36-2Relevant academic research and scientific papers
New insight into nucleo α-amino acids – Synthesis and SAR studies on cytotoxic activity of β-pyrimidine alanines
Bretner, Maria,Ignatowska, Jolanta,Karatsai, Olena,Mironiuk-Puchalska, Ewa,Wielechowska, Monika,Grze?kowiak, Piotr,Jolanta R?dowicz, Maria,Koszytkowska-Stawińska, Mariola,Wińska, Patrycja
, (2020)
Three series of the β-pyrimidine alanines, including willardiine - a naturally occurring amino acid, were prepared from the L-serine-derived sulfamidates. Compounds 3b, 4a and 4b demonstrated antiproliferative activity toward the studied cancer cell lines, albeit the effect of these compounds on human brain astrocytoma MOG-G-CCM cells was more significant than on human neuroblastoma SK-N-AS cells. The cytosine analog of willardiine, compound 4b, reduced viability of MOG-G-CCM cells with EC50 = 36 ± 2 μM, more effectively than AMPA antagonist GYKI 52466. Willardiine showed possible capability of affecting invasiveness of glioblastoma U251 MG cells with no effect on their viability and morphology. Compound 3d, the ethyl ester of willardiine, featured activity toward binding domain hHS1S2I of the GluR2 receptor. Docking analysis revealed that the location mode of compound 3d at the S1S2 domain of hGluR2 (PDB ID: 3R7X) might differ from that of willardiine.
Conformationally controlled, thymine-based α-nucleopeptides
Geotti-Bianchini, Piero,Crisma, Marco,Peggion, Cristina,Bianco, Alberto,Formaggio, Fernando
supporting information; experimental part, p. 3178 - 3180 (2009/12/01)
Rigid peptide backbones and backbone-to-side chain H-bonds permit the design of α-nucleopeptides with known 3D-structure; thymine-thymine base pairing is also observed.
