Flavonols

Backbone of a flavonol, substituent numbers are indicated.

Flavonols are a class of flavonoids that have the 3-hydroxyflavone backbone (IUPAC name : 3-hydroxy-2-phenylchromen-4-one). Their diversity stems from the different positions of the phenolic -OH groups. They are distinct from flavanols (with "a") such as catechin, another class of flavonoids.

Flavonols are present in a wide variety of fruits and vegetables. In Western populations, estimated daily intake is in the range of 20–50 mg per day for flavonols. Individual intake varies depending on the type of diet consumed.[1]

The phenomenon of dual fluorescence (due to excited state intramolecular proton transfer or ESIPT) is induced by tautomerism of flavonols (and glucosides) and could contribute to plant UV protection and flower colour.[2]

Besides being a subclass of flavonoids (health effects), flavonols are suggested by a study of cranberry juice to play a role along with proanthocyanidins, in the juice's ability to block bacterial adhesion, demonstrated by the compressing the fimbria of E. coli bacteria in the urinary tract so as to greatly reduce the ability of those bacteria to stay put and initiate an infection.[3] Flavonol aglycones in plants are potent antioxidants that serve to protect the plant from reactive oxygen species (ROS).[4]

Flavonols

Flavonols
NameIUPAC name56782'3'4'5'6'
3-Hydroxyflavone3-hydroxy-2-phenylchromen-4-oneHHHHHHHHH
Azaleatin2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxychromen-4-oneOCH3HOHHHHOHOHH
Fisetin3,3',4',7-tetrahydroxy-2-phenylchromen-4-oneHHOHHHOHOHHH
Galangin3,5,7-trihydroxy-2-phenylchromen-4-oneOHHOHHHHHHH
Gossypetin2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxychromen-4-oneOHHOHOHHOHOHHH
Kaempferide3,5,7-trihydroxy-2-(4-methoxyphenyl)chromen-4-oneOHHOHHHHOCH3HH
Kaempferol3,4',5,7-tetrahydroxy-2-phenylchromen-4-oneOHHOHHHHOHHH
Isorhamnetin3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-oneOHHOHHHOCH3OHHH
Morin2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-oneOHHOHHOHHOHHH
Myricetin3,3',4',5',5,7-hexahydroxy-2-phenylchromen-4-oneOHHOHHHOHOHOHH
Natsudaidain2-(3,4-dimethoxyphenyl)-3-hydroxy-5,6,7,8-tetramethoxychromen-4-oneOCH3OCH3OCH3OCH3HHOCH3OCH3H
Pachypodol5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxychromen-4-oneOHHOCH3HHOCH3OHHH
Quercetin3,3',4',5,7-pentahydroxy-2-phenylchromen-4-oneOHHOHHHOHOHHH
Rhamnazin3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxychromen-4-oneOHHOCH3HHOCH3OHHH
Rhamnetin2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-methoxychromen-4-oneOHHOCH3HHOHOHHH

Flavonol glycosides

Flavonols glycosides and acetylated glycosides
NameAglycone356782'3'4'5'6'
AstragalinKaempferolGlc
AzaleinAzaleatinRha
HyperosideQuercetinGal
IsoquercitinQuercetinGlc
KaempferitrinKaempferolRhaRha
MyricitrinMyricetinRha
QuercitrinQuercetinRha
RobininKaempferolRobinoseRha
RutinQuercetinRutinose
SpiraeosideQuercetinGlc
XanthorhamninRhamnetintrisaccharide
AmurensinKaempferolGlctert-amyl
IcariinKaempferideRhaGlctert-amyl
TroxerutinQuercetinRutinosehydroxyethylhydroxyethylhydroxyethyl

Drug interactions

Flavonoids have effects on CYP (P450) activity. Flavonols are inhibitor of CYP2C9 [5] and CYP3A4,[1] which are enzymes that metabolize most drugs in the body.

See also

References

  1. 1 2 Cermak R, Wolffram S (October 2006). "The potential of flavonoids to influence drug metabolism and pharmacokinetics by local gastrointestinal mechanisms". Curr. Drug Metab. 7 (7): 729–44. doi:10.2174/138920006778520570. PMID 17073577.
  2. ↑ Smith, Gerald J.; Markham, Kenneth R. (1998). "Tautomerism of flavonol glucosides: relevance to plant UV protection and flower colour". Journal of Photochemistry and Photobiology A: Chemistry. 118 (2): 99–105. doi:10.1016/s1010-6030(98)00354-2.
  3. ↑ "Juicy news about cranberries". medicalxpress.com. Retrieved 13 April 2018.
  4. ↑ Nakabayashi R1, Yonekura-Sakakibara K, Urano K, Suzuki M, Yamada Y, Nishizawa T, Matsuda F, Kojima M, Sakakibara H, Shinozaki K, Michael AJ, Tohge T, Yamazaki M, Saito K. "Enhancement of oxidative and drought tolerance in Arabidopsis by overaccumulation of antioxidant flavonoids". Plant J. 77 (3): 367–79. doi:10.1111/tpj.12388. PMC 4282528. PMID 24274116.
  5. ↑ Si D, Wang Y, Zhou YH, et al. (March 2009). "Mechanism of CYP2C9 inhibition by flavones and flavonols". Drug Metab. Dispos. 37 (3): 629–34. doi:10.1124/dmd.108.023416. PMID 19074529.
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