[] | , , , , , , . C-glycosylflavones from Oryza sativa. Phytochemistry, 1985, 24: 1061-1064. |
[] | , . Metabolic engineering of the flavone-C-glycoside pathway using polyprotein technology. Metab Eng, 2013, 16: 11-20. |
[] | , , , , , , , , , , . Probing and engineering key residues for bis-C-glycosylation and promiscuity of a C-glycosyltransferase. ACS Catal, 2018, 8: 4917-4927. |
[] | , , , , , , , . Impact of edaphic factors and nutrient management on the hepatoprotective efficiency of carlinoside purified from pigeon pea leaves: An evaluation of UGT1A1 activity in hepatitis induced organelles. Environ Res, 2018, 161: 512-523. |
[] | , , . Structure-based virtual screening of a natural product database to identify several possible SARS-CoV-2 main protease inhibitors. ChemRxiv, 2020 |
[] | , , , , , , , , , . Enzymatic basis for stepwise C-glycosylation in the formation of flavonoid di-C-glycosides in sacred lotus (Nelumbo nucifera Gaertn.). Plant J, 2021, 106: 351-365. |
[] | , , . Biosynthesis of UDP-xylose and UDP-arabinose in Sinorhizobium meliloti 1021: first characterization of a bacterial UDP-xylose synthase, and UDP-xylose 4-epimerase. Microbiol, 2011, 157: 260-269. |
[] | , , , , , , , , , . Molecular and structural characterization of a promiscuous C-glycosyltransferase from Trollius chinensis. Angew Chem Int Ed, 2019, 58: 11513-11520. |
[] | , , , , , , , . Isoschaftoside, a C-glycosylflavonoid from Desmodium uncinatum root exudate, is an allelochemical against the development of Striga. Phytochemistry, 2010, 71: 904-908. |
[] | , , , . Production of C-glucosides of flavonoids and related compounds by Escherichia coli expressing buckwheat C-glucosyltransferase. Plant Biotechnol, 2014, 31: 519-524. |
[] | , , , , , , . In silico screening of natural compounds against COVID-19 by targeting Mpro and ACE2 using molecular docking. Eur Rev Med Pharmacol Sci, 2020, 24: 4529-4536. |
[] | , , , , . Metabolic engineering of Escherichia coli for the biosynthesis of flavonoid-O-glucuronides and flavonoid-O-galactoside. Appl Microbiol Biotechnol, 2015, 99: 2233-2242. |
[] | , , , , , , . Identification and quantification of flavonoids in yellow grain mutant of rice (Oryza sativa L.). Food Chem, 2018, 241: 154-162. |
[] | , , , , , , , , , , , , , , , . Anti-melanogenic activity of schaftoside in Rhizoma Arisaematis by increasing autophagy in B16F1 cells. Biochem Biophys Res Commun, 2018, 503: 309-315. |
[] | , , , , , . Production of plant-specific flavones baicalein and scutellarein in an engineered E. coli from available phenylalanine and tyrosine. Metab Eng, 2019, 52: 124-133. |
[] | , , , , , , . Development of a recombinant Escherichia coli strain for overproduction of the plant pigment anthocyanin. Appl Environ Microbiol, 2015, 81: 6276-6284. |
[] | , , , , , , . Prevention of cholesterol gallstone disease by schaftoside in lithogenic diet-induced C57BL/6 mouse model. Eur J Pharmacol, 2017, 815: 1-9. |
[] | , , , , , , , , , , , , , , , , , , . Engineering yeast for the production of breviscapine by genomic analysis and synthetic biology approaches. Nat Commun, 2018, 9: 448. |
[] | , , , . Regiospecific modifications of naringenin for astragalin production in Escherichia coli. Biotechnol Bioeng, 2013, 110: 2525-2535. |
[] | , , , , , , , . C-glycosylflavones from the aerial parts of Eleusine indica inhibit LPS-induced mouse lung inflammation. Planta Med, 2005, 71: 362-363. |
[] | , , , , . Production of 3-O-xylosyl quercetin in Escherichia coli. Appl Microbiol Biotechnol, 2013, 97: 1889-1901. |
[] | , , , , , , , . Metabolic engineering of Escherichia coli for astragalin biosynthesis. J Agric Food Chem, 2016, 64: 7966-7972. |
[] | , , , . Natural product C-glycosyltransferases—a scarcely characterised enzymatic activity with biotechnological potential. Nat Prod Rep, 2021, 38: 432-443. |
[] | , , , . Chemical studies on novel rice hull antioxidants. 2. Identification of isovitexin, a C-glycosyl flavonoid. J Agric Food Chem, 1989, 37: 316-319. |
[] | , , , , . Identification of a Saccharomyces cerevisiae glucosidase that hydrolyzes flavonoid glucosides. Appl Environ Microbiol, 2011, 77: 1751-1757. |
[] | , , , , . Biosynthesis of flavone C-glucosides in engineered Escherichia coli. Appl Microbiol Biotechnol, 2018, 102: 1251-1267. |
[] | , , . Genetic engineering approach for the production of rhamnosyl and allosyl flavonoids from Escherichia coli. Biotechnol Bioeng, 2010, 107: 154-162. |
[] | , , , . Schaftosides from rice phloem as feeding inhibitors and resistance factors to brown planthoppers, Nilaparvata lugens. Entomol Exp Appl, 1996, 80: 246-249. |
[] | , , , , , , , , . Pathway-specific enzymes from bamboo and crop leaves biosynthesize anti-nociceptive C-glycosylated flavones. Commun Biol, 2020, 3: 110. |
[] | , . Advances in C-glycosylflavonoid Research. Curr Org Chem, 2012, 16: 859-896. |
[] | , , , , , . Indirect and direct routes to C-glycosylated flavones in Saccharomyces cerevisiae. Microb Cell Fact, 2018, 17: 107. |
[] | , , , , , , , , , , , , . Dissection of the general two-step di-C-glycosylation pathway for the biosynthesis of (iso)schaftosides in higher plants. Proc Natl Acad Sci USA, 2020, 117: 30816-30823. |
[] | , , , , , . Metabolome analysis of Oryza sativa (rice) using liquid chromatography-mass spectrometry for characterizing organ specificity of flavonoids with anti-inflammatory and anti-oxidant activity. Chem Pharm Bull, 2016, 64: 952-956. |
[] | , , , , , , , , , , , , , , , , , . Functional characterization and structural basis of an efficient di-C-glycosyltransferase from Glycyrrhiza glabra. J Am Chem Soc, 2020, 142: 3506-3512. |