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<dcvalue element="contributor" qualifier="author">Lee,&#x20;Eun&#x20;Ha</dcvalue>
<dcvalue element="contributor" qualifier="author">Popov,&#x20;S.&#x20;A.</dcvalue>
<dcvalue element="contributor" qualifier="author">Lee,&#x20;Joo&#x20;Young</dcvalue>
<dcvalue element="contributor" qualifier="author">Shpatov,&#x20;A.&#x20;V.</dcvalue>
<dcvalue element="contributor" qualifier="author">Kukina,&#x20;T.&#x20;P.</dcvalue>
<dcvalue element="contributor" qualifier="author">Kang,&#x20;Suk&#x20;Woo</dcvalue>
<dcvalue element="contributor" qualifier="author">Pan,&#x20;Cheol&#x20;Ho</dcvalue>
<dcvalue element="contributor" qualifier="author">Um,&#x20;Byung&#x20;Hun</dcvalue>
<dcvalue element="contributor" qualifier="author">Jung,&#x20;Sang&#x20;Hoon</dcvalue>
<dcvalue element="date" qualifier="accessioned">2024-01-20T16:31:30Z</dcvalue>
<dcvalue element="date" qualifier="available">2024-01-20T16:31:30Z</dcvalue>
<dcvalue element="date" qualifier="created">2021-09-05</dcvalue>
<dcvalue element="date" qualifier="issued">2011-09</dcvalue>
<dcvalue element="identifier" qualifier="issn">1068-1620</dcvalue>
<dcvalue element="identifier" qualifier="uri">https:&#x2F;&#x2F;pubs.kist.re.kr&#x2F;handle&#x2F;201004&#x2F;130042</dcvalue>
<dcvalue element="description" qualifier="abstract">Aldose&#x20;reductase&#x20;(AR)&#x20;is&#x20;the&#x20;first&#x20;enzyme&#x20;in&#x20;the&#x20;polyol&#x20;pathway.&#x20;AR&#x20;has&#x20;been&#x20;reported&#x20;to&#x20;play&#x20;an&#x20;important&#x20;role&#x20;in&#x20;the&#x20;pathogenesis&#x20;of&#x20;diabetic&#x20;complications.&#x20;Ursolic&#x20;acid&#x20;and&#x20;fourteen&#x20;synthetic&#x20;derivatives&#x20;with&#x20;ursane&#x20;skeleton&#x20;were&#x20;tested&#x20;for&#x20;recombinant&#x20;human&#x20;aldose&#x20;reductase&#x20;(rhAR)&#x20;inhibitory&#x20;activity&#x20;for&#x20;development&#x20;of&#x20;diabetic&#x20;complications.&#x20;Among&#x20;them,&#x20;N-(3&#x20;beta-hydroxyurs-12-en-28-oyl)-4-aminobutyric&#x20;acid&#x20;(XV)&#x20;showed&#x20;most&#x20;potent&#x20;rhAR&#x20;inhibitory&#x20;activity&#x20;in&#x20;vitro.&#x20;Inhibition&#x20;mode&#x20;of&#x20;N-(3&#x20;beta-hydroxyurs-12-en-28-oyl)-4-aminobutyric&#x20;acid&#x20;(XV)&#x20;was&#x20;tested&#x20;uncompetitively&#x20;by&#x20;kinetic&#x20;analysis&#x20;using&#x20;the&#x20;Lineweaver-Burk&#x20;plots.&#x20;Ursolic&#x20;acid&#x20;derivative&#x20;N-(3&#x20;beta-hydroxyurs-12-en-28-oyl)-4-aminobutyric&#x20;acid&#x20;is&#x20;able&#x20;to&#x20;inhibit&#x20;rhAR&#x20;uncompetitively&#x20;and&#x20;could&#x20;be&#x20;offered&#x20;as&#x20;a&#x20;lead&#x20;compound&#x20;for&#x20;AR&#x20;inhibition.</dcvalue>
<dcvalue element="language" qualifier="none">English</dcvalue>
<dcvalue element="publisher" qualifier="none">MAIK&#x20;NAUKA&#x2F;INTERPERIODICA&#x2F;SPRINGER</dcvalue>
<dcvalue element="subject" qualifier="none">DIABETIC&#x20;COMPLICATIONS</dcvalue>
<dcvalue element="subject" qualifier="none">TRITERPENES</dcvalue>
<dcvalue element="subject" qualifier="none">SORBINIL</dcvalue>
<dcvalue element="title" qualifier="none">Inhibitory&#x20;effect&#x20;of&#x20;ursolic&#x20;acid&#x20;derivatives&#x20;on&#x20;recombinant&#x20;human&#x20;aldose&#x20;reductase</dcvalue>
<dcvalue element="type" qualifier="none">Article</dcvalue>
<dcvalue element="identifier" qualifier="doi">10.1134&#x2F;S1068162011050050</dcvalue>
<dcvalue element="description" qualifier="journalClass">1</dcvalue>
<dcvalue element="identifier" qualifier="bibliographicCitation">RUSSIAN&#x20;JOURNAL&#x20;OF&#x20;BIOORGANIC&#x20;CHEMISTRY,&#x20;v.37,&#x20;no.5,&#x20;pp.569&#x20;-&#x20;577</dcvalue>
<dcvalue element="citation" qualifier="title">RUSSIAN&#x20;JOURNAL&#x20;OF&#x20;BIOORGANIC&#x20;CHEMISTRY</dcvalue>
<dcvalue element="citation" qualifier="volume">37</dcvalue>
<dcvalue element="citation" qualifier="number">5</dcvalue>
<dcvalue element="citation" qualifier="startPage">569</dcvalue>
<dcvalue element="citation" qualifier="endPage">577</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scie</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scopus</dcvalue>
<dcvalue element="identifier" qualifier="wosid">000295533200007</dcvalue>
<dcvalue element="identifier" qualifier="scopusid">2-s2.0-80055000521</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Biochemistry&#x20;&amp;&#x20;Molecular&#x20;Biology</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Chemistry,&#x20;Organic</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Biochemistry&#x20;&amp;&#x20;Molecular&#x20;Biology</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Chemistry</dcvalue>
<dcvalue element="type" qualifier="docType">Article</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">DIABETIC&#x20;COMPLICATIONS</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">TRITERPENES</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">SORBINIL</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">aldose&#x20;reductase</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">N-(3&#x20;beta-hydroxyurs-12-en-28-oyl)-4-aminobutyric&#x20;acid</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">ursolic&#x20;acid&#x20;derivatives</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">diabetic&#x20;complications</dcvalue>
</dublin_core>
