Assessing the Regioselectivity of OleD-Catalyzed Glycosylation with a Diverse Set of Acceptors

Maoquan Zhou, Adel Hamza, Chang-Guo Zhan and Jon S. Thorson

J. Nat. Prod., 2013, 76, 279
DOI: 10.1021/np300890h

X-ray and 13C CP MAS investigations of structure of two genistein derivatives

Grzegorz Grynkiewicz, Oliwia Zegrocka-Stendel, Wiesław Pucko, Jan Ramza, Anna Kościelecka, Wacław Kołodziejski and Krzysztof Woźniak

Journal of Molecular Structure, 2004, 694, 121
DOI: 10.1016/j.molstruc.2004.03.015

NMR as a “Gold Standard” Method in Drug Design and Discovery

Abdul-Hamid Emwas, Kacper Szczepski, Benjamin Gabriel Poulson, Kousik Chandra, Ryan T. McKay, Manel Dhahri, Fatimah Alahmari, Lukasz Jaremko, Joanna Izabela Lachowicz and Mariusz Jaremko

Molecules, 2020, 25, 4597
DOI: 10.3390/molecules25204597

A rapid method for simultaneous determination of 14 phenolic compounds in Radix Puerariae using microwave-assisted extraction and ultra high performance liquid chromatography coupled with diode array detection and time-of-flight mass spectrometry

G. Du, H.Y. Zhao, Q.W. Zhang, G.H. Li, F.Q. Yang, Y. Wang, Y.C. Li and Y.T. Wang

Journal of Chromatography A, 2010, 1217, 705
DOI: 10.1016/j.chroma.2009.12.017

Millettia isoflavonoids: a comprehensive review of structural diversity, extraction, isolation, and pharmacological properties

Kebede Taye Desta and A. M. Abd El-Aty

Phytochem Rev, 2023, 22, 275
DOI: 10.1007/s11101-022-09845-w

An Efficient Method for the Glycosylation of Isoflavones

Nawaf Al‐Maharik and Nigel P. Botting

Eur J Org Chem, 2008, 2008, 5622
DOI: 10.1002/ejoc.200800803

Time-resolved fluoroimmunoassay of plasma daidzein and genistein11Abbreviations: Daidzein (Da), genistein (Gen), gas-liquid chromatography (GC), high performance liquid chromatography (HPLC), mass spectrometry (MS), radioimmunoassay (RIA), time-resolved fluoroimmunoassay (TR-FIA), enzymeimmunoassay (EIA), fluoroimmunoassay (FIA), bovine serum albumin (BSA), N,N′-dicyclohexylcarbodiimide (DCC), N-hydroxysuccinimide (NHS), isotope dilution gas chromatography-mass spectrometry in the selected ion monitoring mode (ID-GC-MS-SIM), coefficients of variation (CVs). B = Binding of tracer to antibody in the presence of unlabeled analyte. B0 = Binding of tracer to antibody in the absence of unlabeled analyte. T = Total amount of tracer added. Estradiol = estradiol-17β.

Guojie J Wang, Oldrich Lapcı́k, Richard Hampl, Mariko Uehara, Nawaf Al–Maharik, Katariina Stumpf, Heikki Mikola, Kristiina Wähälä and Herman Adlercreutz

Steroids, 2000, 65, 339
DOI: 10.1016/S0039-128X(00)00089-1

A New Phenylpropionate Derivative from the Rhizomes of Hedysarum polybotrys

Fan CHENG, Kun ZOU, Shu ZHU and Komatsu KATSUKO

Chinese Journal of Natural Medicines, 2010, 7, 351
DOI: 10.3724/SP.J.1009.2009.00351

Target guided isolation of potential tyrosinase inhibitors from Otholobium pubescens (Poir.) J.W. Grimes by ultrafiltration, high-speed countercurrent chromatography and preparative HPLC

Guanglei Zuo, Zhiqiang Wang, Yanymee N. Guillen Quispe, Seung Hwan Hwang, Hyun Yong Kim, Beom Goo Kang and Soon Sung Lim

Industrial Crops and Products, 2019, 134, 195
DOI: 10.1016/j.indcrop.2019.03.045

Regio- and stereoselective synthesis of the major metabolite of quercetin, quercetin-3-O-β-d-glucuronide

Mohamed Bouktaib, Aziz Atmani and Christian Rolando

Tetrahedron Letters, 2002, 43, 6263
DOI: 10.1016/S0040-4039(02)01264-9

Isoflavone daidzein possesses no antioxidant activities in cell-free assays but induces the antioxidant enzyme catalase

Andreas Kampkötter, Yvonni Chovolou, Andreas Kulawik, Elke Röhrdanz, Nadine Weber, Peter Proksch and Wim Wätjen

Nutrition Research, 2008, 28, 620
DOI: 10.1016/j.nutres.2008.06.002

Highly efficient glucosylation of flavonoids

Volodymyr Semeniuchenko, Yana Garazd, Myroslav Garazd, Tetyana Shokol, Ulrich Groth and Volodymyr Khilya

Monatsh Chem, 2009, 140, 1503
DOI: 10.1007/s00706-009-0207-6

Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A

Sandra Sordon, Jarosław Popłoński, Tomasz Tronina and Ewa Huszcza

Molecules, 2017, 22, 81
DOI: 10.3390/molecules22010081

A new isoflavone glycoside from Pueraria alopecuroides

Junlin Yang, Qingfei Fan, Huanli Zhang and Qishi Song

Natural Product Research, 2016, 30, 100
DOI: 10.1080/14786419.2015.1038813

Bioassay-Guided Characterization, Antioxidant, Anti-Melanogenic and Anti-Photoaging Activities of Pueraria thunbergiana L. Leaf Extracts in Human Epidermal Keratinocytes (HaCaT) Cells

Min Jeong Kim, Seo Yeon Shin, Nu Ri Song, Sunoh Kim, Sang Ouk Sun and Kyung Mok Park

Processes, 2022, 10, 2156
DOI: 10.3390/pr10102156

Total synthesis of apigenin 7,4′-di-O-β-glucopyranoside, a component of blue flower pigment of Salvia patens, and seven chiral analogues

Kin-ichi Oyama and Tadao Kondo

Tetrahedron, 2004, 60, 2025
DOI: 10.1016/j.tet.2004.01.001

Total Synthesis of Quercetin 3-Sophorotrioside

Yuguo Du, Guohua Wei and Robert J. Linhardt

J. Org. Chem., 2004, 69, 2206
DOI: 10.1021/jo035722y

Use of O-glycosylation in total synthesis

Hélène Pellissier

Tetrahedron, 2005, 61, 2947
DOI: 10.1016/j.tet.2005.01.070

Genistein derivatives as selective estrogen receptor modulators: Sonochemical synthesis and in vivo anti-osteoporotic action

Shi F. Wang, Qing Jiang, Yong H. Ye, Yang Li and Ren X. Tan

Bioorganic & Medicinal Chemistry, 2005, 13, 4880
DOI: 10.1016/j.bmc.2005.04.082

AN IMPROVED PHASE TRANSFER CATALYZED SYNTHETIC METHOD FOR ONONIN AND ROTHINDIN

Yaping Wang, Liangxi Li, Qinglian Wang and Yulin Li

Synthetic Communications, 2001, 31, 3423
DOI: 10.1081/SCC-100106200

Phenolic compounds from Pueraria lobata protect PC12 cells against Aβ-induced toxicity

Yun-hyeok Choi, Seong Su Hong, Yu Su Shin, Bang Yeon Hwang, So-Young Park and Dongho Lee

Arch. Pharm. Res., 2010, 33, 1651
DOI: 10.1007/s12272-010-1014-7

Secondary Metabolites from Glycine soja and Their Growth Inhibitory Effect against Spodoptera litura

Yan-Ying Zhou, Shi-Hong Luo, Ting-Shuang Yi, Chun-Huan Li, Qian Luo, Juan Hua, Yan Liu and Sheng-Hong Li

J. Agric. Food Chem., 2011, 59, 6004
DOI: 10.1021/jf200821p

Phytochemical and chemotaxonomic study on Medicago sativa L. (Leguminosae)

Xuegui Liu, Yuqiu Sun, Jun Bian, Mengchao Lv, Ting Han, Haoyue Sun, Danqi Li and Pinyi Gao

Biochemical Systematics and Ecology, 2018, 80, 55
DOI: 10.1016/j.bse.2018.06.008

ChemInform Abstract: The Phase‐Transfer Catalyzed Synthesis of Isoflavone‐O‐glucosides.

P. LEWIS, S. KALTIA and K. WAEHAELAE

ChemInform, 1998, 29
DOI: 10.1002/chin.199852283

Regiospecific 4′-O-β-glucosidation of isoflavones

Philip T. Lewis and Kristiina Wähälä

Tetrahedron Letters, 1998, 39, 9559
DOI: 10.1016/S0040-4039(98)02124-8

Synthesis and Cytotoxic Evaluation of a Series of Genistein Derivatives

Huan‐Qiu Li, Hui‐Ming Ge, Yun‐Xi Chen, Chen Xu, Lei Shi, Hui Ding, Hai‐Liang Zhu and Ren‐Xiang Tan

Chemistry & Biodiversity, 2006, 3, 463
DOI: 10.1002/cbdv.200690049

Microbial Glycosylation of Flavonoids

SANDRA SORDON, JAROSŁAW POPŁOŃSKI and EWA HUSZCZA

Polish Journal of Microbiology, 2016, 65, 137
DOI: 10.5604/17331331.1204473

Synthesis of the Deuterium Labeled Isoflavone-O-glucoside 8,3′,5′-D3-Daidzin

Philip T. Lewis and Kristiina Wähälä

Molecules Online, 1998, 2, 137
DOI: 10.1007/s007830050069

Synthesis ofO‐β‐D‐Glucopyranosides of 7‐Hydroxy‐3‐(imidazol‐2‐yl)‐4H‐chromen‐4‐ones

V. N. Ingle, K. M. Hatzade, V. S. Taile, P. K. Gaidhane and S. T. Kharche

Journal of Carbohydrate Chemistry, 2007, 26, 107
DOI: 10.1080/07328300701298196

Chemical and Enzyme-Assisted Syntheses of Norbuprenorphine-3-β-d-glucuronide

Jinda Fan, Sarah M. Brown, Zhude Tu and Evan D. Kharasch

Bioconjugate Chem., 2011, 22, 752
DOI: 10.1021/bc100550u

Biotransformation of gallic acid by Beauveria sulfurescens ATCC 7159

Feng-Lin Hsu, Li-Ming Yang, Shwu-Fen Chang, Li-Hsuan Wang, Chung-Yi Hsu, Pan-Chun Liu and Shwu-Jiuan Lin

Appl Microbiol Biotechnol, 2007, 74, 659
DOI: 10.1007/s00253-006-0692-z

Synthesis of Selectively Protected Genistein Derivatives

Wiesław Szeja, Gabriela Pastuch, Ilona Wandzik, Nikodem Kuźnik and Grzegorz Grynkiewicz

Synthetic Communications, 2003, 33, 4111
DOI: 10.1081/SCC-120026353

Low-molecular-weight phenolic compounds from Hedysarum theinum roots

I. V. Nechepurenko, M. P. Polovinka, N. I. Komarova, D. V. Korchagina, N. F. Salakhutdinov and S. B. Nechepurenko

Chem Nat Compd, 2008, 44, 31
DOI: 10.1007/s10600-008-0009-9

Regioselective sonochemical synthesis of genistein derivatives

S.F. Wang, Y.H. Ye, Z. Zhang and R.X. Tan

Ultrasonics Sonochemistry, 2006, 13, 28
DOI: 10.1016/j.ultsonch.2004.10.002

High production of genistein diglucoside derivative using cyclodextrin glycosyltransferase from Paenibacillus macerans

Ruizhi Han, Binbin Ge, Mingyang Jiang, Guochao Xu, Jinjun Dong and Ye Ni

Journal of Industrial Microbiology and Biotechnology, 2017, 44, 1343
DOI: 10.1007/s10295-017-1960-x

Isolation and structure elucidation of phenolic compounds from Cyclopia subternata Vogel (honeybush) intact plant and in vitro cultures

Adam Kokotkiewicz, Maria Luczkiewicz, Pawel Sowinski, Daniel Glod, Krzysztof Gorynski and Adam Bucinski

Food Chemistry, 2012, 133, 1373
DOI: 10.1016/j.foodchem.2012.01.114

A facile synthesis of isoflavone 7-O-glucuronides

Nawaf Al-Maharik and Nigel P. Botting

Tetrahedron Letters, 2006, 47, 8703
DOI: 10.1016/j.tetlet.2006.10.034

A new isoflavone derivative from Streptomyces sp. YIM GS3536

Rong Huang, Zhang-Gui Ding, Yun-Feng Long, Jiang-Yuan Zhao, Ming-Gang Li, Xiao-Long Cui and Meng-Liang Wen

Chem Nat Compd, 2013, 48, 966
DOI: 10.1007/s10600-013-0440-4

Phyto-SERM Constitutes from Flemingia macrophylla

Wan-Chun Lai, Ya-Ting Tsui, Abdel Singab, Mohamed El-Shazly, Ying-Chi Du, Tsong-Long Hwang, Chin-Chung Wu, Ming-Hong Yen, Ching-Kuo Lee, Ming-Feng Hou, Yang-Chang Wu and Fang-Rong Chang

IJMS, 2013, 14, 15578
DOI: 10.3390/ijms140815578

Estrogenic and Anti-estrogenic Constituents of Erythrina caffra

Yu-Ming Hsu, Wan-Chun Lai, Chi-Ying Li, Yu-Hsuan Lan, Yu-Chi Tsai, Attila Hunyadi, Ming-Feng Hou, Shyng-Shiou Yuan, Yang-Chang Wu and Fang-Rong Chang

Natural Product Communications, 2016, 11, 1934578X1601100
DOI: 10.1177/1934578X1601100817

Regioselective O-glycosylation of flavonoids by fungi Beauveria bassiana, Absidia coerulea and Absidia glauca

Sandra Sordon, Jarosław Popłoński, Tomasz Tronina and Ewa Huszcza

Bioorganic Chemistry, 2019, 93, 102750
DOI: 10.1016/j.bioorg.2019.01.046

Isolation and characterisation of the isoflavones from sprouted chickpea seeds

Shuhui Zhao, Linping Zhang, Peng Gao and Zhiyu Shao

Food Chemistry, 2009, 114, 869
DOI: 10.1016/j.foodchem.2008.10.026

Rapid simultaneous determination of isoflavones in Radix puerariae using high‐performance liquid chromatography–triple quadrupole mass spectrometry with novel shell‐type column

Gang Du, Haiyu Zhao, Yuelin Song, Qingwen Zhang and Yitao Wang

J of Separation Science, 2011, 34, 2576
DOI: 10.1002/jssc.201100295

Anthranilic Acid Derivatives and Other Components from Ononis pusilla

Lyes Khouni, Christophe Long, Hamada Haba, Nicolas Molinier and Mohammed Benkhaled

Natural Product Communications, 2014, 9, 1934578X1400900
DOI: 10.1177/1934578X1400900825