ChemInform Abstract: Syntheses of Bioactive Natural Products and Natural-Product-Like Compounds Based on Their Key Structural Units

ChemInform ◽  
2014 ◽  
Vol 45 (49) ◽  
pp. no-no
Author(s):  
Hongbin Zhang
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Structural Units ◽  
Bioactive Natural Products

scholarly journals Marine Rare Actinomycetes: A Promising Source of Structurally Diverse and Unique Novel Natural Products

Marine Drugs ◽  
2019 ◽  
Vol 17 (5) ◽  
pp. 249 ◽  
Author(s):  
Subramani ◽  
Sipkema
Keyword(s):  
Natural Products ◽  
New Species ◽  
Secondary Metabolites ◽  
Natural Product ◽  
Bioactive Compounds ◽  
Marine Environment ◽  
Present Knowledge ◽  
Bioactive Natural Products ◽  
Rare Actinomycetes ◽  
Promising Source

Rare actinomycetes are prolific in the marine environment; however, knowledge about their diversity, distribution and biochemistry is limited. Marine rare actinomycetes represent a rather untapped source of chemically diverse secondary metabolites and novel bioactive compounds. In this review, we aim to summarize the present knowledge on the isolation, diversity, distribution and natural product discovery of marine rare actinomycetes reported from mid-2013 to 2017. A total of 97 new species, representing 9 novel genera and belonging to 27 families of marine rare actinomycetes have been reported, with the highest numbers of novel isolates from the families Pseudonocardiaceae, Demequinaceae, Micromonosporaceae and Nocardioidaceae. Additionally, this study reviewed 167 new bioactive compounds produced by 58 different rare actinomycete species representing 24 genera. Most of the compounds produced by the marine rare actinomycetes present antibacterial, antifungal, antiparasitic, anticancer or antimalarial activities. The highest numbers of natural products were derived from the genera Nocardiopsis, Micromonospora, Salinispora and Pseudonocardia. Members of the genus Micromonospora were revealed to be the richest source of chemically diverse and unique bioactive natural products.

scholarly journals Zebrafish as an Emerging Model for Bioassay-Guided Natural Product Drug Discovery for Neurological Disorders

Medicines ◽  
2019 ◽  
Vol 6 (2) ◽  
pp. 61 ◽  
Author(s):  
Arjun Pitchai ◽  
Rajesh Kannan Rajaretinam ◽  
Jennifer L. Freeman
Keyword(s):  
Natural Products ◽  
Drug Discovery ◽  
Natural Product ◽  
Neurological Disorders ◽  
Experimental Models ◽  
Bioactive Natural Products ◽  
Natural Product Research ◽  
Model Platform

Most neurodegenerative diseases are currently incurable, with large social and economic impacts. Recently, there has been renewed interest in investigating natural products in the modern drug discovery paradigm as novel, bioactive small molecules. Moreover, the discovery of potential therapies for neurological disorders is challenging and involves developing optimized animal models for drug screening. In contemporary biomedicine, the growing need to develop experimental models to obtain a detailed understanding of malady conditions and to portray pioneering treatments has resulted in the application of zebrafish to close the gap between in vitro and in vivo assays. Zebrafish in pharmacogenetics and neuropharmacology are rapidly becoming a widely used organism. Brain function, dysfunction, genetic, and pharmacological modulation considerations are enhanced by both larval and adult zebrafish. Bioassay-guided identification of natural products using zebrafish presents as an attractive strategy for generating new lead compounds. Here, we see evidence that the zebrafish’s central nervous system is suitable for modeling human neurological disease and we review and evaluate natural product research using zebrafish as a vertebrate model platform to systematically identify bioactive natural products. Finally, we review recently developed zebrafish models of neurological disorders that have the potential to be applied in this field of research.

Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products

2015 ◽  
Vol 32 (4) ◽  
pp. 605-632 ◽  
Author(s):  
Michail Tsakos ◽  
Eva S. Schaffert ◽  
Lise L. Clement ◽  
Nikolaj L. Villadsen ◽  
Thomas B. Poulsen
Keyword(s):  
Natural Products ◽  
Chemical Synthesis ◽  
Natural Product ◽  
Organic Synthesis ◽  
State Of The Art ◽  
The State ◽  
Coupling Reactions ◽  
Total Syntheses ◽  
Bioactive Natural Products ◽  
Complex Ester

In this review we investigate the use of complex ester fragment couplings within natural product total syntheses. Using examples from the literature up to 2014 we illustrate the state-of-the-art as well as the challenges within this area of organic synthesis.

scholarly journals The Curtius rearrangement: mechanistic insight and recent applications in natural product syntheses

2018 ◽  
Vol 16 (12) ◽  
pp. 2006-2027 ◽  
Author(s):  
Arun K. Ghosh ◽  
Anindya Sarkar ◽  
Margherita Brindisi
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Extensive Review ◽  
Curtius Rearrangement ◽  
Bioactive Natural Products ◽  
Mechanistic Insight ◽  
Curtius Reaction

An extensive review on the Curtius reaction and its recent applications in the synthesis of bioactive natural products are reported.

scholarly journals Discovery of Novel Glycerolated Quinazolinones from Streptomyces sp. MBT27

2018 ◽  
Author(s):  
Nataliia Machushynets ◽  
Changsheng Wu ◽  
Somayah S. Elsayed ◽  
Thomas Hankemeier ◽  
Gilles P. van Wezel
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Secondary Metabolite ◽  
Anthranilic Acid ◽  
Growth Conditions ◽  
Secondary Metabolite Production ◽  
Streptomyces Sp ◽  
Metabolite Production ◽  
Bioactive Natural Products ◽  
Interesting Family

AbstractActinobacteria are a major source of novel bioactive natural products. A challenge in the screening of these microorganisms lies in finding the favorable growth conditions for secondary metabolite production and dereplication of known molecules. Here, we report that Streptomyces sp. MBT27 produces 4-quinazolinone alkaloids in response to elevated levels of glycerol, whereby quinazolinones A (1) and B (2) form a new sub-class of this interesting family of natural products. Global Natural Product Social molecular networking (GNPS) resulted in a quinazolinone-related network that included anthranilic acid (3), anthranilamide (4), 4(3H)-quinazolinone (5) and 2,2-dimethyl-1,2-dihydroquinazolin-4(3H)-one (6). Actinomycins D (7) and X2 (8) were also identified in the extracts of Streptomyces sp. MBT27. The induction of quinazolinone production by glycerol combined with biosynthetic insights provide evidence that glycerol is integrated into the chemical scaffold. The unprecedented 1,4-dioxepane ring that is spiro-fused into the quinazolinone backbone, is most likely formed by intermolecular etherification of two units of glycerol. Our work underlines the importance of varying the growth conditions for the discovery of novel natural products and for understanding their biosynthesis.

Cycloaddition/annulation strategies for the construction of multisubstituted pyrrolidines and their applications in natural product synthesis

2018 ◽  
Vol 5 (5) ◽  
pp. 864-892 ◽  
Author(s):  
Jundong Li ◽  
Yilin Ye ◽  
Yandong Zhang
Keyword(s):  
Natural Products ◽  
Natural Product ◽  
Natural Product Synthesis ◽  
Bioactive Natural Products

Pyrrolidines are privileged substructures of numerous bioactive natural products and drugs.

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