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U.S. FDA Approved Drugs from 2015–June 2020: A Perspective

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dc.contributor.author Paul, Atish Tulshiram
dc.date.accessioned 2023-12-27T08:58:20Z
dc.date.available 2023-12-27T08:58:20Z
dc.date.issued 2021
dc.identifier.uri https://pubs.acs.org/doi/full/10.1021/acs.jmedchem.0c01786
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13536
dc.description.abstract In the present work, we report compilation and analysis of 245 drugs, including small and macromolecules approved by the U.S. FDA from 2015 until June 2020. Nearly 29% of the drugs were approved for the treatment of various types of cancers. Other major therapeutic areas of focus were infectious diseases (14%); neurological conditions (12%); and genetic, metabolic, and cardiovascular disorders (7–8% each). Itemization of the approved drugs according to the year of approval, sponsor, target, chemical class, major drug-metabolizing enzyme(s), route of administration/elimination, and drug–drug interaction liability (perpetrator or/and victim) is presented and discussed. An effort has been made to analyze the pharmacophores to identify the structural (e.g., aromatic, heterocycle, and aliphatic), elemental (e.g., boron, sulfur, fluorine, phosphorus, and deuterium), and functional group (e.g., nitro drugs) diversity among the approved drugs. Further, descriptor-based chemical space analysis of FDA approved drugs and several strategies utilized for optimizing metabolism leading to their discoveries have been emphasized. Finally, an analysis of drug-likeness for the approved drugs is presented. en_US
dc.language.iso en en_US
dc.publisher ACS en_US
dc.subject Pharmacy en_US
dc.subject Drug en_US
dc.subject Neurological disorders en_US
dc.title U.S. FDA Approved Drugs from 2015–June 2020: A Perspective en_US
dc.type Article en_US


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