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Featured researches published by Yurii L. Slominskii.


Journal of Fluorescence | 2002

Spectroscopic Studies of α,γ-Disubstituted Trimethine Cyanine: New Fluorescent Dye for Nucleic Acids

I. V. Valyukh; Vladyslava B. Kovalska; Yurii L. Slominskii; Sergiy M. Yarmoluk

Spectral properties of 3-methyl-2-3-[3-methyl-1,3-benzothiazolo-2(3H)-ylidene]-1,4-cylopentadien-1-yl-1,3-benzothiazolo-3-ium tosylate (Cyan-Cpentd) in a free state and in the complexes with nucleic acids and synthetic polynucleotides have been investigated by absorption and fluorescence spectroscopy. Significant fluorescence intensity enhancement of dye-nucleic acids complexes is observed. For the first time Cyan-Cpentd is proposed as a new probe for nucleic acid detection. Binding mechanism of Cyan-Cpentd is discussed in view of the NA-ligand interaction models.


Biotechnic & Histochemistry | 2014

Development of a quantitative structure activity relations (QSAR) model to guide the design of fluorescent dyes for detecting amyloid fibrils

Di Inshyn; Vladyslava B. Kovalska; Mykhaylo Yu. Losytskyy; Yurii L. Slominskii; O. I. Tolmachev; Sergiy M. Yarmoluk

Abstract Quantitative structure activity relationship (QSAR) studies were performed on a set of polymethine compounds to develop new fluorescent probes for detecting amyloid fibrils. Two different approaches were evaluated for developing a predictive model: part least squares (PLS) regression and an artificial neural network (ANN). A set of 60 relevant molecular descriptors were selected by performing principal component analysis on more than 1600 calculated molecular descriptors. Through QSAR analysis, two predictive models were developed. The final versions produced an average prediction accuracy of 72.5 and 84.2% for the linear PLS and the non-linear ANN procedures, respectively. A test of the ANN model was performed by using it to predict the activity, i.e., staining or non-staining of amyloid fibrils, using 320 compounds. The five candidates whose greatest activities were selected by the ANN model underwent confirmation of their predicted properties by empirical testing. The results indicated that the ANN model potentially is useful for facilitating prediction of activity of untested compounds as dyes for detecting amyloid fibrils.


Dyes and Pigments | 2015

Molecular design of near infrared polymethine dyes: A review

Julia L. Bricks; Alexei Kachkovskii; Yurii L. Slominskii; Andrii O. Gerasov; Sergei V. Popov


Dyes and Pigments | 2006

Polymethine dyes derived from 2,2-difluoro-3,1,2-(2h)-oxaoxoniaboratines with polymethylene bridge groups in the chromophore

Konstantin Zyabrev; Andrei Ya. Il'chenko; Yurii L. Slominskii; Nikolai N. Romanov; A.I. Tolmachev


European Journal of Organic Chemistry | 2008

Design, Synthesis, and Spectral Luminescent Properties of a Novel Polycarbocyanine Series Based on the 2,2-Difluoro-1,3,2-dioxaborine Nucleus

Konstantin Zyabrev; Andrey Doroshenko; Elena K. Mikitenko; Yurii L. Slominskii; Alexei I. Tolmachev


Analytical Biochemistry | 2015

Trimethine cyanine dyes as fluorescent probes for amyloid fibrils: The effect of N,N′-substituents

Marina V. Kuperman; Svitlana Chernii; Mykhaylo Yu. Losytskyy; Dmytro V. Kryvorotenko; Nadiya O. Derevyanko; Yurii L. Slominskii; Vladyslava B. Kovalska; Sergiy M. Yarmoluk


Dyes and Pigments | 2012

New 2,2-difluoro-1,3,2(2H)oxazaborines and merocyanines derived from them

Konstantin Zyabrev; Marina L. Dekhtyar; Yurii Vlasenko; Alexander N. Chernega; Yurii L. Slominskii; A.I. Tolmachev


Quantum Electronics | 1995

Highly stable polymethine-dye-based polymer switches for passive mode locking in neodymium lasers

V. I. Bezrodnyi; Aleksandr A. Ishchenko; L. V. Karabanova; Yurii L. Slominskii


Journal of Physical Organic Chemistry | 2009

Unsymmetrical dyes derived from 7,8-dihydrobenzo[c,d]furo[2,3-f]indole

Iryna G. Davydenko; Aleksei D. Kachkovsky; Marina L. Dekhtyar; Yurii L. Slominskii; A.I. Tolmachev


Quantum Electronics | 1995

Polymer passive laser switches for stimulated emission in the region of 1.3 μm

V. I. Bezrodnyi; N. A. Derevyanko; Aleksandr A. Ishchenko; Yurii L. Slominskii

Collaboration


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Aleksandr A. Ishchenko

National Academy of Sciences of Ukraine

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Sergiy M. Yarmoluk

National Academy of Sciences of Ukraine

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V. I. Bezrodnyi

National Academy of Sciences of Ukraine

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Vladyslava B. Kovalska

National Academy of Sciences of Ukraine

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A.I. Tolmachev

National Academy of Sciences of Ukraine

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Konstantin Zyabrev

National Academy of Sciences of Ukraine

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N. A. Derevyanko

National Academy of Sciences of Ukraine

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Alexei I. Tolmachev

National Academy of Sciences of Ukraine

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Marina L. Dekhtyar

National Academy of Sciences of Ukraine

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Mykhaylo Yu. Losytskyy

National Academy of Sciences of Ukraine

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