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	<id>https://arolstar52-zhtest.hf.space/index.php?action=history&amp;feed=atom&amp;title=Montrifoline</id>
	<title>Montrifoline - 版本历史</title>
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	<updated>2026-07-21T00:16:14Z</updated>
	<subtitle>本wiki上该页面的版本历史</subtitle>
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	<entry>
		<id>https://arolstar52-zhtest.hf.space/index.php?title=Montrifoline&amp;diff=4483311&amp;oldid=prev</id>
		<title>2024年10月4日 (五) 02:24 imported&gt;Innerstream</title>
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		<updated>2024-10-04T02:24:58Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新页面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{NotChineseTitle|time=2024-08-02T12:27:33+00:00}}&lt;br /&gt;
{{Chembox&lt;br /&gt;
| Name = &lt;br /&gt;
| NameEn = &lt;br /&gt;
| ImageFile = Montrifoline.svg&lt;br /&gt;
|  ImageSize = &lt;br /&gt;
|  ImageAlt = &lt;br /&gt;
| IUPACName = &lt;br /&gt;
| IUPACNameZh = &lt;br /&gt;
| OtherNames = &lt;br /&gt;
| Section1 = {{Chembox Identifiers&lt;br /&gt;
|   CASNo = 77145-74-5&lt;br /&gt;
|   CASNo_Ref = {{cascite|correct|CAS}}&lt;br /&gt;
|   PubChem = &lt;br /&gt;
|   SMILES =  }}&lt;br /&gt;
| Section2 = {{Chembox Properties&lt;br /&gt;
| C=18 | H=21 | N=1 | O=6&lt;br /&gt;
|   Appearance = 无色针状晶体&amp;lt;ref name=Johnson&amp;gt;Johnson Foyere Ayafor; Joseph I. Okogun. Nkolbisine, a New Furoquinoline Alkaloid, and 7-Deacetylazadirone From Teclea verdoorniana. J. Nat. Prod. 1982, 45, 2, 182–185. {{doi|10.1021/np50020a012}}.&amp;lt;/ref&amp;gt;&lt;br /&gt;
|   Density = &lt;br /&gt;
|   MeltingPt = 189-190 °C&amp;lt;ref name=Johnson /&amp;gt;&lt;br /&gt;
|   BoilingPt = &lt;br /&gt;
|   Solubility =  }}&lt;br /&gt;
| Section3 = {{Chembox Hazards&lt;br /&gt;
|   MainHazards = &lt;br /&gt;
|   FlashPt = &lt;br /&gt;
|   Autoignition =  }}&lt;br /&gt;
}}&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Montrifoline&amp;#039;&amp;#039;&amp;#039;是一种有机化合物，化学式为[[C18H21NO6|C&amp;lt;sub&amp;gt;18&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;21&amp;lt;/sub&amp;gt;NO&amp;lt;sub&amp;gt;6&amp;lt;/sub&amp;gt;]]，其名称源自于植物&amp;#039;&amp;#039;Monnieria trifoliata&amp;#039;&amp;#039;。&amp;lt;ref name=Grundon /&amp;gt;它也存在于&amp;#039;&amp;#039;{{lwd|Q39840058}}&amp;#039;&amp;#039;和&amp;#039;&amp;#039;Teclea ouabanguiensis&amp;#039;&amp;#039;植物中。&amp;lt;ref name=Grundon&amp;gt;M. F. Grundon. Quinoline, Quinazoline, and Acridone Alkaloids, Nat. Prod. Rep., 1984,1, 195-200. {{doi|10.1039/NP9840100195}}.&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
它和[[乙酸酐]]在[[吡啶]]存在下反应，可以得到乙酰基montrifoline。&amp;lt;ref&amp;gt;Damien Lacroix; Soizic Prado; Dennis Kamoga; John Kasenene; Bernard Bodo. Absolute configuration of 2′(R)-acetylmontrifoline and 2′(R)-montrifoline, furoquinolines from the fruits of Teclea nobilis. Phytochemistry Letters, 2012. 5 (1): 22-25. {{doi|10.1016/j.phytol.2011.08.012}}.&amp;lt;/ref&amp;gt;&lt;br /&gt;
==参考文献==&lt;br /&gt;
{{reflist}}&lt;br /&gt;
&lt;br /&gt;
==延伸阅读==&lt;br /&gt;
* Jean Duplex Wansi; et al. Oxidative Burst Inhibitory and Cytotoxic Indoloquinazoline and Furoquinoline Alkaloids from Oricia suaveolens. J. Nat. Prod. 2008, 71, 11, 1942–1945. {{doi|10.1021/np800276f}}.&lt;br /&gt;
&lt;br /&gt;
[[Category:苯甲醚]]&lt;/div&gt;</summary>
		<author><name>imported&gt;Innerstream</name></author>
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