3-Pyridylisoxazoles as prototypes of antiaggregatory agents
- 作者: Demina O.V.1, Belikov N.E.1, Varfolomeev S.D.1, Khodonov A.A.1
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隶属关系:
- N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
- 期: 卷 67, 编号 5 (2018)
- 页面: 866-877
- 栏目: 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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详细
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.
作者简介
O. Demina
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: ovd@sky.chph.ras.ru
俄罗斯联邦, 4 ul. Kosigina, Moscow, 119334
N. Belikov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
俄罗斯联邦, 4 ul. Kosigina, Moscow, 119334
S. Varfolomeev
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
俄罗斯联邦, 4 ul. Kosigina, Moscow, 119334
A. Khodonov
N. M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: ovd@sky.chph.ras.ru
俄罗斯联邦, 4 ul. Kosigina, Moscow, 119334
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