Regiospecific Hydrogenation of Bromochalcone by Unconventional Yeast Strains
暂无分享,去创建一个
B. Gawdzik | T. Janeczko | E. Kostrzewa-Susłow | B. Obmińska-Mrukowicz | A. Pawlak | Mateusz Łużny | E. Kozłowska | Alicja Wzorek | Monika Dymarska | Dagmara Kaczanowska
[1] T. Janeczko,et al. Glycosylation of Methylflavonoids in the Cultures of Entomopathogenic Filamentous Fungi as a Tool for Obtaining New Biologically Active Compounds , 2022, International journal of molecular sciences.
[2] Yuri Kim,et al. Neohesperidin Dihydrochalcone and Neohesperidin Dihydrochalcone-O-Glycoside Attenuate Subcutaneous Fat and Lipid Accumulation by Regulating PI3K/AKT/mTOR Pathway In Vivo and In Vitro , 2022, Nutrients.
[3] Ik-Soo Lee,et al. Biotransformation of the Phenolic Constituents from Licorice and Cytotoxicity Evaluation of Their Metabolites , 2021, International journal of molecular sciences.
[4] T. Janeczko,et al. New Glycosylated Dihydrochalcones Obtained by Biotransformation of 2′-Hydroxy-2-methylchalcone in Cultures of Entomopathogenic Filamentous Fungi , 2021, International journal of molecular sciences.
[5] M. Nitschke,et al. Regioselective and chemoselective biotransformation of 2′-hydroxychalcone derivatives by marine-derived fungi , 2021, Biocatalysis and Biotransformation.
[6] F. Allais,et al. Synthesis of Biobased Phloretin Analogues: An Access to Antioxidant and Anti-Tyrosinase Compounds for Cosmetic Applications , 2021, Antioxidants.
[7] T. Janeczko,et al. Highly Effective, Regiospecific Hydrogenation of Methoxychalcone by Yarrowia lipolytica Enables Production of Food Sweeteners , 2020, Catalysts.
[8] T. Janeczko,et al. Chalcone Methoxy Derivatives Exhibit Antiproliferative and Proapoptotic Activity on Canine Lymphoma and Leukemia Cells , 2020, Molecules.
[9] S. Guterres,et al. Dermatological applications of the flavonoid phloretin. , 2020, European journal of pharmacology.
[10] T. Janeczko,et al. Biotransformation of Methoxyflavones by Selected Entomopathogenic Filamentous Fungi , 2020, International journal of molecular sciences.
[11] G. Tasselli,et al. Non-Conventional Yeasts as Sources of Ene-Reductases for the Bioreduction of Chalcones , 2020, Fermentation.
[12] J. Kozłowska,et al. Biotransformation of Hydroxychalcones as a Method of Obtaining Novel and Unpredictable Products Using Whole Cells of Bacteria , 2020, Catalysts.
[13] Agata Bajek-Bil,et al. Dihydrochalcones: Methods of Acquisition and Pharmacological Properties—A First Systematic Review , 2019, Molecules.
[14] A. Hoveyda,et al. Catalytic Enantioselective Addition of an Allyl Group to Ketones Containing a Tri-, a Di-, or a Monohalomethyl Moiety. Stereochemical Control Based on Distinctive Electronic and Steric Attributes of C-Cl, C-Br, and C-F Bonds. , 2019, Journal of the American Chemical Society.
[15] T. Janeczko,et al. Effective Hydrogenation of 3-(2”-furyl)- and 3-(2”-thienyl)-1-(2’-hydroxyphenyl)-prop-2-en-1-one in Selected Yeast Cultures , 2019, Molecules.
[16] D. Wefers,et al. Glucosylation of flavonoids and flavonoid glycosides by mutant dextransucrase from Lactobacillus reuteri TMW 1.106. , 2019, Carbohydrate research.
[17] M. Nitschke,et al. Hydrogenation of Halogenated 2′-Hydroxychalcones by Mycelia of Marine-Derived Fungus Penicillium raistrickii , 2019, Marine Biotechnology.
[18] A. Poliwoda,et al. 'Structural constraints in cyanobacteria-mediated whole-cell biotransformation of methoxylated and methylated derivatives of 2'-hydroxychalcone. , 2019, Journal of biotechnology.
[19] E. David,et al. Pharmacological aspects and potential use of phloretin: a systemic review. , 2019, Mini reviews in medicinal chemistry.
[20] J. Kozłowska,et al. Microbial transformations of 4′-methylchalcones as an efficient method of obtaining novel alcohol and dihydrochalcone derivatives with antimicrobial activity , 2018, RSC advances.
[21] T. Janeczko,et al. Application of α- and β-naphthoflavones as monooxygenase inhibitors of Absidia coerulea KCh 93, Syncephalastrum racemosum KCh 105 and Chaetomium sp. KCh 6651 in transformation of 17α-methyltestosterone. , 2018, Bioorganic chemistry.
[22] Hee-Taik Kang,et al. Novel Neohesperidin Dihydrochalcone Analogue Inhibits Adipogenic Differentiation of Human Adipose-Derived Stem Cells through the Nrf2 Pathway , 2018, International journal of molecular sciences.
[23] A. Poliwoda,et al. Biocatalytic hydrogenation of the C=C bond in the enone unit of hydroxylated chalcones—process arising from cyanobacterial adaptations , 2018, Applied Microbiology and Biotechnology.
[24] Eugene E. Kwan,et al. Concerted Nucleophilic Aromatic Substitutions , 2018, Nature Chemistry.
[25] D. Pinto,et al. Chalcone: A Valuable Scaffold Upgrading by Green Methods , 2017 .
[26] B. Żarowska,et al. Biotechnological methods for chalcone reduction using whole cells of Lactobacillus, Rhodococcus and Rhodotorula strains as a way to produce new derivatives , 2016, Applied Microbiology and Biotechnology.
[27] T. Janeczko,et al. Enantioselective reduction of flavanone and oxidation of cis- and trans-flavan-4-ol by selected yeast cultures , 2014 .
[28] M. Nitschke,et al. Chemoselective reduction of chalcones by whole hyphae of marine fungus Penicillium citrinum CBMAI 1186, free and immobilized on biopolymers , 2014 .
[29] T. Janeczko,et al. Microbial transformations of chalcones to produce food sweetener derivatives , 2013 .
[30] A. Szumny,et al. Microbial synthesis of dihydrochalcones using Rhodococcus and Gordonia species , 2013 .
[31] Naziya Pathan,et al. Stereoselective bioreduction of chalcone and β-diketone by Saccharomyces cerevisiae in biphasic solvent system: A mechanistic study , 2012 .
[32] S. Raimondi,et al. Enoate reductases from non conventional yeasts: bioconversion, cloning, and functional expression in Saccharomyces cerevisiae. , 2011, Journal of biotechnology.
[33] C. Alves,et al. Biotransformation of chalcones by the endophytic fungus Aspergillus flavus isolated from Paspalum maritimum trin , 2011 .
[34] M. G. Nascimento,et al. Efficient chemoselective biohydrogenation of 1,3-diaryl-2-propen-1-ones catalyzed by Saccharomyces cerevisiae yeasts in biphasic system , 2010 .
[35] D. Ferreira,et al. Antioxidant activity of the dihydrochalcones Aspalathin and Nothofagin and their corresponding flavones in relation to other Rooibos ( Aspalathus linearis ) Flavonoids, Epigallocatechin Gallate, and Trolox. , 2009, Journal of agricultural and food chemistry.
[36] J. Pezzuto,et al. Biotransformation of the Chemopreventive Agent 2′,4′,4-Trihydroxychalcone (Isoliquiritigenin) by UDP-Glucuronosyltransferases , 2008, Drug Metabolism and Disposition.
[37] C. Cho,et al. A Ruthenium-Catalyzed One-Pot Method for α-Alkylation of Ketones with Aldehydes. , 2007 .
[38] C. Cho,et al. A ruthenium-catalyzed one-pot method for α-alkylation of ketones with aldehydes , 2006 .
[39] A. Mortensen. Sweeteners permitted in the European Union: safety aspects , 2006 .
[40] A. Braune,et al. Anaerobic Degradation of Flavonoids by Clostridium orbiscindens , 2003, Applied and Environmental Microbiology.
[41] H. Ohta,et al. Selective Hydrogenation of Carbon-Carbon Double bonds of Chalcones by Corynebacterium equi IFO 3730 , 1985 .