about
Molecular cloning, functional expression and characterization of d-limonene synthase from Schizonepeta tenuifoliaIsolation and structure elucidation of gymnemic acids, antisweet principles of Gymnema sylvestre.Tropane alkaloid production and shoot regeneration in hairy and adventitious root cultures of Duboisia myoporoides-D. leichhardtii hybrid.A review on phytochemistry and medicinal properties of the genus Achillea.Synthesis, inhibitory effects on nitric oxide and structure-activity relationships of a glycosphingolipid from the marine sponge Aplysinella rhax and its analogues.Antichagasic activity of komaroviquinone is due to generation of reactive oxygen species catalyzed by Trypanosoma cruzi old yellow enzyme.Two new sulfated oleanan saponins from Achyranthes root.Genetic and Phenotypic Analyses of a Papaver somniferum T-DNA Insertional Mutant with Altered Alkaloid Composition.Synthesis, antigenicity against human sera and structure-activity relationships of carbohydrate moieties from Toxocara larvae and their analogues.Application of a new method, orthogonal projection to latent structure (OPLS) combined with principal component analysis (PCA), to screening of prostaglandin E2 production inhibitory flavonoids in Scutellaria Root.Two new lignans and melanogenesis inhibitors from Schisandra nigra.Scillapersicene: a new homoisoflavonoid with cytotoxic activity from the bulbs of Scilla persica HAUSSKN.Biochemical and biophysical properties of a novel homoisoflavonoid extracted from Scilla persica HAUSSKN.Sulfatides inhibit adhesion, migration, and invasion of murine melanoma B16F10 cell line in vitro.Anticarcinogenic compounds in the Uzbek medicinal plant, Helichrysum maracandicum.Synthesis and Antigenicity against Human Sera of a Biotin-Labeled Oligosaccharide Portion of a Glycosphingolipid from the Parasite Echinococcus multilocularis.An unusual sesquiterpene derivative from Ferula kuhistanica.Galα1-4Galβ1-3GalNAc is the dominant epitope of Em2 antigen, the mucin-type glycoprotein from Echinococcus multilocularis.Synthesis of the carbohydrate moiety from the parasite Echinococcus multilocularis and their antigenicity against human sera.Genetic and chemical comparison of Boi (Sinomeni Caulis et Rhizoma) and Seifuto (Caulis Sinomenii).Monoterpene hydroperoxides with trypanocidal activity from Chenopodium ambrosioides.Trypanocidal terpenoids from Laurus nobilis L.Transformation of ipecac (Cephaelis ipecacuanha) with Agrobacterium rhizogenes.Advanced method for assignment of absolute configuration utilizing an induced CD and computational technique: its application to natural products possessing a secondary alcohol.New norditerpenoids with trypanocidal activity from Vitex trifolia.Bioactive constituents from Dracocephalum subcapitatum (O. Kuntze) Lipsky.A guanidine derivative from seeds of Plantago asiatica.Growth characteristics of Cannabis sativa L. cultivated in a phytotron and in the field.A new phenolic glucoside from an Uzbek medicinal plant, Origanum tyttanthum.A rapid and reliable solid-phase extraction method for high-performance liquid chromatographic analysis of opium alkaloids from papaver plants.Evaluation of the taste of crude drug and Kampo formula by a taste-sensing system (4): taste of Processed Aconite Root.Nepetaefuran and leonotinin isolated from Leonotis nepetaefolia R. Br. potently inhibit the LPS signaling pathway by suppressing the transactivation of NF-κB.Synergistic effect of baicalein, wogonin and oroxylin A mixture: multistep inhibition of the NF-κB signalling pathway contributes to an anti-inflammatory effect of Scutellaria root flavonoids.Synthesis and biological evaluation of the natural product komaroviquinone and related compounds aiming at a potential therapeutic lead compound for high-risk multiple myeloma.Inhibitory effects of flavonoids extracted from Nepalese propolis on the LPS signaling pathway.Three new 5,6,7,8-tetrahydroxy-5,6,7,8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood.Improvement of benzylisoquinoline alkaloid productivity by overexpression of 3'-hydroxy-N-methylcoclaurine 4'-O-methyltransferase in transgenic Coptis japonica plants.New icetexane and 20 norabietane diterpenes with trypanocidal activity from Dracocephalum komaroviParadisin C: a new CYP3A4 inhibitor from grapefruit juiceNematocidal activity of long alkyl chain amides, amines, and their derivatives on dog roundworm larvae
P50
Q28212756-266D6465-E114-4BE3-ACC1-B633DD241125Q30832219-2DF19CE0-2F8F-4283-B42B-E9A84F0E62F7Q33340298-8A642BD6-2143-4AD1-ABD2-A1EFCD13E201Q33454598-09B8D0DA-0A77-471E-91E5-05126023D380Q33795728-9E0DA819-39B6-4648-82A9-414740EC42BDQ34228338-89C41BA7-9E6E-4765-A683-8CDA7171CB54Q34330408-57F9B3CF-54BD-4914-9A1F-C862820A2E29Q37148695-1E0A8921-2DF8-45FF-99B0-87E46F1CE060Q38323059-D7308189-821D-4ADC-8FF4-B0DFCF9B0A07Q38771938-9C2686D4-2261-41B4-A1E8-C8C36641D750Q38773443-E8BBF2C9-76ED-4C98-AAED-FDDFEAFE3897Q38856971-46AA0BD3-ACB1-43A5-891D-C5B5593B5293Q38960442-30BE9381-CE30-4AFD-A517-A0F363475B81Q39280105-C8E98F76-D0AB-46C5-A13B-A924ADE4F07FQ39992997-1A5F0516-CBA0-4395-80E6-31ECB89EF5C5Q40627044-6118376D-8600-409D-B9F0-E0DCFCD87C2BQ40701235-9E909409-B12C-49C6-9EF7-985B34FE49AEQ42719592-22274658-FE88-4A19-AA07-FD6F715FB45EQ42746077-E1D2ED18-6CD5-4918-88CF-3A614905ACDDQ43136167-2CA12320-7AF3-4560-A326-8A71013895EBQ43970571-06C35B04-601B-4906-9FAA-74F79564DCD7Q44207822-8FC12B8D-514B-4415-8FB7-24CE5AD76B7EQ44736369-A01DF061-DC72-4C64-A442-653A2F5D4D31Q45074799-D5104B42-B6F5-420D-8B27-22299EC83E85Q45172030-78733559-B510-4166-93CE-C9057E55719DQ46400427-563CF2B2-E2EA-4D21-BE00-BE65338D857BQ46456534-AB9B70A9-DE9D-4645-A291-ECAA7FFB9710Q46532176-7E8525BE-396D-4014-A076-B15D0D0A114CQ46651059-8DCA6015-1D18-4F01-95E0-8A0E0C30E3A0Q46792827-7A121A2A-7C3E-4307-BBB5-00965D22C944Q47336209-6336B267-3584-4534-8D13-6BB71DC00AC4Q47383430-2AF91040-02F6-47AF-9850-230BC2EF0D77Q47787057-7940565F-504E-4435-9C23-A48C2E369D5DQ48018647-7E80D463-46A7-4D8D-A2F6-8677DB4CC629Q51369476-34B7A7CB-C197-4726-8A81-2182DAC8FD9BQ52662420-C64304E1-9050-4EEC-ACF2-D4F3896F28BBQ54305656-4200E27B-4C6A-4ECE-A079-503AEAA945F2Q58846078-0A7809BE-FDB1-450A-9732-B05CB192972AQ59710795-312BA3CC-488F-4727-9364-481CFD09930CQ67477773-F5E20D7C-8B71-4558-B086-49D87BBFF190
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fumiyuki Kiuchi
@ast
Fumiyuki Kiuchi
@en
Fumiyuki Kiuchi
@es
Fumiyuki Kiuchi
@nl
type
label
Fumiyuki Kiuchi
@ast
Fumiyuki Kiuchi
@en
Fumiyuki Kiuchi
@es
Fumiyuki Kiuchi
@nl
prefLabel
Fumiyuki Kiuchi
@ast
Fumiyuki Kiuchi
@en
Fumiyuki Kiuchi
@es
Fumiyuki Kiuchi
@nl
P106
P108
P31
P496
0000-0002-9338-5047