New Strategies for Natural Products Lead Generation

Author(s):  
Guy T. Carter ◽  
Valerie S. Bernan ◽  
Frank E. Koehn
2020 ◽  
Vol 53 (11) ◽  
pp. 2569-2586
Author(s):  
Weilong Liu ◽  
Benke Hong ◽  
Jin Wang ◽  
Xiaoguang Lei

2014 ◽  
Vol 60 (3) ◽  
pp. 147-154 ◽  
Author(s):  
Gerard D. Wright

Antibiotic discovery is in crisis. Despite a growing need for new drugs resulting from the increasing number of multi-antibiotic-resistant pathogens, there have been only a handful of new antibiotics approved for clinical use in the past 2 decades. Faced with scientific, economic, and regulatory challenges, the pharmaceutical sector seems unable to respond to what has been called an “apocalyptic” threat. Natural products produced by bacteria and fungi are genetically encoded products of natural selection that have been the mainstay sources of the antibiotics in current clinical use. The pharmaceutical industry has largely abandoned these compounds in favor of large libraries of synthetic molecules because of difficulties in identifying new natural product antibiotics scaffolds. Advances in next-generation genome sequencing, bioinformatics, and analytical chemistry are combining to overcome barriers to natural products. Coupled with new strategies in antibiotic discovery, including inhibition of resistance, novel drug combinations, and new targets, natural products are poised for a renaissance to address what is a pressing health care crisis.


2005 ◽  
Vol 77 (1) ◽  
pp. 1-6 ◽  
Author(s):  
H. Wagner

The gradual transition from the long-standing use of monodrug therapy in classical medicine to the new concept of a multidrug and multitarget therapy has great implications for the research strategies of natural products chemistry and phytomedicine. The rationalization of the new strategies, however, requires great efforts in: standardization of mono- and multiphytopreparations using all available high-tech methods; screening of extracts and their constituents by integration of modern molecular biological bioassays; and controlled, clinical studies, inclusive of pharmacokinetic and bioavailability investigations, aimed at evidence-based phytotherapy. The first results obtained in recent years are explained using several examples of phytopharmacological and clinical studies. These show the therapeutic superiority of many plant extracts over single isolated constituents, as well as the bioequivalence of many phytopharmaceuticals with synthetic chemotherapeutics.


2017 ◽  
Vol 48 ◽  
pp. 21-27 ◽  
Author(s):  
Hengqian Ren ◽  
Bin Wang ◽  
Huimin Zhao

2019 ◽  
Vol 20 (12) ◽  
pp. 1218-1225 ◽  
Author(s):  
Rajeev K. Singla ◽  
Rishabh Kumar ◽  
Sameer Khan ◽  
Mohit ◽  
Kajal Kumari ◽  
...  

Out of multiple therapeutic targets, DPP-IV is the lead target for the treatment of type 2 diabetes. Natural products have always been available for the possible lead generation against various diseases and disorders. In the present review, we have covered various natural sources which have experimentally validated anti-diabetic activity for type 2 diabetic patients with specific focus on the DPP-IV inhibition. Out of all, the most potent DPP-IV inhibitors were found to be resveratrol, luteolin, apigenin and flavone having activity in nanomolar range. Standard drugs like sitagliptin, saxagliptin, and diprotin A have complex structures as compared to these phenolic compounds. Flavonoids and phenolic compounds have their added advantages in being present in a number of functional foods and carry antioxidant properties as well. So, the scientists working on the new chemical entity hunting for the type 2 diabetes treatment can also explore these natural sources for lead generation.


Author(s):  
Beth A Lorsbach ◽  
Thomas C Sparks ◽  
Robert M Cicchillo ◽  
Negar V Garizi ◽  
Donald R Hahn ◽  
...  

2012 ◽  
Vol 84 (7) ◽  
pp. 1621-1631 ◽  
Author(s):  
Jason C. Green ◽  
G. Leslie Burnett ◽  
Thomas R. R. Pettus

Two cycloaddition strategies are described that lead to various chroman spiroketals from assorted exocyclic enol ethers. Unlike conventional thermodynamic ketalization strategies, the stereochemical outcome for this approach is determined by a kinetic cycloaddition reaction. Thus, the stereochemical outcome reflects the olefin geometry of the starting materials along with the orientation of the associated transition state. However, the initial kinetic product can also be equilibrated by acid catalysis and reconstituted into a thermodynamic stereochemical arrangement. Thus, these strategies uniquely enable synthetic access to either the thermodynamic or kinetic conformation of the spiroketal stereocenter itself. Applications of these strategies in the syntheses of berkelic acid, β-rubromycin, and paecilospirone are presented along with the use of a chroman spiroketal for the construction of heliespirones A and C.


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