Isolation and Structure Elucidation of Bioactive Compounds (Dedicated to the memory of the late Professor Charles D. Hufford)

Muhammad Ilias, Charles Cantrell (Herausgeber)

Buch | Softcover

276 Seiten

2019
MDPI (Verlag)
978-3-03897-780-3 (ISBN)

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We are very pleased to introduce the Book Version of our Special Issue in Molecules dedicated to the memory of the late Professor Dr. Charles D. Hufford. The issue has been a huge success, with 22 full-length peer-reviewed papers and a tribute by Professor Alice M.Clark. Authors, reviewers, and collaborators from many countries across the worldhave contributed to this endeavour, and we are truly grateful to all. This Special Issue isrepresentative of the broad impact that “Charlie” had on the field of bioactive naturalproducts. This Special Issue comprises papers from Professor Hufford’s former students,colleagues, and collaborators throughout the world who have utilized a wide array ofstate-of-the-art techniques to examine diverse natural sources to isolate and identify avariety of natural products with a wide spectrum of biological activities, including somenew microbial transformations and insights into bioactive molecules. Many new bioactive compounds are described and reported here for the first time. Bioactivities reportedinclude cytotoxicity, antimicrobial activity, anti-inflammatory activity, antileishmanialactivity, antitrypanosomal activity, antimalarial activity, analgesic activity, and beneficialliver activities, just to name a few. This Special Issue will undoubtedly have a lasting impact on the field of bioactive natural products, as exemplified by the career of Dr. Hufford.Lastly, without the timely and outstanding contributions from all of you, this Special Issue would not have been possible. We thank you all very much for your contributions and your time devoted to this Special Issue in memory of a special person. Finally, we express ourgratitude and thanks to the journal Molecules and their excellent team of expert reviewers for giving us the support and opportunity to make this Special Issue a huge success!

Erscheinungsdatum	20.04.2019
Verlagsort	Basel
Sprache	englisch
Maße	170 x 244 mm
Themenwelt	Medizin / Pharmazie ► Pharmazie
Themenwelt	Naturwissenschaften ► Chemie ► Allgemeines / Lexika
Schlagworte	13(S)-hydroxyatisenoic acid derivative • acacetin • acacetin 7-methyl ether • acylphloroglucinol • aldose reductase inhibitor • Alkaloids • amphotericin B • Analgesic • antibacterial • anti-inflammatory • anti-leishmanial activity • antimalarial activity • Antimicrobial Resistance • Antioxidant activity • antipyretic • antitrypanosomal activity • Aromatic compounds • Arthrinium sp. • augustine N-oxide • Baccharis • Biological Activities • buphanisine N-oxide • C-26-oxidation • C-27-oxidation • Cardiomyogenesis • carotenoids • channel catfish • chromone • Cochlospermaceae • Cochlospermum vitifolium • columnaris disease • Coumarinolignans • Crinum amabile • cryptococcosis • Cryptococcus neoformans • Cunninghamella echinulata • cytochalasins • cytotoxic activity • Cytotoxicity • dietary supplement • Diterpene glycosides • diterpenes • DNA barcoding • (E)-8(17),12-labdadiene-15,16-dial • Endophytic Fungi • Factor VII • Factor X • Flavobacterium columnare • flavonoids • flavonoids glycosides • fluconazole • fusidic acid • gastro-resistant • GC/MS • HepG2 • herbal medicine • hop prenylflavanone • HPLC • HPLC-ESI-IT-MS/MS • IL-8 • inflammation • iNOS • insecticidal activity • isolation and elucidation • iso-stevioside X-ray structure • isoxanthohumol • Jatropha pelargoniifolia • jenipapo • leishmania donovani • Lignans • Litsea cubeba • liver activity • Malaria • maleimides • methicillin resistant Staphylococcus aureus (MRSA) • microbial transformation • Microparticles • Microscopy • Mitracarpus scaber Zucc. • Molecular Docking • molecular dynamics • monoamine oxidase-A • monoamine oxidase-B • Morus alba L. • MS/MS • multi-drug resistant (MDR) • muscadine • N/A • Natural Products • Nemania • Neurological disorder • neuroprotective agent • NF- B • Obesity • Pancreatic cancer • pentalogin • phlorogluciniol • phytotoxicity • plant pathogenic and endophytic fungi • Polyketide • prosopilosidine • Prosopis glandulosa • pyranoanthocyanin • rebaudioside A isomers • Resveratrol • Rubiaceae • SAR • Sesterterpene • Sterols • Stevia rebaudiana • stilbenes • Terpenes • thrombosis • Torreya taxifolia • Turnera diffusa • Vasculogenesis • Xylariaceae • zerumbol • Zingiber monatnum
ISBN-10	3-03897-780-2 / 3038977802
ISBN-13	978-3-03897-780-3 / 9783038977803
Zustand	Neuware