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	<id>https://wiki.tiffa.net/w/index.php?action=history&amp;feed=atom&amp;title=Translations%3AFlavin_mononucleotide%2F1%2Fja</id>
	<title>Translations:Flavin mononucleotide/1/ja - 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=Translations%3AFlavin_mononucleotide%2F1%2Fja"/>
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	<updated>2026-05-12T08:18:47Z</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=Translations:Flavin_mononucleotide/1/ja&amp;diff=136760&amp;oldid=prev</id>
		<title>Fire: Created page with &quot;{{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 461100522 | ImageFile = Flavin mononucleotide v2.svg | ImageSize = 180 | ImageAlt = フラビンモノヌクレオチドの骨格式 | ImageFile1 = Flavin mononucleotide 3D ball.png | ImageSize1 = 180 | ImageAlt1 = フラビンモノヌクレオチド分子のボール＆スティックモデル | IUPACName = 1-Deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[&#039;&#039;g&#039;&#039;]pteridin-10(2&#039;&#039;H&#039;&#039;)-yl)-&lt;s...&quot;</title>
		<link rel="alternate" type="text/html" href="https://wiki.tiffa.net/w/index.php?title=Translations:Flavin_mononucleotide/1/ja&amp;diff=136760&amp;oldid=prev"/>
		<updated>2024-04-10T06:22:36Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;{{chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 461100522 | ImageFile = Flavin mononucleotide v2.svg | ImageSize = 180 | ImageAlt = フラビンモノヌクレオチドの骨格式 | ImageFile1 = Flavin mononucleotide 3D ball.png | ImageSize1 = 180 | ImageAlt1 = フラビンモノヌクレオチド分子のボール＆スティックモデル | IUPACName = 1-Deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[&amp;#039;&amp;#039;g&amp;#039;&amp;#039;]pteridin-10(2&amp;#039;&amp;#039;H&amp;#039;&amp;#039;)-yl)-&amp;lt;s...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{chembox&lt;br /&gt;
| Verifiedfields = changed&lt;br /&gt;
| Watchedfields = changed&lt;br /&gt;
| verifiedrevid = 461100522&lt;br /&gt;
| ImageFile = Flavin mononucleotide v2.svg&lt;br /&gt;
| ImageSize = 180&lt;br /&gt;
| ImageAlt = フラビンモノヌクレオチドの骨格式&lt;br /&gt;
| ImageFile1 = Flavin mononucleotide 3D ball.png&lt;br /&gt;
| ImageSize1 = 180&lt;br /&gt;
| ImageAlt1 = フラビンモノヌクレオチド分子のボール＆スティックモデル&lt;br /&gt;
| IUPACName = 1-Deoxy-1-(7,8-dimethyl-2,4-dioxo-3,4-dihydrobenzo[&amp;#039;&amp;#039;g&amp;#039;&amp;#039;]pteridin-10(2&amp;#039;&amp;#039;H&amp;#039;&amp;#039;)-yl)-&amp;lt;small&amp;gt;D&amp;lt;/small&amp;gt;-ribitol 5-(dihydrogen phosphate)&lt;br /&gt;
| SystematicName = (2&amp;#039;&amp;#039;R&amp;#039;&amp;#039;,3&amp;#039;&amp;#039;S&amp;#039;&amp;#039;,4&amp;#039;&amp;#039;S&amp;#039;&amp;#039;)-5-(7,8-Dimethyl-2,4-dioxo-3,4-dihydrobenzo[&amp;#039;&amp;#039;g&amp;#039;&amp;#039;]pteridin-10(2&amp;#039;&amp;#039;H&amp;#039;&amp;#039;)-yl)-2,3,4-trihydroxypentyl dihydrogen phosphate&lt;br /&gt;
| OtherNames = {{Unbulleted list|FMN}}&lt;br /&gt;
|Section1={{Chembox Identifiers&lt;br /&gt;
| IUPHAR_ligand = 5185&lt;br /&gt;
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}&lt;br /&gt;
| ChemSpiderID = 559060&lt;br /&gt;
| UNII_Ref = {{fdacite|correct|FDA}}&lt;br /&gt;
| UNII = 7N464URE7E&lt;br /&gt;
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}&lt;br /&gt;
| StdInChI = 1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1&lt;br /&gt;
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}&lt;br /&gt;
| StdInChIKey = FVTCRASFADXXNN-SCRDCRAPSA-N&lt;br /&gt;
| CASNo_Ref = {{cascite|correct|CAS}}&lt;br /&gt;
| CASNo = 146-17-8&lt;br /&gt;
| CASNo2_Ref = {{cascite|correct|CAS}}&lt;br /&gt;
| CASNo2 = 130-40-5&lt;br /&gt;
| CASNo2_Comment = (sodium salt)&lt;br /&gt;
| ChEMBL_Ref = {{ebicite|changed|EBI}}&lt;br /&gt;
| ChEMBL = 1201794&lt;br /&gt;
| PubChem = 643976&lt;br /&gt;
| ChEBI_Ref = {{ebicite|correct|EBI}}&lt;br /&gt;
| ChEBI = 17621&lt;br /&gt;
| SMILES = Cc1cc2c(cc1C)n(c-3nc(=O)[nH]c(=O)c3n2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O&lt;br /&gt;
| MeSHName = Flavin+mononucleotide&lt;br /&gt;
  }}&lt;br /&gt;
|Section2={{Chembox Properties&lt;br /&gt;
| Formula = C&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;21&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;9&amp;lt;/sub&amp;gt;P&lt;br /&gt;
| MolarMass = 456.344 g/mol&lt;br /&gt;
| Appearance = &lt;br /&gt;
| Density = &lt;br /&gt;
| MeltingPt = 195 °C&lt;br /&gt;
| BoilingPt = &lt;br /&gt;
  }}&lt;br /&gt;
|Section3={{Chembox Hazards&lt;br /&gt;
| MainHazards = &lt;br /&gt;
| FlashPt = &lt;br /&gt;
| AutoignitionPt = &lt;br /&gt;
  }}&lt;br /&gt;
}}&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;フラビンモノヌクレオチド&amp;#039;&amp;#039;&amp;#039;（&amp;#039;&amp;#039;&amp;#039;FMN&amp;#039;&amp;#039;&amp;#039;）、または&amp;#039;&amp;#039;&amp;#039;リボフラビン-5′-リン酸&amp;#039;&amp;#039;&amp;#039;は、酵素[[riboflavin kinase/ja|リボフラビンキナーゼ]]によって[[riboflavin/ja|リボフラビン]]（ビタミンB&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;）から生成される[[biomolecule/ja|生体分子]]であり、[[NADH dehydrogenase/ja|NADHデヒドロゲナーゼ]]を含む様々な[[oxidoreductase/ja|酸化還元酵素]]の[[prosthetic group/ja|補欠基]]として機能する。触媒サイクルの間、酸化型（FMN）、セミキノン型（FMNH&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;）、還元型（FMNH&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;）の可逆的な相互変換が様々な酸化還元酵素で起こる。FMNは[[Nicotinamide adenine dinucleotide/ja|NAD]]よりも強い酸化剤であり、1電子移動と2電子移動の両方に関与できるので特に有用である。青色光受容体としての役割において、（酸化）FMNはE/Z異性化ではなく、シグナル伝達状態として「従来の」光受容体より際立っている。&lt;/div&gt;</summary>
		<author><name>Fire</name></author>
	</entry>
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