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{{chembox |
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{{chembox |
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| verifiedrevid = 423639727 |
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| verifiedrevid = 447708649 |
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| Name = Jaceidin |
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| Name = Jaceidin |
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| ImageFile = Jaceidin.PNG |
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| ImageFile = Jaceidin.svg |
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| ImageSize = 200px |
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| ImageName = Chemical structure of jaceidin |
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| ImageName = Chemical structure of jaceidin |
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| IUPACName = 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxychromen-4-one |
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| IUPACName = 4′,5,7-Trihydroxy-3,3′,6-trimethoxyflavone |
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| SystematicName = 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4''H''-1-benzopyran-4-one |
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| OtherNames = Jaceidine<br>Quercetagetin 3,3',6-trimethyl ether |
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| OtherNames = Jaceidine<br>Quercetagetin 3,3′,6-trimethyl ether |
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|Section1= {{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo = 10173-01-0 |
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| CASNo = 10173-01-0 |
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| CASNo_Ref = |
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| CASNoOther = |
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| CASOther = |
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| PubChem = 5464461 |
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| PubChem = 5464461 |
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| SMILES = COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)OC)O |
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| SMILES = COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)OC)O |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| InChI = |
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| ChemSpiderID = 4576662 |
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| InChI = 1/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3 |
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| InChIKey = XUWTZJRCCPNNJR-UHFFFAOYAP |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChI = 1S/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3 |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = XUWTZJRCCPNNJR-UHFFFAOYSA-N |
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| MeSHName = |
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|Section2= {{Chembox Properties |
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|Section2={{Chembox Properties |
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| C=18 | H=16 | O=8 |
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| Formula = C<sub>18</sub>H<sub>16</sub>O<sub>8</sub> |
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| MolarMass = 360.31 g/mol |
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| ExactMass = 360.084517 u |
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| Appearance = |
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| Appearance = |
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| Density = |
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| Density = |
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| MeltingPt = <!-- °C --> |
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| MeltingPtC = 130-135 |
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| BoilingPt = <!-- °C --> |
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| BoilingPt = |
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| Solubility = |
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| Solubility = |
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'''Jaceidin''' is an ]. It can be found in '']'',<ref></ref> in '']'' and can be synthetized.<ref></ref> |
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'''Jaceidin''' is an ]. It can be found in '']'',<ref>{{cite journal | doi = 10.1016/S0305-1978(98)00124-0 | title = Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert | journal = Biochemical Systematics and Ecology | volume = 27 | issue = 7 | pages = 727–732 | year = 1999 | last1 = Repčák | first1 = Miroslav | last2 = Švehlı́Ková | first2 = Vanda | last3 = Imrich | first3 = Ján | last4 = Pihlaja | first4 = Kalevi | bibcode = 1999BioSE..27..727R }}</ref> in '']'' and can be synthesized.<ref>{{cite journal | doi = 10.1007/BF02146923 | title = The synthesis of jaceidin | journal = Experientia | volume = 24 | issue = 2 | pages = 108–109 | year = 1968 | last1 = Fukui | first1 = K. | last2 = Matsumoto | first2 = T. | last3 = Nakamura | first3 = S. | last4 = Nakayama | first4 = M. | last5 = Horie | first5 = T. | pmid = 5643784 | s2cid = 9912322 }}</ref> Jaceidin has many different characteristics, such as a molar mass of 360.31 g/mol. It also has a melting point of 130-135 °C.<ref>{{Cite web | url = http://www.hmdb.ca/metabolites/HMDB0033819 | title = Jaceidin | id = HMDB0033819 | work = Human Metabolome Database}}</ref> |
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==Glycosides== |
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== Glycosides == |
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==References== |
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== References == |
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{{reflist}} |
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{{reflist}} |
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{{flavonol}} |
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{{flavonol}} |
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] |
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] |
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{{natural-phenol-stub}} |
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{{aromatic-stub}} |