Results 181 to 190 of about 17,219 (233)
Secreted proteins of <i>Mycobacterium tuberculosis</i> as therapeutic targets for drug discovery. [PDF]
Kaweesa AM, Tiwari D.
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Multifaceted Anticancer Activity of Flavanone/Chromanone Intermediates for Five-Membered Heterocyclic Derivatives: Targeting Oxidative Stress, Apoptosis, and MAPK Signaling in Colorectal Cancer. [PDF]
Hikisz P, Adamus-Grabicka AA, Budzisz E.
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Phytochemical diversity and antioxidant capacity of citrus cultivars in Zhejiang: a phenolic profiling study for resource evaluation and differentiation. [PDF]
Zhang W +7 more
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The photochemistry of flavanone
Journal of the Chemical Society, Chemical Communications, 1972On u.v. irradiation, flavanone rearranges to 4-phenyldihydrocoumarin and 2′-hydroxychalcone, and undergoes fragmentation to yield a highly reactive keto-keten.
P. O. L. Mack, J. T. Pinhey
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An Improved Method for the Synthesis of Flavanones
Russian Journal of Bioorganic Chemistry, 2002An isomerization of 2'-hydroxychalcones into the corresponding flavanones in ethanol in the presence of triethylamine is described.
A, Aĭtmambetov, A A, Kubzheterova
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Enzymatic halogenation of flavanones and flavones
Phytochemistry, 2001The whole cells and the chloroperoxidase enzyme of Caldariomyces fumago were capable of halogenating the flavanones, naringenin and hesperetin, at C-6 and C-8 in the presence of either Cl- or Br-. However, they did not act on other test flavones. The biohalogenated products of naringenin and hesperetin were isolated and found to be identical to those ...
P, Yaipakdee, L W, Robertson
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The biliary excretion of flavanones in the rat
Xenobiotica, 19791. The major biliary metabolites of flavanones in the rat have been identified by chromatographic and spectral methods. 2. Evidence is presented that flavanones and flavanone glycosides, following oral or parenteral administration, undergo glucuronylation and are selectively excreted via the bile. 3.
A M, Hackett +3 more
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Efficient Synthesis of Flavanone Glucuronides
Journal of Agricultural and Food Chemistry, 2009The first efficient synthesis of flavanone glucuronides as potential human metabolites is described. The synthetic strategy is based on acetyl protection, followed by a combination of chemical and enzymatic deprotection steps. As an example, the method is applied to a synthesis of 7,4'-di-O-methyleriodictyol 3'-O-beta-d-glucuronide.
Ahcene, Boumendjel +3 more
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