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	<id>https://wiki.tiffa.net/w/index.php?action=history&amp;feed=atom&amp;title=Prosultiamine%2Fen</id>
	<title>Prosultiamine/en - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://wiki.tiffa.net/w/index.php?action=history&amp;feed=atom&amp;title=Prosultiamine%2Fen"/>
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	<updated>2026-04-19T23:47:30Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wiki.tiffa.net/w/index.php?title=Prosultiamine/en&amp;diff=133344&amp;oldid=prev</id>
		<title>FuzzyBot: Updating to match new version of source page</title>
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		<updated>2024-04-03T01:42:53Z</updated>

		<summary type="html">&lt;p&gt;Updating to match new version of source page&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;lt;languages /&amp;gt;&lt;br /&gt;
{{Short description|Chemical compound}}&lt;br /&gt;
{{Drugbox&lt;br /&gt;
| IUPAC_name = &amp;#039;&amp;#039;N&amp;#039;&amp;#039;-[(4-amino-2-methylpyrimidin-5-yl)methyl]-&amp;#039;&amp;#039;N&amp;#039;&amp;#039;-[(1&amp;#039;&amp;#039;E&amp;#039;&amp;#039;)-4-hydroxy-1-methyl-2-(propyldisulfanyl)but-1-en-1-yl]formamide&lt;br /&gt;
| image = Prosultiamine.png&lt;br /&gt;
| alt = Skeletal formula of prosultiamine&lt;br /&gt;
| width = 240&lt;br /&gt;
| image2 = Prosultiamine 3D ball.png&lt;br /&gt;
| alt2 = Ball-and-stick model of the prosultiamine molecule&lt;br /&gt;
| width2 = 260&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Clinical data--&amp;gt;&lt;br /&gt;
| tradename =  &lt;br /&gt;
| Drugs.com = {{drugs.com|international|prosultiamine}}&lt;br /&gt;
| pregnancy_category =  &lt;br /&gt;
| legal_status = Rx-only&lt;br /&gt;
| routes_of_administration = [[Mouth|Oral]]&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Pharmacokinetic data--&amp;gt;&lt;br /&gt;
| bioavailability =  &lt;br /&gt;
| metabolism =  &lt;br /&gt;
| elimination_half-life =  &lt;br /&gt;
| excretion =&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Identifiers--&amp;gt;&lt;br /&gt;
| CAS_number = 59-58-5&lt;br /&gt;
| ATC_prefix = None&lt;br /&gt;
| ATC_suffix =  &lt;br /&gt;
| PubChem = 5355019&lt;br /&gt;
| ChemSpiderID = 4511078&lt;br /&gt;
| UNII_Ref = {{fdacite|correct|FDA}}&lt;br /&gt;
| UNII = UI32MM3XE3&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--Chemical data--&amp;gt;&lt;br /&gt;
| C=15 | H=24 | N=4 | O=2 | S=2 &lt;br /&gt;
| smiles = O=CN(\C(=C(\SSCCC)CCO)C)Cc1cnc(nc1N)C&lt;br /&gt;
}}&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Prosultiamine&amp;#039;&amp;#039;&amp;#039; ([[International Nonproprietary Name|INN]]; also known as &amp;#039;&amp;#039;&amp;#039;thiamine propyl disulfide&amp;#039;&amp;#039;&amp;#039; or &amp;#039;&amp;#039;&amp;#039;TPD&amp;#039;&amp;#039;&amp;#039;; brand name &amp;#039;&amp;#039;&amp;#039;Jubedel&amp;#039;&amp;#039;&amp;#039;,) is a [[disulfide]] [[thiamine]] [[derivative (chemistry)|derivative]] discovered in garlic in [[Japan]] in the 1950s, and is similar to [[allithiamine]]. It was developed as a treatment for [[Thiamine#Deficiency|vitamin B&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; deficiency]]. It has improved [[lipid]] [[solubility]] relative to thiamine and is not rate-limited by dependency on intestinal [[membrane transport protein|transporter]]s for absorption, hence the reasoning for its development.&lt;br /&gt;
&lt;br /&gt;
==Research==&lt;br /&gt;
It has been studied as a potential treatment for infection with [[human T-lymphotropic virus]] (HTLV), since it has been shown to reduce viral load and symptoms.&lt;br /&gt;
&lt;br /&gt;
== See also ==&lt;br /&gt;
* [[Vitamin B1 analogue|Vitamin B&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; analogue]]&lt;br /&gt;
&lt;br /&gt;
{{Vitamins}}&lt;br /&gt;
&lt;br /&gt;
{{二次利用|date=2 March 2024}}&lt;br /&gt;
[[Category:Formamides]]&lt;br /&gt;
[[Category:Organic disulfides]]&lt;br /&gt;
[[Category:Aminopyrimidines]]&lt;br /&gt;
[[Category:Thiamine]]&lt;/div&gt;</summary>
		<author><name>FuzzyBot</name></author>
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