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      Role of pharmaceutical sciences in future drug discovery

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          Abstract

          The recent emergence of COVID-19 influenced the layman’s knowledge of drugs. Although several drugs have been discovered serendipitously, research has moved to the next-generation era of drug discovery. The use of drugs is inevitable and they have become lifesavers in the present era. Although research from different scientific backgrounds has supported the translational research of drug discovery, the prime role of pharmacy has to be remembered. Here we have summarized the role of some important subjects in pharmacy education, which have paved different ways in drug discovery and development.

          Lay abstract

          Despite existing therapies for various ailments, emerging diseases or disorders need more selective treatments. Traditionally ‘pharmacy’ is thought of as a medical store, but time has changed pharmacy into a multidisciplinary subject with core research domains, including pharmacognosy, pharmaceutical biotechnology, pharmaceutical analysis, pharmaceutical chemistry, pharmacology and pharmaceutics. The main objective of these subjects is to provide strong support for both basic and translational research. Here we summarize the role of each of these domains of pharmaceutical science in the design and development of pharmaceuticals.

          Tweetable abstract

          How pharmacy’s core research domains provide strong support for both basic and translational drug discovery research.

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          Most cited references45

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          Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019

          This review is an updated and expanded version of the five prior reviews that were published in this journal in 1997, 2003, 2007, 2012, and 2016. For all approved therapeutic agents, the time frame has been extended to cover the almost 39 years from the first of January 1981 to the 30th of September 2019 for all diseases worldwide and from ∼1946 (earliest so far identified) to the 30th of September 2019 for all approved antitumor drugs worldwide. As in earlier reviews, only the first approval of any drug is counted, irrespective of how many "biosimilars" or added approvals were subsequently identified. As in the 2012 and 2016 reviews, we have continued to utilize our secondary subdivision of a "natural product mimic", or "NM", to join the original primary divisions, and the designation "natural product botanical", or "NB", to cover those botanical "defined mixtures" now recognized as drug entities by the FDA (and similar organizations). From the data presented in this review, the utilization of natural products and/or synthetic variations using their novel structures, in order to discover and develop the final drug entity, is still alive and well. For example, in the area of cancer, over the time frame from 1946 to 1980, of the 75 small molecules, 40, or 53.3%, are N or ND. In the 1981 to date time frame the equivalent figures for the N* compounds of the 185 small molecules are 62, or 33.5%, though to these can be added the 58 S* and S*/NMs, bringing the figure to 64.9%. In other areas, the influence of natural product structures is quite marked with, as expected from prior information, the anti-infective area being dependent on natural products and their structures, though as can be seen in the review there are still disease areas (shown in Table 2) for which there are no drugs derived from natural products. Although combinatorial chemistry techniques have succeeded as methods of optimizing structures and have been used very successfully in the optimization of many recently approved agents, we are still able to identify only two de novo combinatorial compounds (one of which is a little speculative) approved as drugs in this 39-year time frame, though there is also one drug that was developed using the "fragment-binding methodology" and approved in 2012. We have also added a discussion of candidate drug entities currently in clinical trials as "warheads" and some very interesting preliminary reports on sources of novel antibiotics from Nature due to the absolute requirement for new agents to combat plasmid-borne resistance genes now in the general populace. We continue to draw the attention of readers to the recognition that a significant number of natural product drugs/leads are actually produced by microbes and/or microbial interactions with the "host from whence it was isolated"; thus we consider that this area of natural product research should be expanded significantly.
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            The re-emergence of natural products for drug discovery in the genomics era.

            Natural products have been a rich source of compounds for drug discovery. However, their use has diminished in the past two decades, in part because of technical barriers to screening natural products in high-throughput assays against molecular targets. Here, we review strategies for natural product screening that harness the recent technical advances that have reduced these barriers. We also assess the use of genomic and metabolomic approaches to augment traditional methods of studying natural products, and highlight recent examples of natural products in antimicrobial drug discovery and as inhibitors of protein-protein interactions. The growing appreciation of functional assays and phenotypic screens may further contribute to a revival of interest in natural products for drug discovery.
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              Microbial drug discovery: 80 years of progress

              Microbes have made a phenomenal contribution to the health and well-being of people throughout the world. In addition to producing many primary metabolites, such as amino acids, vitamins and nucleotides, they are capable of making secondary metabolites, which constitute half of the pharmaceuticals on the market today and provide agriculture with many essential products. This review centers on these beneficial secondary metabolites, the discovery of which goes back 80 years to the time when penicillin was discovered by Alexander Fleming.
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                Author and article information

                Journal
                FDD
                Future Drug Discovery
                Future Drug. Discov.
                Future Drug Discovery
                Newlands Press Ltd (London, UK )
                2631-3316
                18 October 2021
                September 2021
                : 3
                : 3
                : FDD64
                Affiliations
                1Institute National de la Santé et de la Recherche Médicale, Centre de Recherche des Cordeliers, Equipe-Immunopathologie et Immunointervention Thérapeutique, Sorbonne Université, Université de Paris, Paris, F-75006, France
                2Department of Pharmaceutical Chemistry, Faculty of Pharmacy & Health Sciences, University Kuala Lumpur Royal College of Medicine Perak, Ipoh, 30450, Perak, Malaysia
                3Department of Pharmaceutical Biotechnology, Andhra University College of Pharmaceutical Sciences, Andhra University, Visakhapatnam, 530003, Andhra Pradesh, India
                4Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA
                5Department of Pharmaceutical Analysis, Andhra University College of Pharmaceutical Sciences, Andhra University, Visakhapatnam, 530003, Andhra Pradesh, India
                6Department of Cancer Biology & Pharmacology, University of Illinois College of Medicine at Peoria, 1 Illini Dr, Peoria, IL 61605, USA
                7Department of Pharmacology, KVSR Siddhartha College of Pharmaceutical Sciences, Vijayawada, 520010, Andhra Pradesh, India
                8Department of Pharmaceutics, Bapatla College of Pharmacy, Bapatla, Guntur, 522101, Andhra Pradesh, India
                9House of the Provinces of France, Paris, 75014, France
                Author notes
                [* ]Author for correspondence: bsrpharmacy90@ 123456gmail.com
                Author information
                https://orcid.org/0000-0002-2888-2418
                https://orcid.org/0000-0002-3022-6137
                https://orcid.org/0000-0002-0491-5377
                https://orcid.org/0000-0002-0132-9516
                https://orcid.org/0000-0003-0487-2757
                https://orcid.org/0000-0002-4389-5567
                https://orcid.org/0000-0002-8017-0522
                Article
                10.4155/fdd-2021-0005
                4e1460e2-f4a8-4f1f-af29-6e19e90bfb28
                © 2021 Srinivasa Reddy Bonam

                This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License

                History
                : 28 June 2021
                : 20 September 2021
                : 18 October 2021
                Page count
                Pages: 15
                Funding
                Funded by: Ministry of Higher Education, Malaysia
                Award ID: FRGS/1/2018/SKK10/UNIKL/02/1
                Categories
                Special Report

                Biochemistry,Molecular medicine,Pharmaceutical chemistry,Bioinformatics & Computational biology,Biotechnology,Pharmacology & Pharmaceutical medicine
                pharmacognosy,pharmaceutical research,pharmaceutical analysis,pharmacology,pharmaceutical biotechnology,statistics,pharmaceutical chemistry,bioinformatics,pharmaceutical engineering,pharmaceutics,drug discovery and development,pharmacy

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