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Open AccessJournal ArticleDOI

Chemical Diversity and Bioactivities of Monoterpene Indole Alkaloids (MIAs) from Six Apocynaceae Genera

TLDR
In this paper, a review of Indole Alkaloids from six genera belonging to the family Apocynaceae is presented, and the genera (Alstonia, Rauvolfia, Kopsia, Ervatamia, and Tabernaemontana, and Rhazya) consist of 400 members and represent 20% of the species.
Abstract
By the end of the twentieth century, the interest in natural compounds as probable sources of drugs has declined and was replaced by other strategies such as molecular target-based drug discovery. However, in the recent times, natural compounds regained their position as extremely important source drug leads. Indole-containing compounds are under clinical use which includes vinblastine and vincristine (anticancer), atevirdine (anti-HIV), yohimbine (erectile dysfunction), reserpine (antihypertension), ajmalicine (vascular disorders), ajmaline (anti-arrhythmic), vincamine (vasodilator), etc. Monoterpene Indole Alkaloids (MIAs) deserve the curiosity and attention of researchers due to their chemical diversity and biological activities. These compounds were considered as an impending source of drug-lead. In this review 444 compounds, were identified from six genera belonging to the family Apocynaceae, will be discussed. These genera (Alstonia, Rauvolfia, Kopsia, Ervatamia, and Tabernaemontana, and Rhazya) consist of 400 members and represent 20% of Apocynaceae species. Only 30 (7.5%) species were investigated, whereas the rest are promising to be investigated. Eleven bioactivities, including antibacterial, antifungal, anti-inflammatory and immunosuppressant activities, were reported. Whereas cytotoxic effect represents 47% of the reported activities. Convincingly, the genera selected in this review are a wealthy source for future anticancer drug lead.

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Citations
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Construction of ajmalicine and sanguinarine de novo biosynthetic pathways using stable integration sites in yeast

TL;DR: This work profiles genomic loci flanked by essential genes as stable integration sites in a genome‐wide manner, for stable maintenance of multigene biosynthetic pathways in yeast, and establishes stable yeast cell factories that can produce 119.2 mg L−1 heteroyohimbine alkaloids in shake flasks.
Journal ArticleDOI

Bisindole Alkaloids from the Alstonia Species: Recent Isolation, Bioactivity, Biosynthesis, and Synthesis.

TL;DR: In this article, the isolation of bisindoles from various Alstonia species, their bioactivity, putative biosynthesis, and synthesis are discussed, as well as the partial synthesis of alstonisidine, villalstonine, and macrocarpamine.
Journal ArticleDOI

Isolation and biological activity of azocine and azocane alkaloids

TL;DR: The structure and bioactivity of alkaloids that contain an azocine (or saturated azocane) ring and the array of sources whence they originate are discussed in this article .
References
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Journal ArticleDOI

Biomedical Importance of Indoles

TL;DR: Some of the relevant and recent achievements in the biological, chemical and pharmacological activity of important indole derivatives in the areas of drug discovery and analysis are covered.
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Chemistry and biology of monoterpene indole alkaloid biosynthesis

TL;DR: The biosynthetic pathways for several representative terpene indole alkaloids are described in detail, showing a diverse array of structures and biological activities.
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A revised classification of the Apocynaceae s.l.

TL;DR: A unified classification for the Apocynaceae is provided, which consists of 424 genera distributed among five subfamilies and tribes, with lists of genera that (as far as the authors have been able to ascertain) are recognized in each tribe.
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A uniform numbering system for indole alkaloids.

TL;DR: Nous proposons un mode uniforme de numérotation pour le squelette des alcaloïdes indoliques complexes complexes d'être coupés en éléments identiques.
Journal ArticleDOI

Catharanthus terpenoid indole alkaloids: biosynthesis and regulation

TL;DR: Most of the work focussed on early steps of the pathway, particularly the discovery of the 2-C-methyl-d-erythritol 4-phosphate (MEP)-pathway leading to terpenoids, and much progress has been made at alkaloid regulatory level.
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