Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Stepan G. Pilyo"'
Inhibition of Xanthine Oxidase by Pyrazolone Derivatives Bearing a 4-(Furan-2-yl)benzoic Acid Moiety
Autor:
Alona V. Beiko, Oleksandr L. Kobzar, Maryna V. Kachaeva, Stepan G. Pilyo, Vsevolod Yu. Tanchuk, Andriy I. Vovk
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 21, Iss 4, Pp 27-35 (2023)
The pyrazolone-based 4-(furan-2-yl)benzoic acids have been synthesized and studied as xanthine oxidase inhibitors. This enzyme is one of the therapeutic targets for the treatment of hyperuricemia and related diseases. The compounds studied have found
Externí odkaz:
https://doaj.org/article/c837628d2ff64610be2c10ef61c2a44b
Autor:
Nataliya Obernikhina, Yevheniia Velihina, Maryna V. Kachaeva, Stepan G. Pilyo, Oleksiy Kachkovsky
Publikováno v:
Ukr. Bioorg. Acta 2021, Vol. 16, N1. 16:34-43
The binding affinity of model peptide moieties (Pept) and heterocyclic bases involving 1,3-oxazoles that are condensed with pyridine and pyrimidine as pharmacophores (Pharm) was investigated in silico and analyzed within the «fragment-to-fragment»
Autor:
Vlasyslav Buldenko, Oleksandr L. Kobzar, Yuriy Shulha, Andriy I. Vovk, Diana Hodyna, Stepan G. Pilyo, Volodymyr Brovarets, V. O. Sinenko
Publikováno v:
Ukr. Bioorg. Acta 2020, Vol. 15, N2. 15:33-40
Thiazole-containing derivatives of rhodanine-3-alkanoic acids with propanoic or undecanoic acid groups were synthesized and evaluated as inhibitors of some protein tyrosine phosphatases and glutathione S-transferases. The rhodanines bearing longer ca
Autor:
Nataliya Obernikhina, Stepan G. Pilyo, Volodymyr Brovarets, Oleksiy Kachkovsky, Yevheniia Velihina, Maryna V. Kachaeva
Publikováno v:
Ukr. Bioorg. Acta 2020, Vol. 15, N2. 15:49-59
The binding affinity of model aromatic amino acids and heterocycles and their derivatives condensed with pyridine were investigated in silico and are presented in the framework of fragment-to-fragment approach. The presented model describes interacti
Autor:
Stepan G. Pilyo, Victor V. Zhirnov, V. S. Brovarets, Emma A. Harden, Mark N. Prichard, Nataliya V. Velychko, Mykhailo Y. Brusnakov, Scott H. James, Oleksandr V. Golovchenko, E. R. Abdurakhmanova
Publikováno v:
Medicinal Chemistry Research. 29:1669-1675
A series of derivatives of 5-hydroxyalkylamino-1,3-oxazoles were synthesized. Among these derivatives, 5 compounds have been evaluated for their activities against a normal laboratory human cytomegalovirus (HCMV) strain, AD169, in human foreskin fibr
Autor:
Andriy V. Kozytskiy, Maryna V. Kachaeva, O. V. Shablykina, R. N. Vydzhak, Volodymyr Brovarets, Stepan G. Pilyo, V. S. Moskvina
Publikováno v:
Ukr. Bioorg. Acta 2020, Vol. 15, N1. 15:26-33
A versatile and efficient three-component cyclization of methyl 4-(o-hydroxyphenyl)-2,4-dioxobutanoates 1, N-substituted isatins 2, and primary amines 3 was explored to synthesize of 2H-spiro[chromeno[2,3-c]pyrrole-1,3'-indoline]-2',3,9-triones. We o
Autor:
V.V. Sukhoveev, A.V. Tatarchuk, M.V. Kachaeva, Stepan G. Pilyo, O.V. Sukhoveev, A. I. Vovk, Oleksandr L. Kobzar, Volodymyr Brovarets
Publikováno v:
Reports of the National Academy of Sciences of Ukraine. :74-82
Autor:
Oleksiy Kachkovsky, Maryna V. Kachaeva, Yulia S. Kovalenko, V. M. Prokopenko, Stepan G. Pilyo, Volodymyr Brovarets, Nataliya Obernikhina, Diana Hodyna
Publikováno v:
Journal of Heterocyclic Chemistry. 56:3122-3134
Autor:
Emma A. Harden, Volodymyr Brovarets, Caroll B. Hartline, Victor V. Zhirnov, Maryna V. Kachaeva, Stepan G. Pilyo, Mark N. Prichard
Publikováno v:
Medicinal Chemistry Research. 28:1205-1211
Ten 5-functionalized derivatives of 1,3-oxazole-4-carboxylate and 1,3-oxazole-4-carbonitrile were synthesized and their antiviral activities against the human cytomegalovirus (HCMV) were evaluated in vitro. Bioassays showed that seven compounds exhib
Autor:
Volodymyr Brovarets, Andriy V. Kozytskiy, Stepan G. Pilyo, R. N. Vydzhak, O. V. Shablykina, V. S. Moskvina, Svitlana Ya. Panchishin, Maryna V. Kachaeva
Publikováno v:
Molecular Diversity
Graphic abstract An efficient and practical synthetic procedure for libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones using a multicomponent process is presented. A convenient synthetic procedure for obtaining functionalized 3-(2-