Literature DB >> 20704903

Rediscovering natural products as a source of new drugs.

Frank E Koehn1, Guy T Carter.   

Abstract

Extract: Since the very beginnings of human medicine, physicians have relied on chemical compounds produced by animals, plants and microorganisms, so-called natural products, to treat diseases. Natural products are directly or indirectly responsible for roughly one-half of all drugs currently in use. Of the 877 small-molecule new drug molecules introduced between 1981 and 2002, 49% were natural products or natural product analogs. Despite the great success of the 70s and 80s, the pharmaceutical industry de-emphasized natural products research during the following decade. In this article, we examine the underlying reasons for the decline, and assess future prospects for natural products research in drug discovery. In the 1990s, major pharmaceutical companies moved to a lead-finding strategy based on High Throughput Screening (HTS) of very large collections (libraries) of synthetic compounds. The move arose from the belief that techniques such as combinatorial chemistry could produce larger, more cost-effective libraries with improved hit rates and quality. Additionally, advances in molecular biology, cellular biology and genomics dramatically increased the number of molecular targets, prompting shorter drug discovery timelines. In today's drug discovery environment, rapid screening and identification of potential drug molecules is essential for success. This puts traditional natural products-based programs, with their reliance on the lengthy processes of the screening of extracts library, bioassay-guided isolation of the active components, structure elucidation and subsequent production scale-up, at a competitive disadvantage.

Entities:  

Year:  2005        PMID: 20704903

Source DB:  PubMed          Journal:  Discov Med        ISSN: 1539-6509            Impact factor:   2.970


  13 in total

1.  Titration-based screening for evaluation of natural product extracts: identification of an aspulvinone family of luciferase inhibitors.

Authors:  Patricia G Cruz; Douglas S Auld; Pamela J Schultz; Scott Lovell; Kevin P Battaile; Ryan MacArthur; Min Shen; Giselle Tamayo-Castillo; James Inglese; David H Sherman
Journal:  Chem Biol       Date:  2011-11-23

2.  Exploring the diversity and metabolic potential of actinomycetes from temperate marine sediments from Newfoundland, Canada.

Authors:  K R Duncan; B Haltli; K A Gill; H Correa; F Berrué; R G Kerr
Journal:  J Ind Microbiol Biotechnol       Date:  2014-11-05       Impact factor: 3.346

3.  Hydrogenosome metabolism is the key target for antiparasitic activity of resveratrol against Trichomonas vaginalis.

Authors:  Natalia Mallo; Jesús Lamas; José M Leiro
Journal:  Antimicrob Agents Chemother       Date:  2013-03-11       Impact factor: 5.191

4.  Bioprospecting from marine sediments of New Brunswick, Canada: exploring the relationship between total bacterial diversity and actinobacteria diversity.

Authors:  Katherine Duncan; Bradley Haltli; Krista A Gill; Russell G Kerr
Journal:  Mar Drugs       Date:  2014-02-13       Impact factor: 5.118

5.  Natural antimicrobial peptides as promising anti-HIV candidates.

Authors:  Guangshun Wang
Journal:  Curr Top Pept Protein Res       Date:  2012

6.  Digital marine bioprospecting: mining new neurotoxin drug candidates from the transcriptomes of cold-water sea anemones.

Authors:  Ilona Urbarova; Bård Ove Karlsen; Siri Okkenhaug; Ole Morten Seternes; Steinar D Johansen; Åse Emblem
Journal:  Mar Drugs       Date:  2012-10-18       Impact factor: 6.085

Review 7.  Targeting apoptosis pathways in cancer with alantolactone and isoalantolactone.

Authors:  Azhar Rasul; Muhammad Khan; Muhammad Ali; Jiang Li; Xiaomeng Li
Journal:  ScientificWorldJournal       Date:  2013-10-27

8.  Database-Guided Discovery of Potent Peptides to Combat HIV-1 or Superbugs.

Authors:  Guangshun Wang
Journal:  Pharmaceuticals (Basel)       Date:  2013-05-27

Review 9.  Synthetic biology for pharmaceutical drug discovery.

Authors:  Jean-Yves Trosset; Pablo Carbonell
Journal:  Drug Des Devel Ther       Date:  2015-12-03       Impact factor: 4.162

10.  Histone deacetylase inhibitor thailandepsin-A activates Notch signaling and suppresses neuroendocrine cancer cell growth in vivo.

Authors:  Samuel Jang; Andrew Janssen; Zviadi Aburjania; Matthew B Robers; April Harrison; Ajitha Dammalapati; Yi-Qiang Cheng; Herbert Chen; Renata Jaskula-Sztul
Journal:  Oncotarget       Date:  2017-08-07
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