Jaceidin

Jaceidin
Names
	IUPAC name 4′,5,7-Trihydroxy-3,3′,6-trimethoxyflavone
	Systematic IUPAC name 5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one
	Other names Jaceidine; Quercetagetin 3,3′,6-trimethyl ether
Identifiers
CAS Number	10173-01-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	4576662 ;
PubChem CID	5464461;
CompTox Dashboard (EPA)	DTXSID30144148 ;
	InChI InChI=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 Key: XUWTZJRCCPNNJR-UHFFFAOYSA-N ; 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 Key: XUWTZJRCCPNNJR-UHFFFAOYAP;
	SMILES COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)OC)O;
Properties
Chemical formula	C18H16O8
Molar mass	360.318 g·mol−1
Melting point	130–135 °C (266–275 °F; 403–408 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Jaceidin is an O-methylated flavonol. It can be found in Chamomilla recutita,^[1] in Centaurea jacea and can be synthesized.^[2] 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.^[3]

Glycosides

Jacein

References

^ Repčák, Miroslav; Švehlı́Ková, Vanda; Imrich, Ján; Pihlaja, Kalevi (1999). "Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert". Biochemical Systematics and Ecology. 27 (7): 727–732. doi:10.1016/S0305-1978(98)00124-0.
^ Fukui, K.; Matsumoto, T.; Nakamura, S.; Nakayama, M.; Horie, T. (1968). "The synthesis of jaceidin". Experientia. 24 (2): 108–109. doi:10.1007/BF02146923. PMID 5643784. S2CID 9912322.
^ "Jaceidin". Human Metabolome Database. HMDB0033819.

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[1] Repčák, Miroslav; Švehlı́Ková, Vanda; Imrich, Ján; Pihlaja, Kalevi (1999). "Jaceidin and chrysosplenetin chemotypes of Chamomilla recutita (L.) Rauschert". Biochemical Systematics and Ecology. 27 (7): 727–732. doi:10.1016/S0305-1978(98)00124-0.

[2] Fukui, K.; Matsumoto, T.; Nakamura, S.; Nakayama, M.; Horie, T. (1968). "The synthesis of jaceidin". Experientia. 24 (2): 108–109. doi:10.1007/BF02146923. PMID 5643784. S2CID 9912322.

[3] "Jaceidin". Human Metabolome Database. HMDB0033819.

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