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	<title>DesignCaffeine &#187; patent</title>
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		<title>US Patent #6677343: Substituted Piperazine Compounds</title>
		<link>http://www.designcaffeine.com/2010/inventions/250/</link>
		<comments>http://www.designcaffeine.com/2010/inventions/250/#comments</comments>
		<pubDate>Thu, 21 Jan 2010 06:14:45 +0000</pubDate>
		<dc:creator>Greg Nudelman</dc:creator>
				<category><![CDATA[Inventions]]></category>
		<category><![CDATA[biotech]]></category>
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		<description><![CDATA[Novel compounds of the general formula: ##STR1## and pharmaceutically acceptable acid addition salts thereof, wherein the compounds are useful in therapy to protect skeletal muscles against damage resulting from trauma or to protect skeletal muscles subsequent to muscle or systemic diseases such as intermittent claudication, to treat shock conditions, to preserve donor tissue and organs [...]]]></description>
			<content:encoded><![CDATA[<p>Novel compounds of the general formula: ##STR1## and pharmaceutically acceptable acid addition salts thereof, wherein the compounds are useful in therapy to protect skeletal muscles against damage resulting from trauma or to protect skeletal muscles subsequent to muscle or systemic diseases such as intermittent claudication, to treat shock conditions, to preserve donor tissue and organs used in transplants, in the treatment of cardiovascular diseases including atrial and ventricular arrhythmias, Prinzmetal&#8217;s (variant) angina, stable angina, and exercise induced angina, congestive heart disease, and myocardial infarction.</p>
<p><a href="http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&amp;Sect2=HITOFF&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&amp;r=1&amp;f=G&amp;l=50&amp;co1=AND&amp;d=PTXT&amp;s1=6677343.PN.&amp;OS=PN/6677343&amp;RS=PN/6677343" target="new">Granted by the US Patent Office February 22, 2001 ⇒</a></p>
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		<title>US Patent #6180615: Propargyl Phenyl Ether A2A Receptor Agonists</title>
		<link>http://www.designcaffeine.com/2010/inventions/247/</link>
		<comments>http://www.designcaffeine.com/2010/inventions/247/#comments</comments>
		<pubDate>Thu, 21 Jan 2010 06:13:21 +0000</pubDate>
		<dc:creator>Greg Nudelman</dc:creator>
				<category><![CDATA[Inventions]]></category>
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		<description><![CDATA[2-adenosine propargyl phenyl ether compositions having the following formula: ##STR1## and methods for using the compositions as A.sub.2A receptor agonists to stimulate mammalian coronary vasodilatation for therapeutic purposes and for purposes of imaging the heart.
Granted by the US Patent Office June 22, 1999 ⇒
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			<content:encoded><![CDATA[<p>2-adenosine propargyl phenyl ether compositions having the following formula: ##STR1## and methods for using the compositions as A.sub.2A receptor agonists to stimulate mammalian coronary vasodilatation for therapeutic purposes and for purposes of imaging the heart.</p>
<p><a href="http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&amp;Sect2=HITOFF&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&amp;r=1&amp;f=G&amp;l=50&amp;co1=AND&amp;d=PTXT&amp;s1=6180615.PN.&amp;OS=PN/6180615&amp;RS=PN/6180615" target="new">Granted by the US Patent Office June 22, 1999 ⇒</a></p>
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		<title>US Patent #6677336: Substituted Piperazine Compounds</title>
		<link>http://www.designcaffeine.com/2010/inventions/245/</link>
		<comments>http://www.designcaffeine.com/2010/inventions/245/#comments</comments>
		<pubDate>Thu, 21 Jan 2010 06:11:40 +0000</pubDate>
		<dc:creator>Greg Nudelman</dc:creator>
				<category><![CDATA[Inventions]]></category>
		<category><![CDATA[biotech]]></category>
		<category><![CDATA[patent]]></category>

		<guid isPermaLink="false">http://www.designcaffeine.com/?p=245</guid>
		<description><![CDATA[Novel compounds of the general formula: ##STR1## and pharmaceutically acceptable acid addition salts thereof, wherein the compounds are useful in therapy to protect skeletal muscles against damage resulting from trauma or to protect skeletal muscles subsequent to muscle or systemic diseases such as intermittent claudication, to treat shock conditions, to preserve donor tissue and organs [...]]]></description>
			<content:encoded><![CDATA[<p>Novel compounds of the general formula: ##STR1## and pharmaceutically acceptable acid addition salts thereof, wherein the compounds are useful in therapy to protect skeletal muscles against damage resulting from trauma or to protect skeletal muscles subsequent to muscle or systemic diseases such as intermittent claudication, to treat shock conditions, to preserve donor tissue and organs used in transplants, in the treatment of cardiovascular diseases including atrial and ventricular arrhythmias, Prinzmetal&#8217;s (variant) angina, stable angina, and exercise induced angina, congestive heart disease, and myocardial infarction.</p>
<p><a href="http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO2&amp;Sect2=HITOFF&amp;p=1&amp;u=%2Fnetahtml%2FPTO%2Fsearch-bool.html&amp;r=1&amp;f=G&amp;l=50&amp;co1=AND&amp;d=PTXT&amp;s1=6677336.PN.&amp;OS=PN/6677336&amp;RS=PN/6677336" target="new">Granted by the US Patent Office February 22, 2001 ⇒</a></p>
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