نتایج جستجو برای: hoechst 33258

تعداد نتایج: 2303  

Journal: :Nucleic acids research 2001
C E Bostock-Smith S A Harris C A Laughton M A Searle

NMR analysis and molecular dynamics simulations of d(GGTAATTACC)(2) and its complex with a tetrahydropyrimidinium analogue of Hoechst 33258 suggest that DNA minor groove recognition in solution involves a combination of conformational selection and induced fit, rather than binding to a preorganised site. Analysis of structural fluctuations in the bound and unbound states suggests that the degre...

Journal: :Journal of The Serbian Chemical Society 2023

In the present study, a zinc(II) complex with 4-ethynyl-2,2?-bipyridine (ebpy), [Zn(ebpy)Cl2], was synthesized and characterized by spectroscopic (1H NMR, IR UV-Vis) methods molar conductivity measurement. The crystal structure of [Zn(ebpy)Cl2] determined single-crystal X-ray diffraction analysis, confirming bidentate coordination ebpy ligand through its two nitrogen atoms, while remaining site...

Journal: :Bioscience, biotechnology, and biochemistry 2002
Eriko Michishita Naoto Matsumura Toshihiro Kurahashi Toshikazu Suzuki Hideki Ogino Michihiko Fujii Dai Ayusawa

We tested various thymidine analogues for induction of a senescence-like phenomenon in HeLa cells. CldU, BrdU, and IdU similarly induced the morphology of senescent cells and typical senescence markers. Thymidine analogues other than 5-halogenated forms caused only cell death. BrdU efficiently killed the cells in cooperation with irradiation with light and a brief treatment with Hoechst 33258, ...

Journal: :Nucleic acids research 2000
E Gavathiotis G J Sharman M S Searle

The solution structure of the dodecamer duplex d(CTTTTGCAAAAG)(2)and its 2:1 complex with the bis -benzimidazole Hoechst 33258 has been investigated by NMR and NOE-restrained molecular dynamics (rMD) simulations. Drug molecules are bound in each of the two A-tracts with the bulky N-methylpiperazine ring of each drug located close to the central TG (CA) step, binding essentially to the narrow mi...

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