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Molecular Cloning and Characterization of a cDNA Encoding a Novel Apoplastic Protein Preferentially Expressed in a Shikonin-Producing Callus Strain of Lithospermum erythrorhizon.
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- Plant & Cell Physiology, 2003, v. 44, n. 4, p. 437, doi. 10.1093/pcp/pcg057
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Secondary Metabolites from Phlomis syriaca and Their Antioxidant Activities.
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- Turkish Journal of Chemistry, 2006, v. 30, n. 3, p. 383
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Secondary Metabolites from Phlomis kotschyana.
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- Turkish Journal of Chemistry, 2004, v. 28, n. 6, p. 767
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Chemical Constituents and Antioxidant Activity of Mallotus roxburghianus Leaves.
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- Chemistry & Biodiversity, 2005, v. 2, n. 6, p. 792, doi. 10.1002/cbdv.200590057
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Unusual effects of some vegetable oils on the survival time of stroke-prone spontaneously hypertensive rats.
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- Lipids, 1997, v. 32, n. 7, p. 745, doi. 10.1007/s11745-997-0095-z
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Two unsaturated 9 R-hydroxy fatty acids from the cyanobacterium Anabaena flos-aquae f. flos-aquae.
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- Lipids, 1992, v. 27, n. 10, p. 776, doi. 10.1007/BF02535848
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Application of a quantitative H-NMR (H-qNMR) method for the determination of geniposidic acid and acteoside in Plantaginis semen.
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- Journal of Natural Medicines, 2017, v. 71, n. 1, p. 315, doi. 10.1007/s11418-016-1040-y
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Application of a quantitative H-NMR method for the determination of paeonol in Moutan cortex, Hachimijiogan and Keishibukuryogan.
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- Journal of Natural Medicines, 2016, v. 70, n. 4, p. 797, doi. 10.1007/s11418-016-1003-3
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Application of quantitative H-NMR method to determination of gentiopicroside in Gentianae radix and Gentianae scabrae radix.
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- Journal of Natural Medicines, 2014, v. 68, n. 3, p. 630, doi. 10.1007/s11418-014-0833-0
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Application of a quantitative <sup>1</sup>H-NMR method for the determination of amygdalin in Persicae semen, Armeniacae semen, and Mume fructus.
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- Journal of Natural Medicines, 2014, v. 68, n. 1, p. 225, doi. 10.1007/s11418-013-0783-y
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Calycosin and formononetin from astragalus root enhance dimethylarginine dimethylaminohydrolase 2 and nitric oxide synthase expressions in Madin Darby Canine Kidney II cells.
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- Journal of Natural Medicines, 2013, v. 67, n. 4, p. 782, doi. 10.1007/s11418-013-0749-0
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Application of quantitative H-NMR method to determination of paeoniflorin in Paeoniae radix.
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- Journal of Natural Medicines, 2013, v. 67, n. 3, p. 657, doi. 10.1007/s11418-012-0711-6
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Application of H-NMR spectroscopy to validation of berberine alkaloid reagents and to chemical evaluation of Coptidis Rhizoma.
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- Journal of Natural Medicines, 2011, v. 65, n. 2, p. 262, doi. 10.1007/s11418-010-0490-x
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Quantitative determination of atractylon in Atractylodis Rhizoma and Atractylodis Lanceae Rhizoma by <sup>1</sup>H-NMR spectroscopy.
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- Journal of Natural Medicines, 2010, v. 64, n. 2, p. 161, doi. 10.1007/s11418-010-0393-x
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HPLC profiling of Phellinus linteus.
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- Journal of Natural Medicines, 2008, v. 62, n. 4, p. 441, doi. 10.1007/s11418-008-0260-1
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Tradescantia pallida extract inhibits biofilm formation in Pseudomonas aeruginosa.
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- Nagoya Journal of Medical Science, 2019, v. 81, n. 3, p. 439, doi. 10.18999/nagjms.81.3.439
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In situ UDP-glucose regeneration unravels diverse functions of plant secondary product glycosyltransferases
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- FEBS Letters, 2012, v. 586, n. 24, p. 4344, doi. 10.1016/j.febslet.2012.10.045
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UGT75L6 and UGT94E5 mediate sequential glucosylation of crocetin to crocin in Gardenia jasminoides
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- FEBS Letters, 2012, v. 586, n. 7, p. 1055, doi. 10.1016/j.febslet.2012.03.003
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Chemopreventive Action of Xanthone Derivatives on Photosensitized DNA Damage.
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- Photochemistry & Photobiology, 2005, v. 81, n. 2, p. 314, doi. 10.1111/j.1751-1097.2005.tb00189.x
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Studies on the chemical transformations of rotenoids. 5.
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- Journal of Heterocyclic Chemistry, 1998, v. 35, n. 3, p. 591, doi. 10.1002/jhet.5570350316
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Synthesis and central nervous system stimulant activity of camphor-1,2,4-benzotriazines fused with five and six-membered heterocycles.
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- Journal of Heterocyclic Chemistry, 1998, v. 35, n. 2, p. 293, doi. 10.1002/jhet.5570350205
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Synthesis and central nervous system stimulant activity of 5,8-methanoquinazolines fused with 1,2,4-triazole, tetrazoleand 1,2,4-triazine.
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- Journal of Heterocyclic Chemistry, 1998, v. 35, n. 2, p. 325, doi. 10.1002/jhet.5570350211
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Synthesis and central nervous system stimulant activity of 5,8-methanoquinazolines fused with imidazole, thiadiazole, pyrimidine and 1,3,5-triazine.
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- Journal of Heterocyclic Chemistry, 1998, v. 35, n. 2, p. 329, doi. 10.1002/jhet.5570350212
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Ring transformation of 5-amino (or acylamino)-6-hydroxy (or benzoyloxy)methylpyrimidin-4(3 H)-ones into 1 H-imidazoles.
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- Journal of Heterocyclic Chemistry, 1997, v. 34, n. 3, p. 761, doi. 10.1002/jhet.5570340310
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Antioxidant and Cytotoxic Effects of Moltkia aurea Boiss.
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- Records of Natural Products, 2012, v. 6, n. 1, p. 62
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Production of unnatural glucosides of curcumin with drastically enhanced water solubility by cell suspension cultures of Catharanthus roseus
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- FEBS Letters, 2003, v. 555, n. 2, p. 311, doi. 10.1016/S0014-5793(03)01265-1
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CYP98A6 from Lithospermum erythrorhizon encodes 4-coumaroyl-4′-hydroxyphenyllactic acid 3-hydroxylase involved in rosmarinic acid biosynthesis<sup>1</sup><FN ID="FN1"><NO>1</NO>The nucleotide sequence reported here will appear in the DDBJ/EMBL/GenBank Nucleotide Sequences Database under the accession number AB017418 (CYP98A6).</FN>
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- FEBS Letters, 2002, v. 514, n. 2/3, p. 219, doi. 10.1016/S0014-5793(02)02368-2
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Sasa veitchii extract protects against carbon tetrachloride-induced hepatic fibrosis in mice.
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- Environmental Health & Preventive Medicine, 2018, v. 23, n. 1, p. N.PAG, doi. 10.1186/s12199-018-0739-7
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Kampo formula 'Hochu-ekki-to' suppressed carbon tetrachloride-induced hepatotoxicity in mice.
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- Environmental Health & Preventive Medicine, 2016, v. 21, n. 6, p. 579, doi. 10.1007/s12199-016-0571-x
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Serotonin Derivative, N-(p-Coumaroyl)serotonin, Isolated from Safflower (Carthamus tinctorius L.) Oil Cake Augments the Proliferation of Normal Human and Mouse Fibroblasts in Synergy with Basic Fibroblast Growth Factor (bFGF) or Epidermal Growth ...
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- Journal of Biochemistry, 1999, v. 125, n. 5, p. 910, doi. 10.1093/oxfordjournals.jbchem.a022368
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