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Structural basis for the promiscuous biosynthetic prenylation of aromatic natural productsXanthones of Lichen Source: A 2016 UpdateThe ABBA family of aromatic prenyltransferases: broadening natural product diversitySynthetic biology approaches in drug discovery and pharmaceutical biotechnology.Artocarpin, an isoprenyl flavonoid, induces p53-dependent or independent apoptosis via ROS-mediated MAPKs and Akt activation in non-small cell lung cancer cells.A new Prenylated Flavonoid induces G0/G1 arrest and apoptosis through p38/JNK MAPK pathways in Human Hepatocellular Carcinoma cells.Prevention of disuse muscle atrophy by dietary ingestion of 8-prenylnaringenin in denervated mice.Reverse prenyltransferase in the biosynthesis of fumigaclavine C in Aspergillus fumigatus: gene expression, purification, and characterization of fumigaclavine C synthase FGAPT1.Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part II: Reconstruction of multienzyme pathways in plants and microbes.Molecular characterization and phylogenetic analysis of two novel regio-specific flavonoid prenyltransferases from Morus alba and Cudrania tricuspidata.Potential of a 7-dimethylallyltryptophan synthase as a tool for production of prenylated indole derivatives.Artocarpin Induces Apoptosis in Human Cutaneous Squamous Cell Carcinoma HSC-1 Cells and Its Cytotoxic Activity Is Dependent on Protein-Nutrient Concentration.Minor Prenylated Flavonoids from the Twigs of Macarangaadenantha and Their Cytotoxic ActivityExpression, purification, crystallization and crystallographic study of the Aspergillus terreus aromatic prenyltransferase AtaPT.Isoprenylated Flavonoids with PTP1B Inhibition from Macaranga denticulata.Regiospecific synthesis of prenylated flavonoids by a prenyltransferase cloned from Fusarium oxysporumBioactive constituents of Indigofera spicata.Molecular Characterization of Soybean Pterocarpan 2-Dimethylallyltransferase in Glyceollin Biosynthesis: Local Gene and Whole-Genome Duplications of Prenyltransferase Genes Led to the Structural Diversity of Soybean Prenylated Isoflavonoids.Direct Assembly of Prenylated Heteroarenes through a Cascade Minisci Reaction/Dehydration Sequence.Palladium-catalyzed completely linear-selective Negishi cross-coupling of allylzinc halides with aryl and vinyl electrophilesPrenylated isoflavonoids from plants as selective estrogen receptor modulators (phytoSERMs).A systematic review on biological activities of prenylated flavonoids.Phytochemical regulation of Fyn and AMPK signaling circuitry.Impacts and perspectives of prenyltransferases of the DMATS superfamily for use in biotechnology.Inhibition of gingipains and Porphyromonas gingivalis growth and biofilm formation by prenyl flavonoids.PrenDB, a Substrate Prediction Database to Enable Biocatalytic Use of Prenyltransferases.Synthesis of a natural chalcone and its prenyl analogs--evaluation of tumor cell growth-inhibitory activities, and effects on cell cycle and apoptosis.Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities.Synthesis and Evaluation of Novel Oxyalkylated Derivatives of 2',4'-Dihydroxychalcone as Anti-Oomycete Agents against Bronopol Resistant Strains of Saprolegnia sp.Prenylflavonoid Isoxanthohumol Sensitizes MCF-7/ADR Cells to Doxorubicin Cytotoxicity via Acting as a Substrate of ABCB1.Synthesis of prenylated flavonols and their potents as estrogen receptor modulator.Site-directed mutagenesis switching a dimethylallyl tryptophan synthase to a specific tyrosine C3-prenylating enzyme.Bavachinin, as a novel natural pan-PPAR agonist, exhibits unique synergistic effects with synthetic PPAR-γ and PPAR-α agonists on carbohydrate and lipid metabolism in db/db and diet-induced obese mice.Reconstruction of pyrrolo[2,3-b]indoles carrying an alpha-configured reverse C3-dimethylallyl moiety by using recombinant enzymes.A rapid screening method for prenylated flavonoids with ultra-high-performance liquid chromatography/electrospray ionisation mass spectrometry in licorice root extracts.A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation.AuaA, a membrane-bound farnesyltransferase from Stigmatella aurantiaca, catalyzes the prenylation of 2-methyl-4-hydroxyquinoline in the biosynthesis of aurachins.Antiparasitic activity of C-geranyl flavonoids from Mimulus bigelovii.Design, synthesis, and biological evaluation of prenylated chalcones as vasorelaxant agents.A new member of the DMATS superfamily from Aspergillus niger catalyzes prenylations of both tyrosine and tryptophan derivatives.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Prenylated flavonoids: pharmacology and biotechnology.
@ast
Prenylated flavonoids: pharmacology and biotechnology.
@en
type
label
Prenylated flavonoids: pharmacology and biotechnology.
@ast
Prenylated flavonoids: pharmacology and biotechnology.
@en
prefLabel
Prenylated flavonoids: pharmacology and biotechnology.
@ast
Prenylated flavonoids: pharmacology and biotechnology.
@en
P2093
P356
P1476
Prenylated flavonoids: pharmacology and biotechnology.
@en
P2093
Alberto Vitali
Bruno Botta
Domenico Misiti
Giuliano Delle Monache
Pilar Menendez
P304
P356
10.2174/0929867053202241
P577
2005-01-01T00:00:00Z