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Structural diversity and chemical logic underlying the assembly of monoterpene indole alkaloids oligomers.
- Source :
-
Natural Product Reports . Nov2024, Vol. 41 Issue 11, p1723-1765. 43p. - Publication Year :
- 2024
-
Abstract
- Covering: up to 2024 This review aims to draw a parallel between all known oligomers of monoterpene indole alkaloids (MIAs) by illustrating the chemical logic underlying their assembly. For this purpose, oligomeric MIAs were first comprehensively listed and organized according to the names of the backbones of their constitutive monomers and the binding sites. From this extensive list, an oligomer network was generated and unprecedented MIA statistics were mined and shared herein. Subsequently, oligomeric MIAs were categorized according to the number of connections instigated between their monomeric components (single, double, triple, and mixed tethering), then subdivided according to the uniqueness or combination of oligomerization assembly reactions. This effort outlined oligomerization trends in a scaffold-specific manner, and established binding reactivity patterns facilitating the comprehension of the associated biosynthetic processes. At last, this review illustrates a unique initiative in crafting a comprehensive repository of machine-readable metadata for MIA oligomers that could be leveraged for chemoinformatic purposes. [ABSTRACT FROM AUTHOR]
- Subjects :
- *INDOLE alkaloids
*BINDING sites
*OLIGOMERS
*OLIGOMERIZATION
*MONOMERS
Subjects
Details
- Language :
- English
- ISSN :
- 02650568
- Volume :
- 41
- Issue :
- 11
- Database :
- Academic Search Index
- Journal :
- Natural Product Reports
- Publication Type :
- Academic Journal
- Accession number :
- 180820243
- Full Text :
- https://doi.org/10.1039/d4np00011k