Flavones (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Flavones" in English language version.

refsWebsite

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13doi.org

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12nih.gov

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6semanticscholar.org

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1oregonstate.edu

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1chemspider.com

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1eurekalert.org

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1googlepages.com

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1web.archive.org

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1handle.net

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1archives-ouvertes.fr

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1worldcat.org

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archives-ouvertes.fr

hal.archives-ouvertes.fr

Larget R, Lockhart B, Renard P, Largeron M (April 2000). "A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro" (PDF). Bioorg. Med. Chem. Lett. 10 (8): 835–8. doi:10.1016/S0960-894X(00)00110-4. PMID 10782697.

chemspider.com

"Flavone". ChemSpider, Royal Society of Chemistry. 2015. Retrieved 30 March 2018.

doi.org

Cermak R, Wolffram S (Oct 2006). "The potential of flavonoids to influence drug metabolism and pharmacokinetics by local gastrointestinal mechanisms". Curr Drug Metab. 7 (7): 729–744. doi:10.2174/138920006778520570. PMID 17073577.
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. S2CID 285706.[1] Archived 2008-12-17 at the Wayback Machine
Ferrer JL, Austin MB (2008). "Structure and function of enzymes involved in the biosynthesis of phenylpropanoids". Plant Physiol. Biochem. 46 (3): 356–370. doi:10.1016/j.plaphy.2007.12.009. PMC 2860624. PMID 18272377.
Mizutani M, Ohta D, Sato R (1997). "Isolation of a cDNA and a genomic clone encoding cinnamate 4-hydroxylase from Arabidopsis and its expression manner in plants". Plant Physiology. 113 (3): 755–763. doi:10.1104/pp.113.3.755. PMC 158193. PMID 9085571. S2CID 10059931.
Ferrer JL, Jez JM (1999). "Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis". Nat. Struct. Biol. 6 (8): 775–784. doi:10.1038/11553. PMID 10426957. S2CID 23408591.
Jez JM, Bowman ME (2000). "Structure and mechanism of the evolutionarily unique plany enzyme chalcone isomerase". Nat. Struct. Biol. 7 (9): 786–791. doi:10.1038/79025. PMID 10966651. S2CID 22198011.
Martens S, Mithofer A (2005). "Flavones and flavone synthases". Phytochemistry. 66 (20): 2399–2407. doi:10.1016/j.phytochem.2005.07.013. PMID 16137727.
Sarda SR, Pathan MY, Paike VV, Pachmase PR, Jadhav WN, Pawar RP (2006). "A facile synthesis of flavones using recyclable ionic liquid under microwave irradiation". Arkivoc. xvi (16): 43–8. doi:10.3998/ark.5550190.0007.g05. hdl:2027/spo.5550190.0007.g05.
Wessely F, Moser GH (December 1930). "Synthese und Konstitution des Skutellareins". Monatshefte für Chemie. 56 (1): 97–105. doi:10.1007/BF02716040. S2CID 95833443.
Larget R, Lockhart B, Renard P, Largeron M (April 2000). "A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro" (PDF). Bioorg. Med. Chem. Lett. 10 (8): 835–8. doi:10.1016/S0960-894X(00)00110-4. PMID 10782697.
Harborne, Jeffrey B.; Marby, Helga; Marby, T. J. (1975). The Flavonoids - Springer. doi:10.1007/978-1-4899-2909-9. ISBN 978-0-12-324602-8. S2CID 33487001.
Dewick, Paul M. (2009). "The Shikimate Pathway: Aromatic Amino Acids and Phenylpropanoids". Medicinal Natural Products. A Biosynthetic Approach. Chichester, UK: John Wiley & Sons. pp. 137–186. doi:10.1002/9780470742761.ch4. ISBN 978-0-470-74276-1.
Yeh, Tian-Shin; Yuan, Changzheng; Ascherio, Alberto; Rosner, Bernard A.; Willett, Walter C.; Blacker, Deborah (2021-09-07). "Long-term Dietary Flavonoid Intake and Subjective Cognitive Decline in US Men and Women". Neurology. 97 (10): e1041–e1056. doi:10.1212/WNL.0000000000012454. ISSN 0028-3878. PMC 8448553. PMID 34321362.

eurekalert.org

David Stauth (5 March 2007). "Studies force new view on biology of flavonoids". EurekAlert!; Adapted from a news release issued by Oregon State University.

googlepages.com

p4502c.googlepages.com

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. S2CID 285706.[1] Archived 2008-12-17 at the Wayback Machine

handle.net

hdl.handle.net

Sarda SR, Pathan MY, Paike VV, Pachmase PR, Jadhav WN, Pawar RP (2006). "A facile synthesis of flavones using recyclable ionic liquid under microwave irradiation". Arkivoc. xvi (16): 43–8. doi:10.3998/ark.5550190.0007.g05. hdl:2027/spo.5550190.0007.g05.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cermak R, Wolffram S (Oct 2006). "The potential of flavonoids to influence drug metabolism and pharmacokinetics by local gastrointestinal mechanisms". Curr Drug Metab. 7 (7): 729–744. doi:10.2174/138920006778520570. PMID 17073577.
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. S2CID 285706.[1] Archived 2008-12-17 at the Wayback Machine
Ferrer JL, Austin MB (2008). "Structure and function of enzymes involved in the biosynthesis of phenylpropanoids". Plant Physiol. Biochem. 46 (3): 356–370. doi:10.1016/j.plaphy.2007.12.009. PMC 2860624. PMID 18272377.
Mizutani M, Ohta D, Sato R (1997). "Isolation of a cDNA and a genomic clone encoding cinnamate 4-hydroxylase from Arabidopsis and its expression manner in plants". Plant Physiology. 113 (3): 755–763. doi:10.1104/pp.113.3.755. PMC 158193. PMID 9085571. S2CID 10059931.
Ferrer JL, Jez JM (1999). "Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis". Nat. Struct. Biol. 6 (8): 775–784. doi:10.1038/11553. PMID 10426957. S2CID 23408591.
Jez JM, Bowman ME (2000). "Structure and mechanism of the evolutionarily unique plany enzyme chalcone isomerase". Nat. Struct. Biol. 7 (9): 786–791. doi:10.1038/79025. PMID 10966651. S2CID 22198011.
Martens S, Mithofer A (2005). "Flavones and flavone synthases". Phytochemistry. 66 (20): 2399–2407. doi:10.1016/j.phytochem.2005.07.013. PMID 16137727.
Larget R, Lockhart B, Renard P, Largeron M (April 2000). "A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro" (PDF). Bioorg. Med. Chem. Lett. 10 (8): 835–8. doi:10.1016/S0960-894X(00)00110-4. PMID 10782697.
Yeh, Tian-Shin; Yuan, Changzheng; Ascherio, Alberto; Rosner, Bernard A.; Willett, Walter C.; Blacker, Deborah (2021-09-07). "Long-term Dietary Flavonoid Intake and Subjective Cognitive Decline in US Men and Women". Neurology. 97 (10): e1041–e1056. doi:10.1212/WNL.0000000000012454. ISSN 0028-3878. PMC 8448553. PMID 34321362.

ncbi.nlm.nih.gov

Ferrer JL, Austin MB (2008). "Structure and function of enzymes involved in the biosynthesis of phenylpropanoids". Plant Physiol. Biochem. 46 (3): 356–370. doi:10.1016/j.plaphy.2007.12.009. PMC 2860624. PMID 18272377.
Mizutani M, Ohta D, Sato R (1997). "Isolation of a cDNA and a genomic clone encoding cinnamate 4-hydroxylase from Arabidopsis and its expression manner in plants". Plant Physiology. 113 (3): 755–763. doi:10.1104/pp.113.3.755. PMC 158193. PMID 9085571. S2CID 10059931.
Yeh, Tian-Shin; Yuan, Changzheng; Ascherio, Alberto; Rosner, Bernard A.; Willett, Walter C.; Blacker, Deborah (2021-09-07). "Long-term Dietary Flavonoid Intake and Subjective Cognitive Decline in US Men and Women". Neurology. 97 (10): e1041–e1056. doi:10.1212/WNL.0000000000012454. ISSN 0028-3878. PMC 8448553. PMID 34321362.

oregonstate.edu

lpi.oregonstate.edu

"Flavonoids". Micronutrient Information Center, Linus Pauling Institute, Oregon State University, Corvallis, OR. November 2015. Retrieved 30 March 2018.

semanticscholar.org

api.semanticscholar.org

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. S2CID 285706.[1] Archived 2008-12-17 at the Wayback Machine
Mizutani M, Ohta D, Sato R (1997). "Isolation of a cDNA and a genomic clone encoding cinnamate 4-hydroxylase from Arabidopsis and its expression manner in plants". Plant Physiology. 113 (3): 755–763. doi:10.1104/pp.113.3.755. PMC 158193. PMID 9085571. S2CID 10059931.
Ferrer JL, Jez JM (1999). "Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis". Nat. Struct. Biol. 6 (8): 775–784. doi:10.1038/11553. PMID 10426957. S2CID 23408591.
Jez JM, Bowman ME (2000). "Structure and mechanism of the evolutionarily unique plany enzyme chalcone isomerase". Nat. Struct. Biol. 7 (9): 786–791. doi:10.1038/79025. PMID 10966651. S2CID 22198011.
Wessely F, Moser GH (December 1930). "Synthese und Konstitution des Skutellareins". Monatshefte für Chemie. 56 (1): 97–105. doi:10.1007/BF02716040. S2CID 95833443.
Harborne, Jeffrey B.; Marby, Helga; Marby, T. J. (1975). The Flavonoids - Springer. doi:10.1007/978-1-4899-2909-9. ISBN 978-0-12-324602-8. S2CID 33487001.

web.archive.org

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. S2CID 285706.[1] Archived 2008-12-17 at the Wayback Machine

worldcat.org

search.worldcat.org

Yeh, Tian-Shin; Yuan, Changzheng; Ascherio, Alberto; Rosner, Bernard A.; Willett, Walter C.; Blacker, Deborah (2021-09-07). "Long-term Dietary Flavonoid Intake and Subjective Cognitive Decline in US Men and Women". Neurology. 97 (10): e1041–e1056. doi:10.1212/WNL.0000000000012454. ISSN 0028-3878. PMC 8448553. PMID 34321362.