Cytotoxicity and Anti-inflammatory Properties of Apigenin-Derived Isolaxifolin

dc.contributor.authorChen, Yongsheng
dc.contributor.authorChen, Wan-Na
dc.contributor.authorHu, Nan
dc.contributor.authorBanwell, Martin
dc.contributor.authorMa, Chenxi
dc.contributor.authorLan, Ping
dc.contributor.authorGardiner, Michael
dc.date.accessioned2020-09-21T02:51:38Z
dc.date.issued2019
dc.date.updated2020-06-23T00:56:25Z
dc.description.abstractThe rare flavonoid isolaxifolin, a potent insecticide, has been touted as a potential grain-protecting agent. In order to assess any impact of this natural product on human health and to explore its various other biological properties, we have established a semisynthesis from the simpler but structurally related and more abundant natural product apigenin. The five-step reaction sequence has provided, for the first time, sufficient material for an indepth evaluation of the cytotoxic properties of the title natural product. The impact of isolaxifolin on certain pro-inflammatory cytokines in murine macrophage RAW 264.7 cells has also been examined. Such studies have revealed that isolaxifolin displays no toxic effects toward normal cells while displaying greater cytotoxicities against certain cancer cell lines than its synthetic precursor apigenin. Furthermore, unlike apigenin, isolaxifolin only reduced NO, TNF-α, and IL-6 secretions in LPS-induced RAW 264.7 cells in a rather modest and dose-independent manner.en_AU
dc.description.sponsorshipThe authors thank the Chinese National Natural Science Foundation (grant 31700670, 21801094), the Program for Guangdong YangFan Introducing Innovative and Entrepreneurial Teams (grant 2016YT03H132), and the Department of Science and Technology of Guangdong Province under grant 2016A010105010 for financial support. Some of the X-ray crystallographic studies reported herein were undertaken on the MX1 beamline at the Australian Synchrotron (Melbourne) and part of Australia’s Nuclear Science and Technology Organization (ANSTO).en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0163-3864en_AU
dc.identifier.urihttp://hdl.handle.net/1885/210958
dc.language.isoen_AUen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.rights© 2019 American Chemical Society and American Society of Pharmacognosyen_AU
dc.sourceJournal of Natural Productsen_AU
dc.titleCytotoxicity and Anti-inflammatory Properties of Apigenin-Derived Isolaxifolinen_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue9en_AU
local.bibliographicCitation.lastpage2459en_AU
local.bibliographicCitation.startpage2451en_AU
local.contributor.affiliationChen, Yongsheng, Jinan Universityen_AU
local.contributor.affiliationChen, Wan-Na, Jinan Universityen_AU
local.contributor.affiliationHu, Nan, Jinan Universityen_AU
local.contributor.affiliationBanwell, Martin, College of Science, ANUen_AU
local.contributor.affiliationMa, Chenxi, College of Science, ANUen_AU
local.contributor.affiliationLan, Ping, Jinan Universityen_AU
local.contributor.affiliationGardiner, Michael, College of Science, ANUen_AU
local.contributor.authoruidBanwell, Martin, u9500594en_AU
local.contributor.authoruidMa, Chenxi, u5013394en_AU
local.contributor.authoruidGardiner, Michael, u1072089en_AU
local.description.embargo2037-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor030503 - Organic Chemical Synthesisen_AU
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciencesen_AU
local.identifier.ariespublicationu5786633xPUB1063en_AU
local.identifier.citationvolume82en_AU
local.identifier.doi10.1021/acs.jnatprod.9b00113en_AU
local.identifier.scopusID2-s2.0-85072575103
local.publisher.urlhttp://pubs.acs.org/page/jnprdf/en_AU
local.type.statusPublished Versionen_AU

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