Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/81342
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dc.contributor.authorBrandes, Benjamin-
dc.contributor.authorHalz, Jan H.-
dc.contributor.authorMerzweiler, Kurt-
dc.contributor.authorDeigner, Hans-Peter-
dc.contributor.authorCsuk, René-
dc.date.accessioned2022-04-05T06:39:36Z-
dc.date.available2022-04-05T06:39:36Z-
dc.date.issued2022-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/83297-
dc.identifier.urihttp://dx.doi.org/10.25673/81342-
dc.description.abstractAzelastine is among the most frequently used drugs; however, knowledge and solid data about its metabolites are scarcely found in literature. Thus, microsomal oxidation of azelastine is thought to produce the corresponding N-oxides, However, until now these products had never been produced in significant amounts. By oxidation of azelastine with H2O2, these N-oxides were now prepared in racemic form for the first time and were fully characterized. Their structure was additionally confirmed by a single crystal X-ray analysis. Both N-oxides were found to be non-cytotoxic in SRB assays.eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc540-
dc.titleSynthesis and structure of azelastine-N-oxideseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleJournal of molecular structure-
local.bibliographicCitation.volume1251-
local.bibliographicCitation.publishernameElsevier-
local.bibliographicCitation.publisherplaceNew York, NY [u.a.]-
local.bibliographicCitation.doi10.1016/j.molstruc.2021.132033-
local.openaccesstrue-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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