<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Natural Products &#8211; ChemiMart</title>
	<atom:link href="https://www.chemimart.de/product-category/natural-products/feed/" rel="self" type="application/rss+xml" />
	<link>https://www.chemimart.de</link>
	<description>Professional expertise in chemical research and preparation of complex organic compounds from Berlin-Adlershof. We do chemistry for you!</description>
	<lastBuildDate>Thu, 08 Dec 2022 15:38:47 +0000</lastBuildDate>
	<language>en-GB</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=6.8.3</generator>

<image>
	<url>https://www.chemimart.de/wp-content/uploads/2020/11/cropped-chemimart-favicon-32x32.png</url>
	<title>Natural Products &#8211; ChemiMart</title>
	<link>https://www.chemimart.de</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>DL-indole Lactic Acid</title>
		<link>https://www.chemimart.de/product/dl-indole-lactic-acid/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:14:32 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=738</guid>

					<description><![CDATA[This alpha-hydroxy acid can be used as a Tryptophan analogue, for example in the preparation of depsipeptides. Ref.: &#160; 1) VERFAHREN ZUR HERSTELLUNG VON INDOLYLMILCHSAEURE TENUD LEANDER DR Patent #: DE2440419A1 DOI: N/A]]></description>
										<content:encoded><![CDATA[<p>This alpha-hydroxy acid can be used as a Tryptophan analogue, for example in the preparation of depsipeptides.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1) VERFAHREN ZUR HERSTELLUNG VON INDOLYLMILCHSAEURE</p>
<p>TENUD LEANDER DR</p>
<p>Patent #: DE2440419A1<br />
DOI: N/A</p>
]]></content:encoded>
					
		
		
			</item>
		<item>
		<title>(±)-8-Prenylnaringenin</title>
		<link>https://www.chemimart.de/product/%c2%b1-8-prenylnaringenin/</link>
		
		<dc:creator><![CDATA[mzaug]]></dc:creator>
		<pubDate>Wed, 09 Dec 2020 15:12:04 +0000</pubDate>
				<guid isPermaLink="false">https://www.chemimart.de/?post_type=product&#038;p=732</guid>

					<description><![CDATA[8-Prenylnaringenin (8-PN; also known as flavaprenin, (S)-8-dimethylallylnaringenin, hopein, or sophoraflavanone B) is a prenylflavonoid phytoestrogen. It is reported to be the most estrogenic phytoestrogen known. Ref.: &#160; 1) Molecular docking and panicolytic effect of 8-​prenylnaringenin in the elevated T-​maze Chemical &#38; Pharmaceutical Bulletin, 2014, 62(12), 1231-1237 Bagatin, Mariane Cristovao; Tozatti, Camila Santos Suniga; Abiko, Layara Akemi; [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>8-Prenylnaringenin (8-PN; also known as flavaprenin, (S)-8-dimethylallylnaringenin, hopein, or sophoraflavanone B) is a prenylflavonoid phytoestrogen. It is reported to be the most estrogenic phytoestrogen known.</p>
<p><em>Ref.:</em></p>
<p>&nbsp;</p>
<p>1) Molecular docking and panicolytic effect of 8-​prenylnaringenin in the elevated T-​maze</p>
<p><em>Chemical &amp; Pharmaceutical Bulletin</em>, <strong>2014,</strong> <em>62</em>(12), 1231-1237<br />
Bagatin, Mariane Cristovao; Tozatti, Camila Santos Suniga; Abiko, Layara Akemi; Yamazaki, et al.</p>
<p>DOI: 10.1248/cpb.c14-00569</p>
]]></content:encoded>
					
		
		
			</item>
	</channel>
</rss>
