Flavanone

Manufactured by Fujifilm

Sourced in Japan

Flavanone is a lab equipment product designed for the analysis and identification of flavonoid compounds. It utilizes high-performance liquid chromatography (HPLC) technology to separate and quantify various flavanone derivatives. The core function of Flavanone is to provide accurate and reliable data for researchers and scientists working in fields such as plant chemistry, food science, and pharmaceutical development.

Automatically generated - may contain errors

Lab products found in correlation

Flavone, by Fujifilm (2 mentions) Dimethyl sulfoxide (dmso), by Fujifilm (1 mentions) Epigallocatechin, by Merck Group (1 mentions) Clodronate, by Merck Group (1 mentions) Genistein, by Merck Group (1 mentions) Daidzein, by Fujifilm (1 mentions) Quercetin, by Fujifilm (1 mentions) Apigenin, by Fujifilm (1 mentions) Resveratrol, by Fujifilm (1 mentions) Chrysin, by Fujifilm (1 mentions) Curcumin, by Fujifilm (1 mentions) Ursolic acid, by Fujifilm (1 mentions) Carnosol, by Fujifilm (1 mentions)

2 protocols using flavanone

Cell Proliferation Assays of Food Constituents

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We examined the inhibitory activities of food constituents in cell proliferation assays. Test compounds used in the assays were as follows: curcumin (Wako or Sigma-Aldrich), zerumbone (Wako), genistein (Sigma-Aldrich), chalcone (Wako), corosolic acid (Wako), carnosol (Wako), ursolic acid (Wako), epigallocatechin (Sigma-Aldrich), isoflavone (Wako), apigenin (Wako), chrysin (Wako), flavanone (Wako), resveratrol (Wako), flavone (Wako), quercetin (Wako), daidzein (Wako), and clodronate (Sigma-Aldrich). These compounds were firstly dissolved with dimethyl sulfoxide (DMSO; Wako) and then appropriately diluted with RPMI1640 + 10% FCS to apply the assays. The final concentration of DMSO was adjusted not to exceed 1% at most in cell cultures.

Amano C., Minematsu H., Fujita K., Iwashita S., Adachi M., Igarashi K, & Hinuma S. (2015). Nanoparticles Containing Curcumin Useful for Suppressing Macrophages In Vivo in Mice. PLoS ONE, 10(9), e0137207.

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Flavonoid Oxidation Products Synthesis

Cited 2 times

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Flavone and flavanone (Figure 1) were obtained from Wako Pure Chemicals (Osaka, Japan); the oxidation products 5-, 6-, and 7-hydroxyFlavone (OHF), 5,7-and 7,8-dihydroxyFlavone (diOHF), and 6-and 7-hydroxyflavanone (OHFva) were obtained from Sigma-Aldrich (St. Louis, MO, USA) or Wako Pure Chemicals. 2´-, 3´-, and 4´-Hydroxyflavanones were kindly donated by Dr. Yukinori Yubuta (Tottori University). Other chemicals and reagents used in this study were obtained from the sources described previously or were of the highest quality commercially available (Shimada et al., 2016a (link): 2016b (link)).

Kakimoto K., Murayama N., Takenaka S., Nagayoshi H., Lim Y.R., Kim V., Kim D., Yamazaki H., Komori M., Guengerich F.P, & Shimada T. (2018). Cytochrome P450 2A6 and Other Human P450 Enzymes in the Oxidation of Flavone and Flavanone. Xenobiotica; the fate of foreign compounds in biological systems, 49(2), 131-142.

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