3-Pyridylisoxazoles as prototypes of antiaggregatory agents
- Авторлар: Demina O.V.1, Belikov N.E.1, Varfolomeev S.D.1, Khodonov A.A.1
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Мекемелер:
- N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
- Шығарылым: Том 67, № 5 (2018)
- Беттер: 866-877
- Бөлім: Full Articles
- URL: https://journals.rcsi.science/1066-5285/article/view/242528
- DOI: https://doi.org/10.1007/s11172-018-2151-2
- ID: 242528
Дәйексөз келтіру
Аннотация
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.
Авторлар туралы
O. Demina
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: ovd@sky.chph.ras.ru
Ресей, 4 ul. Kosigina, Moscow, 119334
N. Belikov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Ресей, 4 ul. Kosigina, Moscow, 119334
S. Varfolomeev
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Ресей, 4 ul. Kosigina, Moscow, 119334
A. Khodonov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
Ресей, 4 ul. Kosigina, Moscow, 119334
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