About: Chapter 4 Bioactivity and Synthesis of Diarylheptanoids From Alpinia officinarum

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An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Chapter 4 Bioactivity and Synthesis of Diarylheptanoids From Alpinia officinarum
Creator	Sun, Yi Kurokawa, Masahiko Miura, Motofumi Motohashi, Shigeyasu Yasukawa, Ken
Source	Elsevier; PMC
abstract	Abstract Many diarylheptanoids were isolated from the galangal (rhizome of Alpinia officinarum). We are reported the antitumor-promoting, antiinflammatory, cytotoxic, antiinfluenza virus, and antiherpes simplex-1 virus activities of diarylheptanoids. These components in our dietary and herbal supplements are considered to be relatively nontoxic to human. In addition, we synthesized the new compounds. In this review, we discuss the antitumor-promoting, antiinflammatory, cytotoxic, antimicrobial, antiinfluenza, and antiherpes simplex-1 virus activities of diarylheptanoids isolated from galangal resulting from our own and other research groups' investigation.
has issue date	2016-12-31(xsd:dateTime)
bibo:doi	10.1016/b978-0-444-63601-0.00004-1
has license	els-covid
sha1sum (hex)	fb6c45a24be82c4acc6242c783664a8d2f5ff52a
schema:url	https://doi.org/10.1016/b978-0-444-63601-0.00004-1
resource representing a document's title	Chapter 4 Bioactivity and Synthesis of Diarylheptanoids From Alpinia officinarum
has PubMed Central identifier	PMC7152183
schema:publication	Studies in Natural Products Chemistry
resource representing a document's body	covid:fb6c45a24be82c4acc6242c783664a8d2f5ff52a#body_text
is schema:about of	named entity 'DIARYLHEPTANOIDS' named entity 'CHAPTER' named entity 'OUTLINE' named entity 'SYNTHESIS' named entity 'BIOACTIVITY' named entity 'ALPINIA OFFICINARUM' named entity 'Alpinia officinarum' named entity 'influenza virus' named entity 'oncogene' named entity 'diarylheptanoids' named entity 'tumor' named entity 'diarylheptanoids' named entity 'EPEC' named entity 'Wittig reaction' named entity 'neuroblastoma' named entity 'kidneys' named entity 'antitumor' named entity 'mRNAs' named entity 'polysome' named entity 'C-5' named entity 'antiviral activity' named entity 'hyperlipidemic' named entity 'orlistat' named entity 'rectum' named entity 'ketone' named entity 'aqueous' named entity 'vomiting' named entity 'inhibitory activity' named entity 'H1N1' named entity 'fecal incontinence' named entity 'antiviral' named entity 'Bioassay' named entity 'hydroxylation' named entity 'GPCRs' named entity 'antiinflammatory' named entity 'stomach cancer' named entity 'pancreatic lipase' named entity 'genus' named entity 'heptane' named entity 'chiral center' named entity 'curries' named entity 'mRNAs' named entity 'steroids' named entity 'malabsorption' named entity 'lead compound' named entity 'diarrhea' named entity 'alcohol' named entity 'diarylheptanoids' named entity 'prostate' named entity 'human diseases' named entity 'microarray analysis' named entity 'control group' named entity 'tom yum' named entity 'Zingiberaceae' named entity 'activating transcription factor 3' named entity 'abortifacient' named entity 'tyrosinase' named entity 'Swern' named entity 'RSV' named entity 'Antiviral' named entity 'ICR mice' named entity 'Malaysia' named entity 'Red-Al' named entity 'melanoma' named entity '3,5' named entity 'pyridine' named entity 'rhizomes' named entity 'absolute configuration' named entity 'ribonucleoprotein' named entity 'crude drugs' named entity 'dietary fat' named entity 'apoptosis' named entity 'methoxy group' named entity 'diarylheptanoids' named entity 'cell line' named entity 'Fig' named entity 'diarylheptanoids' named entity 'emesis' named entity 'antipyretic'

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