Daidzein

Papers

1. Hepatoprotective effects of daidzein against 7,12-dimetylbenz[a]anthracene-induced oxidative stress in mice Choi E.J., and Kim, G.H. Int. J. Mol. Med. 23, 659-664, (2009)

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2. Stimulation of pS2 expression by diet-derived compounds. Sathyamoorthy, N., et al. Cancer Res. 54, 957-961, (1994)

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3. Daidzein inhibits insulin- or insulin-like growth factor-1-mediated signaling in cell cycle progression of Swiss 3T3 cells. Higashi, K. and Ogawara, H. Biochim. Biophys. Acta 1221, 29-35, (1994)

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ADP- and thapsigargin-evoked Ca2+ entry and protein-tyrosine phosphorylation are inhibited by the tyrosine kinase inhibitors genistein and methyl-25-dihydroxycinnamate in fura-2-loaded human platelets. Sargeant, P., et al. J. Biol. Chem. 268, 18151-18156, (1993)

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Secretion of cortisol and aldosterone as a vulnerable target for adrenal endocrine disruption - screening of 30 selected chemicals in the human H295R cell model. Ullerås, E., et al. J. Appl. Toxicol. 28, 1045-53, (2008)

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Screening of Potentially Hormonally Active Chemicals Using Bioluminescent Yeast Bioreporters Sanseverino, J., et al. Toxicol. Sci. 107, 122-34, (2009)

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Dual effects of daidzein on chicken hepatic vitellogenin II expression and estrogen receptor-mediated transactivation in vitro. Ni, Y., et al. Steroids 75, 245-51, (2010)

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Inhibition of Cell Proliferation and MAP Kinase and Akt Pathways in Oral Squamous cell Carcinoma by Genistein and Biochanin A Johnson, T.L., et al. Evid. Based. Complement. Alternat. Med. 7, 351, (2010)

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Enterorhabdus caecimuris sp. nov., a member of the family Coriobacteriaceae isolated from a mouse model of spontaneous colitis, and emended description of the genus Enterorhabdus Clavel et al. 2009 Clavel, T., et al. Int. J. Syst. Evol. Microbiol. 60, 1527-31, (2010)

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A transcript profiling approach reveals an epicatechin-specific glucosyltransferase expressed in the seed coat of Medicago truncatula. Yongzhen Pang et al Proc. Natl. Acad. Sci. U. S. A. 105, 14210-5, (2008)

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Endocrine-immune-paracrine interactions in prostate cells as targeted by phytomedicines. Nora E. Gray et al Cancer Prev. Res. (Phila) 2, 134-42, (2009)

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Structure-based virtual screening for plant-based ERbeta-selective ligands as potential preventative therapy against age-related neurodegenerative diseases. Liqin Zhao et al J. Med. Chem. 48, 3463-6, (2005)

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A new synthesis of isoaurones: cytotoxic activity of compounds related to the alleged structure of isoaurostatin. Eleonora Rizzi et al Bioorg. Med. Chem. Lett. 15, 4313-6, (2005)

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The transgenic Arabidopsis plant system, pER8-GFP, as a powerful tool in searching for natural product estrogen-agonists/antagonists. Fang-Rong Chang et al J. Nat. Prod. 68, 971-3, (2005)

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Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. Deniz Tasdemir et al J. Med. Chem. 49, 3345-53, (2006)

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Osteoblast differentiation stimulating activity of biflavonoids from Cephalotaxus koreana. Mi Kyeong Lee et al Bioorg. Med. Chem. Lett. 16, 2850-4, (2006)

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Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities. Manar M Salem et al J. Nat. Prod. 69, 43-9, (2006)

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Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships. Peter L Katavic et al J. Nat. Prod. 70, 1278-82, (2007)

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Chemical genetics reveals a complex functional ground state of neural stem cells Diamandis, P., et. al. Nat. Chem. Biol. 3(5), 268-273, (2007)

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Expanding the promiscuity of a natural-product glycosyltransferase by directed evolution. Gavin J Williams et al Nat. Chem. Biol. 3, 657-62, (2007)

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Flavonoids for controlling starch digestion: structural requirements for inhibiting human alpha-amylase. Elena Lo Piparo et al J. Med. Chem. 51, 3555-61, (2008)

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Discovery of nonsteroidal 17beta-hydroxysteroid dehydrogenase 1 inhibitors by pharmacophore-based screening of virtual compound libraries. Daniela Schuster et al J. Med. Chem. 51, 4188-99, (2008)

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Structure of daidzin, a naturally occurring anti-alcohol-addiction agent, in complex with human mitochondrial aldehyde dehydrogenase. Edward D Lowe et al J. Med. Chem. 51, 4482-7, (2008)

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ortho-dihydroxyisoflavone derivatives from aged Doenjang (Korean fermented soypaste) and its radical scavenging activity. Jun-Seong Park et al Bioorg. Med. Chem. Lett. 18, 5006-9, (2008)

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Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition. Suresh Awale et al Bioorg. Med. Chem. 16, 181-9, (2008)

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Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship. Feng Li et al Bioorg. Med. Chem. 16, 5434-40, (2008)

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Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities. Ai-Lin Liu et al Bioorg. Med. Chem. 16, 7141-7, (2008)

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Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities. Takuto Kumano et al Bioorg. Med. Chem. 16, 8117-26, (2008)

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Screening of herbal constituents for aromatase inhibitory activity. S Paoletta et al Bioorg. Med. Chem. 16, 8466-70, (2008)

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Antineoplastic agents. 536. New sources of naturally occurring cancer cell growth inhibitors from marine organisms, terrestrial plants, and microorganisms(1a,). George R Pettit et al J. Nat. Prod. 71, 438-44, (2008)

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7-Hydroxy-benzopyran-4-one derivatives: a novel pharmacophore of peroxisome proliferator-activated receptor alpha and -gamma (PPARalpha and gamma) dual agonists. Azadeh Matin et al J. Med. Chem. 52, 6835-50, (2009)

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Effect of flavonoids on androgen and glucocorticoid receptors based on in vitro reporter gene assay. Yosuke Nishizaki et al Bioorg. Med. Chem. Lett. 19, 4706-10, (2009)

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Isoflavones with unusually modified B-rings and their evaluation as antiproliferative agents. B Le S Tchize Ndejouong et al Bioorg. Med. Chem. Lett. 19, 6473-6, (2009)

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Effects of 7-O substitutions on estrogenic and anti-estrogenic activities of daidzein analogues in MCF-7 breast cancer cells. Quan Jiang et al J. Med. Chem. 53, 6153-63, (2010)

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Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors. Jun-Seong Park et al Bioorg. Med. Chem. Lett. 20, 1162-4, (2010)

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Glucose uptake enhancing activity of puerarin and the role of C-glucoside suggested from activity of related compounds. Eisuke Kato et al Bioorg. Med. Chem. Lett. 20, 4333-6, (2010)

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Carboxymethylated-kappa-casein: a convenient tool for the identification of polyphenolic inhibitors of amyloid fibril formation. John A Carver et al Bioorg. Med. Chem. 18, 222-8, (2010)

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Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids. Dragan Ami? et al Bioorg. Med. Chem. 18, 28-35, (2010)

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QSAR study of flavonoids and biflavonoids as influenza H1N1 virus neuraminidase inhibitors. Andrew G Mercader et al Eur. J. Med. Chem. 45, 1724-30, (2010)

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An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds. Yunbao Liu et al J. Nat. Prod. 73, 1193-5, (2010)

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Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells. Hisashi Matsuda et al Bioorg. Med. Chem. 19, 2835-41, (2011)

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Anti-inflammatory principles from Cordyceps sinensis. Mei-Lin Yang et al J. Nat. Prod. 74, 1996-2000, (2011)

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Merck 14,2801

Beil. 18,V,4,89