Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
Marine natural products are characterized by high chemical diversity, biochemical specificity, and other molecular properties that make them favorable as lead structures for drug discovery. In this field, one of the main problems is often the reduced natural availability of isolated substances, whic...
Format: | eBook |
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Language: | English |
Published: |
Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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Online Access: | Open Access: DOAB: description of the publication Open Access: DOAB, download the publication |
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020 | |a 9783036517674 | ||
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042 | |a dc | ||
072 | 7 | |a C |2 bicssc | |
720 | 1 | |a Manzo, Emiliano |4 edt | |
720 | 1 | |a Manzo, Emiliano |4 oth | |
245 | 0 | 0 | |a Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances |
260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2021 | ||
300 | |a 1 online resource (147 p.) | ||
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520 | |a Marine natural products are characterized by high chemical diversity, biochemical specificity, and other molecular properties that make them favorable as lead structures for drug discovery. In this field, one of the main problems is often the reduced natural availability of isolated substances, which can complicate both the structural characterization and possible future developments. For these reasons, the study of bioactive marine metabolites should rely on the development of chemical synthesis and synthetic strategies aimed at the preparation of pure compounds and analogs both for structural confirmation and/or for the large-scale preparation necessary for future applications. Moreover, natural products can be a crucial starting point for the preparation of molecules structurally inspired by the latter, opening the path to new classes of biologically active compounds with pharmacological potential. This book collects original research articles regarding synthetic strategies for secondary marine metabolites and/or analogs that favor applications of these molecules and/or solve structural challenges common in the field of natural substances. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |u https://creativecommons.org/licenses/by/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Language and Linguistics |2 bicssc | |
653 | |a 7-deazapurine nucleoside | ||
653 | |a alkylglycerol (AKG) | ||
653 | |a amides/esters | ||
653 | |a antibacterial iminosugars | ||
653 | |a antibiotics (gentamicin | ||
653 | |a antimicrobial activity | ||
653 | |a antiproliferative activity | ||
653 | |a apoptosis | ||
653 | |a aureol | ||
653 | |a bioactive diterpenes | ||
653 | |a bis-indoles | ||
653 | |a breast cancer | ||
653 | |a carbohydrates | ||
653 | |a cholesterol | ||
653 | |a ciprofloxacin and ampicillin) | ||
653 | |a COVID-19 | ||
653 | |a cytostatic | ||
653 | |a disaccharide nucleoside | ||
653 | |a fluoro olefin | ||
653 | |a fucose | ||
653 | |a fucosylated chondroitin sulfate | ||
653 | |a G0/G1 cell-cycle arrest | ||
653 | |a glycosylation | ||
653 | |a HDAC inhibitors | ||
653 | |a labdane scaffold | ||
653 | |a largazole | ||
653 | |a lipophilic iminosugars | ||
653 | |a marine natural product | ||
653 | |a marine-inspired | ||
653 | |a meroterpenoids | ||
653 | |a modification | ||
653 | |a n/a | ||
653 | |a natural product | ||
653 | |a natural products synthesis | ||
653 | |a organic synthesis | ||
653 | |a polymer-supported triphenyl phosphine | ||
653 | |a polysaccharides | ||
653 | |a ricinoleic acid (RA) | ||
653 | |a SARS-CoV-2 | ||
653 | |a sclareolide | ||
653 | |a semi-synthesis | ||
653 | |a solid tumor cell lines | ||
653 | |a structure-activity relationship (SAR) studies | ||
653 | |a structure-activity relationships | ||
653 | |a sulfation | ||
653 | |a synthesis | ||
653 | |a tetracyclic meroterpenoids | ||
653 | |a tetracycline | ||
653 | |a thiazinoquinones | ||
653 | |a total synthesis | ||
653 | |a TRPV4 channel | ||
653 | |a tubercidin | ||
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