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	<id>https://bsd.neuroinf.jp/w/index.php?action=history&amp;feed=atom&amp;title=%CE%92-Zearalenol</id>
	<title>Β-Zearalenol - 版の履歴</title>
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	<updated>2026-04-12T11:39:23Z</updated>
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		<title>WikiSysop: 1版 をインポートしました</title>
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		<updated>2025-03-18T10:35:26Z</updated>

		<summary type="html">&lt;p&gt;1版 をインポートしました&lt;/p&gt;
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		<author><name>WikiSysop</name></author>
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		<id>https://bsd.neuroinf.jp/w/index.php?title=%CE%92-Zearalenol&amp;diff=49975&amp;oldid=prev</id>
		<title>2023年9月15日 (金) 21:20にbsd&gt;Hyphenation Expertによる</title>
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		<updated>2023-09-15T21:20:24Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新規ページ&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{Short description|Chemical compound}}&lt;br /&gt;
{{lowercase title}}&lt;br /&gt;
{{Drugbox&lt;br /&gt;
| Verifiedfields = &lt;br /&gt;
| Watchedfields = &lt;br /&gt;
| verifiedrevid = &lt;br /&gt;
| drug_name = β-Zearalenol&lt;br /&gt;
| IUPAC_name = (2&amp;#039;&amp;#039;E&amp;#039;&amp;#039;,7&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,11&amp;#039;&amp;#039;S&amp;#039;&amp;#039;)-7,15,17-trihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(18),2,14,16-tetraen-13-one&lt;br /&gt;
| image = Beta Zearalenol.svg&lt;br /&gt;
| width =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Clinical data--&amp;gt;&lt;br /&gt;
| tradename = &lt;br /&gt;
| pregnancy_AU = &amp;lt;!-- A / B1 / B2 / B3 / C / D / X --&amp;gt;&lt;br /&gt;
| pregnancy_US = &amp;lt;!-- A / B            / C / D / X --&amp;gt;&lt;br /&gt;
| pregnancy_category = &lt;br /&gt;
| legal_AU = &amp;lt;!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --&amp;gt;&lt;br /&gt;
| legal_CA = &lt;br /&gt;
| legal_UK = &lt;br /&gt;
| legal_US = &lt;br /&gt;
| legal_status = &lt;br /&gt;
| routes_of_administration =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Pharmacokinetic data--&amp;gt;&lt;br /&gt;
| bioavailability = &lt;br /&gt;
| protein_bound = &lt;br /&gt;
| metabolism = &lt;br /&gt;
| elimination_half-life = &lt;br /&gt;
| excretion =&lt;br /&gt;
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&amp;lt;!-- Identifiers --&amp;gt;&lt;br /&gt;
| CAS_number_Ref = &lt;br /&gt;
| CAS_number = 71030-11-0&lt;br /&gt;
| CAS_supplemental = &lt;br /&gt;
| ATC_prefix = &lt;br /&gt;
| ATC_suffix = &lt;br /&gt;
| ATC_supplemental = &lt;br /&gt;
| PubChem = 6437352&lt;br /&gt;
| IUPHAR_ligand = &lt;br /&gt;
| DrugBank_Ref = &lt;br /&gt;
| DrugBank = &lt;br /&gt;
| ChemSpiderID_Ref = &lt;br /&gt;
| ChemSpiderID = 5908979&lt;br /&gt;
| UNII = 35E809PP7O&lt;br /&gt;
| KEGG = C14751&lt;br /&gt;
| ChEBI = 35072&lt;br /&gt;
| ChEMBL =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Chemical data--&amp;gt;&lt;br /&gt;
| C=18 | H=24 | O=5&lt;br /&gt;
| SMILES = C[C@H]1CCC[C@H](CCC/C=C/C2=CC(=CC(=C2C(=O)O1)O)O)O&lt;br /&gt;
| StdInChI_Ref = &lt;br /&gt;
| StdInChI = 1S/C18H24O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h3,7,10-12,14,19-21H,2,4-6,8-9H2,1H3/b7-3+/t12-,14-/m0/s1&lt;br /&gt;
| StdInChIKey_Ref = &lt;br /&gt;
| StdInChIKey = FPQFYIAXQDXNOR-PMRAARRBSA-N&lt;br /&gt;
| synonyms = beta-Zearalenol; beta-&amp;#039;&amp;#039;trans&amp;#039;&amp;#039;-Zearalenol&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;β-Zearalenol&amp;#039;&amp;#039;&amp;#039; is a [[nonsteroidal]] [[estrogen]] of the [[resorcylic acid lactone]] group related to [[mycoestrogen]]s found in &amp;#039;&amp;#039;[[Fusarium|Fusarium spp]]&amp;#039;&amp;#039;.&amp;lt;ref name=&amp;quot;Chelkowski2014&amp;quot;&amp;gt;{{cite book | vauthors = Bottalico A, Logrieco A, Visconti A | chapter = Fusarium species and their mycotoxins in infected cereals in the field and in stored grains | title = Fusarium: Mycotoxins, Taxonomy, Pathogenicity | date = January 1989 | pages = 85–119 | veditors = Chelkowski J | chapter-url=https://books.google.com/books?id=_1KeBQAAQBAJ&amp;amp;pg=PA85 |publisher=Elsevier Science |isbn=978-1-4832-9785-9 }}&amp;lt;/ref&amp;gt; It is the β [[epimer]] of [[α-zearalenol]] and along with α-zearalenol is a major [[metabolite]] of [[zearalenone]] formed mainly in the [[liver]] but also to a lesser extent in the [[intestine]]s during [[first-pass metabolism]].&amp;lt;ref name=&amp;quot;MaganOlsen2004&amp;quot;&amp;gt;{{cite book | vauthors = Alldrick AJ, Hajšelová M | chapter = Zearalenone | title = Mycotoxins in Food: Detection and Control | date = January 2004 | pages = 353–366 | publisher =  Woodhead Publishing | veditors = Magan N, Olsen M | chapter-url=https://books.google.com/books?id=CZ3iEhPeejoC&amp;amp;pg=PA356 |isbn=978-1-85573-733-4 }}&amp;lt;/ref&amp;gt;&amp;lt;ref name=&amp;quot;Eriksen1998&amp;quot;&amp;gt;{{cite book | chapter = Zearalenone | vauthors = Eriksen GS, Alexander J  |title=Fusarium Toxins in Cereals: A Risk Assessment| chapter-url=https://books.google.com/books?id=jU5Wx8LkZHUC&amp;amp;pg=PA61|year=1998|publisher=Nordic Council of Ministers|isbn=978-92-893-0149-7|pages=61–}}&amp;lt;/ref&amp;gt; A relatively high proportion of α-zearalenol is formed from zearalenone compared to β-zearalenol in humans.&amp;lt;ref name=&amp;quot;Eriksen1998&amp;quot; /&amp;gt; β-Zearalenol is about the same or slightly less potent as an estrogen relative to zearalenone.&amp;lt;ref name=&amp;quot;Chelkowski2014&amp;quot; /&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
* [[Taleranol]] (β-zearalanol)&lt;br /&gt;
* [[Zeranol]] (α-zearalanol)&lt;br /&gt;
* [[Zearalanone]]&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
{{reflist|30em}}&lt;br /&gt;
&lt;br /&gt;
{{Estrogen receptor modulators}}&lt;br /&gt;
&lt;br /&gt;
{{DEFAULTSORT:Zearalenol, alpha-}}&lt;br /&gt;
[[Category:Lactones]]&lt;br /&gt;
[[Category:Mycoestrogens]]&lt;br /&gt;
[[Category:Mycotoxins]]&lt;br /&gt;
[[Category:Resorcinols]]&lt;/div&gt;</summary>
		<author><name>bsd&gt;Hyphenation Expert</name></author>
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