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dc.contributor.authorHoenke, Sophie-
dc.contributor.authorChristoph, Martin A.-
dc.contributor.authorFriedrich, Sander-
dc.contributor.authorHeise, Niels-
dc.contributor.authorBrandes, Benjamin-
dc.contributor.authorDeigner, Hans-Peter-
dc.contributor.authorAl-Harrasi, Ahmed-
dc.contributor.authorCsuk, René-
dc.date.accessioned2022-03-22T08:02:24Z-
dc.date.available2022-03-22T08:02:24Z-
dc.date.issued2021-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/80100-
dc.identifier.urihttp://dx.doi.org/10.25673/78146-
dc.description.abstractPentacyclic triterpenoids oleanolic acid, ursolic acid, betulinic acid, and platanic acid were acetylated and converted into several amides 9–31; the cytotoxicity of which has been determined in sulforhodamine B assays employing seral human tumor cell lines and nonmalignant fibroblasts. Thereby, a betulinic acid/trans-1,4-cyclohexyldiamine amide showed excellent cytotoxicity (for example, EC50 = 0.6 μM for HT29 colon adenocarcinoma cells).eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc547-
dc.titleThe presence of a cyclohexyldiamine moiety confers cytotoxicity to pentacyclic triterpenoidseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleMolecules-
local.bibliographicCitation.volume26-
local.bibliographicCitation.issue7-
local.bibliographicCitation.publishernameMDPI-
local.bibliographicCitation.publisherplaceBasel-
local.bibliographicCitation.doi10.3390/molecules26072102-
local.openaccesstrue-
local.accessrights.dnbfree-
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