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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Lysergic_acid</id>
	<title>Lysergic acid - Revision history</title>
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	<updated>2026-04-27T01:53:06Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Lysergic_acid&amp;diff=6310175&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Lysergic_acid&amp;diff=6310175&amp;oldid=prev"/>
		<updated>2025-02-18T01:03:05Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 01:03, 18 February 2025&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l24&quot;&gt;Line 24:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 24:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Alkaloids]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Alkaloids]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Psychoactive drugs]]&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;[[Category:Psychoactive drugs]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;gallery&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:Lysergic_acid_chemical_structure.svg|Chemical structure of Lysergic acid&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-deleted&quot;&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;File:Lysergic_acid_isomers.png|Isomers of Lysergic acid&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
	<entry>
		<id>https://wikimd.org/index.php?title=Lysergic_acid&amp;diff=5356769&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Lysergic_acid&amp;diff=5356769&amp;oldid=prev"/>
		<updated>2024-03-04T02:57:09Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Lysergic acid&amp;#039;&amp;#039;&amp;#039; is an organic compound that forms the core structure of many ergoline alkaloids, which are found in a variety of organisms, including fungi, plants, and animals. It is best known as the precursor to [[LSD]] (lysergic acid diethylamide), a powerful psychedelic drug.&lt;br /&gt;
&lt;br /&gt;
==Chemistry==&lt;br /&gt;
Lysergic acid is a complex molecule with a unique structure. It is a carboxylic acid that contains a bicyclic structure, which is composed of a hexahydroindole fused to a bicyclic quinoline group (lysergic acid is hence a polycyclic amine). This core structure is common to all lysergic acid derivatives, including LSD.&lt;br /&gt;
&lt;br /&gt;
==Biosynthesis==&lt;br /&gt;
In nature, lysergic acid is produced by the fungus &amp;#039;&amp;#039;[[Claviceps purpurea]]&amp;#039;&amp;#039;, which infects rye and other grains. The fungus synthesizes lysergic acid as part of its secondary metabolism, using the amino acid tryptophan as a precursor. The biosynthesis process involves several enzymatic steps, including decarboxylation, condensation, and oxidation.&lt;br /&gt;
&lt;br /&gt;
==Uses==&lt;br /&gt;
Lysergic acid is primarily known for its role in the synthesis of LSD, but it also serves as a precursor for other ergoline alkaloids. These compounds have a wide range of pharmacological effects and have been used in the treatment of various medical conditions, such as migraines and Parkinson&amp;#039;s disease.&lt;br /&gt;
&lt;br /&gt;
==Safety==&lt;br /&gt;
While lysergic acid itself is not a controlled substance, many of its derivatives are. These include LSD, which is a Schedule I controlled substance in the United States. Exposure to lysergic acid can cause skin and eye irritation, and ingestion can lead to hallucinations and other psychological effects.&lt;br /&gt;
&lt;br /&gt;
==See also==&lt;br /&gt;
* [[Ergoline]]&lt;br /&gt;
* [[LSD]]&lt;br /&gt;
* [[Claviceps purpurea]]&lt;br /&gt;
&lt;br /&gt;
{{Chem-stub}}&lt;br /&gt;
&lt;br /&gt;
[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Carboxylic acids]]&lt;br /&gt;
[[Category:Alkaloids]]&lt;br /&gt;
[[Category:Psychoactive drugs]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
	</entry>
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