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5-O-Methylmyricetin: Difference between revisions

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| ImageName = Chemical structure of 5-''O''-methylmyricetin | ImageName = Chemical structure of 5-''O''-methylmyricetin
| IUPACName = 3,3′,4′,5′,7-Pentahydroxy-5-methoxyflavone | IUPACName = 3,3′,4′,5′,7-Pentahydroxy-5-methoxyflavone
| PIN = 3,7-Dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)-4''H''-1-benzopyran-4-one | SystematicName = 3,7-Dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)-4''H''-1-benzopyran-4-one
| OtherNames = 5-Methylmyricetin | OtherNames = 5-Methylmyricetin
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
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}} }}


'''5-''O''-Methylmyricetin''' is an ], a type of ]. It is the 5-''O''-] derivative of ]. It occurs naturally and can also be synthetized.<ref>{{cite journal | title = Synthesis of naturally occurring partial methyl ethers of myricetin | author = P. N. Sarma, G. Srimannarayana and N. V. Subba Rao | journal = Proceedings Mathematical Sciences | volume = 80 | issue = 4 | pages = 168–173 | year = 1974| doi = 10.1007/BF03046674 | s2cid = 92325935 }}</ref> '''5-''O''-Methylmyricetin''' is an ], a type of ]. It is the 5-''O''-] derivative of ]. It occurs naturally and can also be synthesized.<ref>{{cite journal | title = Synthesis of naturally occurring partial methyl ethers of myricetin | author = P. N. Sarma, G. Srimannarayana and N. V. Subba Rao | journal = Proceedings Mathematical Sciences | volume = 80 | issue = 4 | pages = 168–173 | year = 1974| doi = 10.1007/BF03046674 | s2cid = 92325935 }}</ref>


== References == == References ==
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{{DEFAULTSORT:Methylmyricetin, 5-O-}} {{DEFAULTSORT:Methylmyricetin, 5-O-}}
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Latest revision as of 16:09, 27 April 2023

5-O-Methylmyricetin
Chemical structure of 5-O-methylmyricetin
Names
IUPAC name 3,3′,4′,5′,7-Pentahydroxy-5-methoxyflavone
Systematic IUPAC name 3,7-Dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
Other names 5-Methylmyricetin
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3Key: DDVGNSDGGWHPQZ-UHFFFAOYSA-N
  • InChI=1/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3Key: DDVGNSDGGWHPQZ-UHFFFAOYAT
SMILES
  • COC1=C2C(=CC(=C1)O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O
  • O=C1c3c(O/C(=C1/O)c2cc(O)c(O)c(O)c2)cc(O)cc3OC
Properties
Chemical formula C16H12O8
Molar mass 332.264 g·mol
Density 1.731 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

5-O-Methylmyricetin is an O-methylated flavonol, a type of flavonoid. It is the 5-O-methyl derivative of myricetin. It occurs naturally and can also be synthesized.

References

  1. P. N. Sarma, G. Srimannarayana and N. V. Subba Rao (1974). "Synthesis of naturally occurring partial methyl ethers of myricetin". Proceedings Mathematical Sciences. 80 (4): 168–173. doi:10.1007/BF03046674. S2CID 92325935.
Flavonols and their conjugates
Backbone
Aglycones
Flavonols
Aglycones
Conjugates
Glycosides of herbacetin
Glycosides of kaempferol
Glycosides of myricetin
Conjugates of quercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
other
Derivative flavonols
Aglycones
Glycosides
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
Glycosides
Semisynthetic
Glycosides
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