A convenient synthesis of cis-restricted combretastatin analogues with pyrazole and isoxazole cores Научная публикация
| Журнал |
Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Вых. Данные | Год: 2019, Том: 29, Номер: 2, Страницы: 163-165 Страниц : 3 DOI: 10.1016/j.mencom.2019.03.015 | ||||
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Реферат:
A series of combretastatin analogues, diarylpyrazoles and diarylisoxazoles, have been synthesized and evaluated for their antimitotic tubulin-binding activity using the phenotypic sea urchin (Paracentrotus lividus) embryo assay. One pyrazole analogue and four isoxazole analogues have been identified as potent antimitotic agents comparable with combretastatins A-2 and A-4, with the lowest observable effective concentration of 1–10 nmol dm−3 for cleavage alteration of the test embryos.
Библиографическая ссылка:
Tsyganov D.V.
, Semenova M.N.
, Konyushkin L.D.
, Ushkarov V.I.
, Raihstat M.M.
, Semenov V.V.
A convenient synthesis of cis-restricted combretastatin analogues with pyrazole and isoxazole cores
Mendeleev Communications. 2019. V.29. N2. P.163-165. DOI: 10.1016/j.mencom.2019.03.015 WOS Scopus OpenAlex
A convenient synthesis of cis-restricted combretastatin analogues with pyrazole and isoxazole cores
Mendeleev Communications. 2019. V.29. N2. P.163-165. DOI: 10.1016/j.mencom.2019.03.015 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000467509600015 |
| Scopus: | 2-s2.0-85058076699 |
| OpenAlex: | W2939541223 |