From Wikipedia, the free encyclopedia
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
|
|
|
|
|
ChemSpider
|
|
|
|
|
|
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 NKey: XUWTZJRCCPNNJR-UHFFFAOYSA-N NInChI=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
|
COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)O)OC)O)OC)O
|
Properties
|
|
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).
|
Chemical compound
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
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.
Flavonols and their conjugates |
---|
Backbone | |
---|
Flavonols | |
---|
O-Methylated flavonols | |
---|
Derivative flavonols | |
---|
Pyranoflavonols | |
---|
Furanoflavonols | |
---|
Semisynthetic | |
---|