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Revision as of 14:04, 17 February 2012 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Saving copy of the {{chembox}} taken from revid 467614911 of page Amurensin_(flavonol) for the Chem/Drugbox validation project (updated: 'CASNo').  Latest revision as of 10:42, 21 October 2024 edit JWBE (talk | contribs)Extended confirmed users10,111 edits +Category:4-Hydroxyphenyl compounds; ±Category:PhenolsCategory:Hydroxyarenes using HotCat 
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{{ambox | text = This page contains a copy of the infobox ({{tl|chembox}}) taken from revid of page ] with values updated to verified values.}}
{{chembox {{chembox
| Verifiedfields = changed
| verifiedrevid = 423447203
| Watchedfields = changed
| Name = Amurensin
| verifiedrevid = 477367232
| ImageFile = Amurensin.svg
| ImageSize = 250px | Name = Amurensin
| ImageFile = Amurensin.svg
| IUPACName = 3,5-dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-oxychromen-4-one
| OtherNames = | ImageSize = 250px
| ImageFile2 = Amurensin ball-and-stick.png
| Section1= {{Chembox Identifiers
| IUPACName = 7-(β-<small>D</small>-Glucopyranosyloxy)-3,4′,5-trihydroxy-8-(3-hydroxy-3-methylbutyl)flavone
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| SystematicName = 3,5-Dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-{oxy}-4''H''-1-benzopyran-4-one
| ChemSpiderID = 4476774
| OtherNames =
| InChI = 1/C26H30O12/c1-26(2,35)8-7-13-15(36-25-22(34)20(32)18(30)16(10-27)37-25)9-14(29)17-19(31)21(33)23(38-24(13)17)11-3-5-12(28)6-4-11/h3-6,9,16,18,20,22,25,27-30,32-35H,7-8,10H2,1-2H3/t16-,18-,20-,22-,25-/m1/s1
|Section1={{Chembox Identifiers
| InChIKey = UNHHWEHQUUGKEE-BGCJFSMVBS

| SMILES1 = O=C3c4c(O)cc(O1O((O)(O)1O)CO)c(c4O/C(c2ccc(O)cc2)=C3/O)CCC(O)(C)C
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 20120043
| StdInChI = 1S/C26H30O12/c1-26(2,35)8-7-13-15(36-25-22(34)20(32)18(30)16(10-27)37-25)9-14(29)17-19(31)21(33)23(38-24(13)17)11-3-5-12(28)6-4-11/h3-6,9,16,18,20,22,25,27-30,32-35H,7-8,10H2,1-2H3/t16-,18-,20-,22-,25-/m1/s1
| SMILES = CC(C)(CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)O4((((O4)CO)O)O)O)O
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| InChI = 1/C26H30O12/c1-26(2,35)8-7-13-15(36-25-22(34)20(32)18(30)16(10-27)37-25)9-14(29)17-19(31)21(33)23(38-24(13)17)11-3-5-12(28)6-4-11/h3-6,9,16,18,20,22,25,27-30,32-35H,7-8,10H2,1-2H3/t16-,18-,20+,22-,25-/m1/s1
| StdInChIKey = UNHHWEHQUUGKEE-BGCJFSMVSA-N
| InChIKey = UNHHWEHQUUGKEE-MLLLWRCABA
| CASNo_Ref = {{cascite|correct|??}}
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| CASNo = <!-- blanked - oldvalue: 641-94-1 -->
| StdInChI = 1S/C26H30O12/c1-26(2,35)8-7-13-15(36-25-22(34)20(32)18(30)16(10-27)37-25)9-14(29)17-19(31)21(33)23(38-24(13)17)11-3-5-12(28)6-4-11/h3-6,9,16,18,20,22,25,27-30,32-35H,7-8,10H2,1-2H3/t16-,18-,20+,22-,25-/m1/s1
| PubChem = 5318156
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| SMILES = CC(C)(CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O<br>CC(C)(CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)O4((((O4)CO)O)O)O)O
| StdInChIKey = UNHHWEHQUUGKEE-MLLLWRCASA-N
| CASNo_Ref = {{cascite|changed|??}}
| CASNo = 641-94-1
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = F3862WT2AZ
| PubChem = 5318156
}} }}
|Section2= {{Chembox Properties |Section2={{Chembox Properties
| Formula = C<sub>26</sub>H<sub>30</sub>O<sub>12</sub> | Formula = C<sub>26</sub>H<sub>30</sub>O<sub>12</sub>
| MolarMass = 534.50 g/mol | MolarMass = 534.50 g/mol
| Appearance =
| ExactMass = 534.173726
| Density = 1.581 g/mL
| Appearance =
| Density = | MeltingPt =
| MeltingPt = | BoilingPt =
| BoilingPt = | Solubility =
| Solubility =
}} }}
|Section3= {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}
'''Amurensin''' is a ], a type of flavonoid. It is the ] derivative of ]. It can be found in '']''.<ref>Two New Flavonoid Glycosides from the Leaves of Phellodendron amurense Ruprecht. Masao Hasegawa and Teruo Shirato, J. Am. Chem. Soc., 1953, 75 (22), pages 5507–5511, {{doi|10.1021/ja01118a013}}</ref>

<!-- ==Uses==
can act as an -->

<!--==Metabolism==
The enzyme [[ -->

== Related compounds ==
] is found in the leaves of '']''.<ref>Constituents of Leaves of Phellodendron japonicum MAXIM. and Their Antioxidant Activity, Chih-Yang Chiu, Chia-Ying Li, Chao-Chen Chiu, Masatake Niwa, Susumu Kitanaka, Amooru Gangaiah Damu, E-Jian Lee and Tian-Shung Wu, Chem. Pharm. Bull., Vol. 53, pages 1118-1121 (2005), {{doi|10.1248/cpb.53.1118}}</ref>

== References ==
{{reflist}}

{{Flavonol}}

]
]
]
]
]
]

{{Aromatic-stub}}