Pyrrolo[2,1-a]isoquinoline scaffold in drug discovery: Advances in synthesis and medicinal chemistry

Pyrrolo[2,1-a]isoquinoline (PIq) is a nitrogen heterocyclic scaffold of diverse alkaloids endowed with several biological activities, including antiretroviral and antitumor activities. Several 5,6-dihydro-PIq (DHPIq) alkaloids, belonging to the lamellarins' family, have proved to be cytotoxic to tumor cells, as well as reversers of multidrug resistance. In this review, we provide an overview of the main achievements over the last decade in the synthetic approaches to access libraries of PIq compounds along with a survey, as comprehensive as possible, of bioactivity, mechanism of action, pharmacophore and structure-activity relationships of synthetic analogs of DHPIq-based alkaloids. The focus is mainly on the potential exploitation of the (DH)PIq scaffold in design and development of novel antitumor drugs. © 2019 © 2019 Newlands Press.

Авторы
Matveeva M.D. 1 , Purgatorio R.2 , Voskressensky L.G. 1 , Altomare C.D.2
Издательство
NLM (Medline)
Номер выпуска
20
Язык
Английский
Страницы
2735-2755
Статус
Опубликовано
Том
11
Год
2019
Организации
  • 1 Department of Organic Chemistry, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 2 Department of Pharmacy-Drug Sciences, University of Bari Aldo Moro, Via E. Orabona 4, Bari, 70125, Italy
Ключевые слова
alkaloids; anticancer; antiviral; drug design; pharmacophore; pyrrolo[2,1-a]isoquinoline; structure-activity relationships; synthesis
Дата создания
24.12.2019
Дата изменения
24.12.2019
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/55314/
Поделиться

Другие записи