4.6 Article

Solution and Solid-State Analysis of Binding of 13-Substituted Berberine Analogues to Human Telomeric G-quadruplexes

期刊

CHEMISTRY-AN ASIAN JOURNAL
卷 11, 期 7, 页码 1107-1115

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201600116

关键词

alkaloids; berberine; crystal structure; G-quadruplexes; telomeric DNA; X-ray diffraction

资金

  1. Ente Cassa di Risparmio di Firenze, Italy [2014.0309]
  2. Italian Ministry of Economic Development within the sixth call of the EuroTransBio initiative, Project BER.T.A [01705]
  3. SENESCYT (Quito, Ecuador)
  4. Universidad Tecnica Particular de Loja (Loja, Ecuador)

向作者/读者索取更多资源

The interaction between 13-phenylalkyl and 13-diphenylalkyl berberine derivatives (NAX) and human telomeric DNA G4 structures has been investigated by both spectroscopic and crystallographic methods. NAX042 and NAX053 are the best compounds improving the performance of the natural precursor berberine. This finding is in agreement with the X-ray diffraction result for the NAX053-Tel12 adduct, showing the ligand which interacts via -stacking, sandwiched at the interface of two symmetry-related quadruplex units, with its benzhydryl group contributing to the overall stability of the adduct by means of additional -stacking interactions with the DNA residues. The berberine derivatives were also investigated for their cytotoxic activity towards a panel of human cancer cell lines. Compounds NAX042 and NAX053 affect the viability of cancer cell lines in a dose-dependent manner.

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