3-Pyridylisoxazoles as prototypes of antiaggregatory agents
- Autores: Demina O.V.1, Belikov N.E.1, Varfolomeev S.D.1, Khodonov A.A.1
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Afiliações:
- N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
- Edição: Volume 67, Nº 5 (2018)
- Páginas: 866-877
- Seção: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/242528
- DOI: https://doi.org/10.1007/s11172-018-2151-2
- ID: 242528
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Resumo
A series of 5-alkyl-3-pyridylisoxazoles was synthesized using the 3-(3-pyridyl)isoxazole scaff old. All compounds of the series possessed antiaggregatory activity in the concentration range of 6•10–6–6•10–4 mol L–1. Analysis of the experimental data on the antiaggregatory activity revealed the presence of spatial constraints for the alkyl substituents in position 5 of the isoxazole ring. 5-Alkyl-3-(3-pyridyl)isoxazoles are rather selective for platelet membrane receptors.
Sobre autores
O. Demina
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Autor responsável pela correspondência
Email: ovd@sky.chph.ras.ru
Rússia, 4 ul. Kosigina, Moscow, 119334
N. Belikov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Rússia, 4 ul. Kosigina, Moscow, 119334
S. Varfolomeev
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Rússia, 4 ul. Kosigina, Moscow, 119334
A. Khodonov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Rússia, 4 ul. Kosigina, Moscow, 119334
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