Reprint
Terpenes and Terpene Derivatives
Edited by
October 2021
238 pages
- ISBN978-3-0365-2135-0 (Hardback)
- ISBN978-3-0365-2136-7 (PDF)
This is a Reprint of the Special Issue Terpenes and Terpene Derivatives that was published in
Chemistry & Materials Science
Medicine & Pharmacology
Summary
The book comprises selected communications on terpenes and terpene derivatives. It clearly demonstrates the sustained interest and importance in this field of natural products; the field connected to secondary metabolites; and renewable resources of plant and animal compounds for medicinal, material, supramolecular, and general chemistry research.
It includes 17 papers, 5 review articles, and 12 research communications with a vast range of topics with different perspectives. It commemorates the great work and legacy of prof. Kenji Mori, and provides important material not only to many chemists but also to specialists in several other fields.
Format
- Hardback
License and Copyright
© 2022 by the authors; CC BY-NC-ND license
Keywords
Junceella fragilis; fragilide; briarane; superoxide anion; betulin; osteoblasts; differentiation; mineralization; betulinic acid; structural modification; supramolecular self-assembly; cytotoxicity; antitumor activity; antiviral activity; physicochemical parameters; ADME parameters; quantitative nuclear magnetic resonance; high-throughput screening; resin acids; diterpenes; Pinus nigra; provenances; resins; limonene; triterpenes; microsamples; capillary liquid chromatography (Cap-LC); Lonicera macranthoides; Caprifoliaceae; Prenyleudesmanes; Hexanortriterpenes; Antiproliferative; Sideritis hyssopifolia; ent-kaurane; anti-inflammatory; NMR; Zingiberaceae; essential oil; terpene; cytotoxicity; embryotoxicity; zebrafish; Anvillea garcinii; Saudi medicinal plants; sesquiterpene lactones; antifungal activity; Lindera; sesquiterpene; lindenane; DFT-NMR; rearrangement reactions; sesquiterpenes; sesquiterpene lactones; conjugation; metabolic engineering; enzyme characterization; transannular cyclization; Cope rearrangement; Rubiaceae; iridoids; bis-iridoids; Lasianthus verticillatus; lasianoside; lycopene; the MEP pathway; the MVA pathway; Escherichia coli; metabolic engineering; uvaol; terpenes medicinal; wound healing; fibroblasts; endothelial cells; FRAP; terpenes; antioxidant; steroid saponin; diosgenin glycosides; diosgenyl β-d-glucosaminoside; diosgenyl β-d-galactosaminoside; amine group modifications; antimicrobial activity; anti-cancer activity; hemolytic activity; terpenes; terpenoids; lipid nanoparticles; nanostructured lipid carriers; topical administration; lipid-based systems; n/a