Natural Products and Drug Discovery

• Autore: Avato Pinarosa
• Pubblicazione: MDPI - Multidisciplinary Digital Publishing Institute, 2020
• Descrizione fisica: 1 online resource (392 p.)
• Soggetto topico: Biology, life sciences
• Soggetto non controllato: 2?; 4?-dihydroxy-6?-methoxy-3?; 5?-dimethylchalcone (DMC); ACE inhibitory peptide; acetylated astragalosides; aging; angiogenesis; anti-inflammatory activity; antihypertensive; antimicrobial agents; antimicrobial resistance; antinociceptive; antioxidant activity; artemisinin; Astragalus boeticus L.; Bacopa monnieri; bioactive peptides; bioactivities of natural products; biotechnology; C-glycoside; Ca2+; cancer; cardamonin; cardiovascular disease; celastrol; cerebellum; chemical derivatization; chemosystematics; chromatography; circular dichroism; Cleistocalyx operculatus; Cuba; cytokines; cytotoxic activity; cytotoxicity-guided; Dasycladus vermicularis; dementia; devil's claw; diabetes; diabetic neuropathy; dihydrochalcones; Dryopteris fragrans; Eruca sativa; ESI-MS/MS; Fabaceae; Fideloside; flavonoid; flavonoids; FSE; glucoerucin; glucosinolates; GLUT4; glutamate; growth inhibitory activity; H2S; Harpagophytum procumbens; harpagoside; HPLC; HPLC-ESI-microTOF-Q-MS/MS; human colon cancer cell lines; Humulus lupulus; hypertension; immuno-regulation activity; Imperata cylindrica; inflammation; isoflavones; isolation and quantification; ketamine; Kv7 potassium channels; L6 cell; Lamiales; LC-MS; Leea indica; Leishmania mexicana mexicana; malaria; marine peptides; marine resources; mass spectrometry; metabolomics; methicillin-resistant Staphylococcus aureus; migration; molecular network; multivariate data analysis; n/a; NADPH oxidases; natural products; neuropathic pain; NMR; opioid; Orobanchaceae; Orobanche s.l.; oxidative stress; PANC-1; phenolic derivatives; phenolics; phenylethanoid glycosides; phenylpropanoid glycosides; Phyllanthus chamacristoides; Phyllanthus orbicularis; Physcomitrella patens; pPancreatic cancer; prenylated phenolic compounds; proanthocyanidins; proliferation; psychosis; secondary metabolites; sesquiterpenoids; siphonous green algae; spagyric tincture; spectroscopic analysis; stereochemistry; sulfated coumarins; synergy; T2DM; terpenes; terpenoids; traditional medicine; Trifolium; TRPV1; Trypanosoma brucei brucei; zebrafish
• Sommario/riassunto: Natural products hold a prominent position in the current discovery and development of drugs and have diverse indications for both human and animal health. Plants, in particular, play a leading role as a source of specialized metabolites with medical effects. Other organisms, such as marine and terrestrial animals and microorganisms, produce very important drug candidate molecules. Specialized metabolites from these varied natural sources can be used directly as bioactive compounds or drug precursors. In addition, due to their broad chemical diversity, they can act as drug prototypes and/or be used as pharmacological tools for different targets. Some examples of natural metabolites that have been developed into useful medical drug are cardiotonic digoxin from Digitalis sp., antimalarial artemisinin from Artemisia annua, anti-cancer taxol from Taxus sp., or podophyllotoxin from Podophyllum peltatum, which served as a synthetic model for the anti-cancer etoposide. The study of natural products is still attracting great scientific attention and their current importance, as a valuable lead for drug discovery, is undebatable. I cordially invite authors to contribute original articles, as well as survey articles, that give the readers of Molecules **MOLECULES NEEDS TO BE ITALICIZED** updated and new perspectives on natural products in drug discovery, including but not limited to natural sources, identification and separation of bioactive phytochemicals, standardization, new biological targets, pre-clinical and clinical trials, pharmacological effects/side effects, and bioassays.
• Titolo autorizzato: Natural Products and Drug Discovery
• ISBN: 3-03928-747-8
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910404086803321
• Lo trovi qui: Univ. Federico II