The following flavonoids were used in this study: biochanin A (>98%, Tokyo Chemical Industry, B4098), (+)-catechin hydrate (98%, Tokyo Chemical Industry, C0705), chrysin (98%, Alfa Aesar, L14178), cyanidin chloride (98%, Fujifilm Wako Chemicals, 030-21961), daidzein (DAI; ≥98%, Nagara Science, NH010102), desmethylglycitein (DMG; >95%, Tokyo Chemical Industry, T3473), S-equal (≥97%, Merck, SML2147), fisetin (>96%, Tokyo Chemical Industry, T0121), genistein (>98%, Tokyo Chemical Industry, G0272), 2′-hydroxyflavanone (>98%, Tokyo Chemical Industry, H1024), kaempferol (≥98%, Cayman Chemical Company, 11852), luteolin (95%, Fujifilm Wako Chemicals, 127-06241), myricetin (>97%, Tokyo Chemical Industry, M2131), naringenin (>98%, Alomone Labs, N-110), petunidin (≥98%, Cayman Chemical Company, 19755), quercetin (96.5%, Fujifilm Wako Chemicals, 512-58344), tamarixetin (>99%, Extrasynthese, 1140S), 5,3′,4′-trihydroxyflavone (>85%, Toronto Research Chemicals, T896685), and 7,3′,4′-trihydroxyflavone (>85%, Toronto Research Chemicals, T896780).
Biochanin a
Manufactured by Tokyo Chemical Industry
Sourced in Japan
Biochanin A is a naturally occurring isoflavone compound. It is a crystalline solid and functions as a phytoestrogen, exhibiting structural and functional similarities to the human hormone estrogen.
Automatically generated - may contain errors
Lab products found in correlation
Genistein, by Tokyo Chemical Industry (2 mentions)
Cyanidin chloride, by Fujifilm (1 mentions)
Catechin hydrate, by Tokyo Chemical Industry (1 mentions)
Chrysin, by Thermo Fisher Scientific (1 mentions)
Quercetin, by Fujifilm (1 mentions)
Luteolin, by Fujifilm (1 mentions)
Myricetin, by Tokyo Chemical Industry (1 mentions)
Fisetin, by Tokyo Chemical Industry (1 mentions)
Tamarixetin, by Extrasynthese (1 mentions)
Kaempferol, by Cayman Chemical (1 mentions)
Formononetin, by Tokyo Chemical Industry (1 mentions)
Udp α d glucose, by Merck Group (1 mentions)
Daidzein, by Tokyo Chemical Industry (1 mentions)
Synapt g2 s, by Waters Corporation (1 mentions)
2 protocols using biochanin a
1
Flavonoid Compound Characterization
2
Purification and Characterization of YjiC
Check if the same lab product or an alternative is used in the 5 most similar protocols
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Genistein, daidzein, biochanin A and formononetin were purchased from Tokyo Chemical Industry (Japan). UDP-α-D-glucose was purchased from Sigma-Aldrich (USA). Genistein 7-O-β-D-glucoside (genistin) was available in our laboratory. All other chemicals and reagents were of the highest chemical grade available. The high resolution mass spectrometry spectra were obtained in positive ion mode on ACQUITY (UPLC, Waters Corp., USA) coupled with SYNAPT G2-S (Waters Corp.). The details of the methodology for the cloning, expression, and purification of YjiC are described in our previous report (Pandey et al., 2013a (link)).
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