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Selection of Reference Genes for Gene Expression Normalization in Peucedanum praeruptorum Dunn under Abiotic Stresses, Hormone Treatments and Different Tissues.Integration of a Decrescent Transcriptome and Metabolomics Dataset of Peucedanum praeruptorum to Investigate the CYP450 and MDR Genes Involved in Coumarins Biosynthesis and TransportCytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis.Cloning, Functional Characterization, and Catalytic Mechanism of a Bergaptol O-Methyltransferase from Peucedanum praeruptorum DunnCloning, Functional Characterization and Site-Directed Mutagenesis of 4-Coumarate: Coenzyme A Ligase (4CL) Involved in Coumarin Biosynthesis in Peucedanum praeruptorum Dunn.Identification and functional characterization of a p-coumaroyl CoA 2'-hydroxylase involved in the biosynthesis of coumarin skeleton from Peucedanum praeruptorum Dunn.Cytotoxic withanolides from Physalis angulata.Trichiconlides A and B: two novel limonoids from the fruits of Trichilia connaroides.Further C-15-acyl phragmalin derivatives from Chukrasia tabularis A. Juss.Limonoids from the stem bark of Khaya senegalensis.A new acorane sesquiterpene from the aerial parts of Psychotria yunnanensis.New cassane-type diterpenoids from Caesalpinia bonduc.Chemical constituents from Trichilia connaroides and their nitric oxide production and α-glucosidase inhibitory activities.Inhibitory effect of four triterpenoids from trichilia connaroides on nitric oxide production in lipopolysaccharide-stimulated RAW264.7 cells.The Anti-inflammatory Activities of Two Major Withanolides from Physalis minima Via Acting on NF-κB, STAT3, and HO-1 in LPS-Stimulated RAW264.7 Cells.Sesquiterpenes from the aerial part of Chloranthus japonicus and their cytotoxicities.Three new phenolic glucosides from the roots of Rheum palmatum.Polyprenylated Tetraoxygenated Xanthones from the Roots of Hypericum monogynum and Their Neuroprotective Activities.Sarglaperoxides A and B, Sesquiterpene-Normonoterpene Conjugates with a Peroxide Bridge from the Seeds of Sarcandra glabra.Hypermongones A-J, Rare Methylated Polycyclic Polyprenylated Acylphloroglucinols from the Flowers of Hypericum monogynum.New indole glucosides as biosynthetic intermediates of camptothecin from the fruits of Camptotheca acuminata.Monoterpene indole alkaloids from the stem bark of Mitragyna diversifolia and their acetylcholine esterase inhibitory effects.Two new C-15 enolic acyl phragmalin-type limonoids from Chukrasia tabularis var. velutina.Identification and analysis of gastrodin and its five metabolites using ultra fast liquid chromatography electrospray ionization tandem mass spectrometry to investigate influence of multiple-dose and food.Cassane-type diterpenoids from the seed kernels of Caesalpinia bonduc.Trichiconlides CF, four new limonoids with 1,2-seco phragmalin-type carbon skeleton from the fruits of Trichilia connaroides.Two new polyhydroxyl polyacetylenes from fruits of Herpetospermum caudigerum.New triterpenoids with diverse side-chains from the barks of Melia Toosendan.One-step targeted accumulation and detection of camptothecin analogues from fruits of Camptotheca acuminata Decne using bilayer solid-phase extraction coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry.Near-Infrared Fluorescent Probe with Remarkable Large Stokes Shift and Favorable Water Solubility for Real-Time Tracking Leucine Aminopeptidase in Living Cells and In Vivo.Antimicrobial metabolites from the plant endophytic fungus Penicillium sp.Hydrogen/deuterium exchange, a unique and effective method for MS fragmentation behavior elucidation of ginkgolides and its application to systematic research in Ginkgo biloba.Sophoraflavanone G from Sophora alopecuroides inhibits lipopolysaccharide-induced inflammation in RAW264.7 cells by targeting PI3K/Akt, JAK/STAT and Nrf2/HO-1 pathways.Anti-inflammatory activity of Khayandirobilide A from Khaya senegalensis via NF-κB, AP-1 and p38 MAPK/Nrf2/HO-1 signaling pathways in lipopolysaccharide-stimulated RAW 264.7 and BV-2 cells.Analysis and pharmacokinetics studies of gastrodin and p-hydroxybenzyl alcohol in dogs using ultra fast liquid chromatography-tandem mass spectrometry method.Diverse tritepenoids from the fruits of Walsura robusta and their reversal of multidrug resistance phenotype in human breast cancer cells.New Structurally Diverse Limonoids from the Seeds of Khaya senegalensis.Novel tirucallane-type triterpenoids from Aphanamixis grandifoliaNovel nortriterpenoids from Aphanamixis grandifoliaAnti-inflammatory sesquiterpenes and sesquiterpene dimers from Chloranthus fortunei
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Q35972516-6A36F520-6734-4036-B4D3-AA743C65F02EQ36360290-C7C3E645-428C-4C34-916F-FAC0B4675D22Q36512335-E4B8A3A8-E81C-4DE9-9762-934685A929F2Q36933227-34D30AE2-D650-4D38-B8EF-7490AE5A8C51Q37588611-97D71E43-E621-4158-9580-696F821A870EQ38617826-7D8B08BF-700F-4173-827D-9B876EACEF86Q38700296-57DE4C33-6362-4163-BDD0-73AA737A9B63Q38811109-D02ABF93-3103-4AA6-929B-2287B4E66574Q38851834-C140A3D6-602E-48D6-8BBB-2413D6236580Q38891908-90734CEA-4937-4E5C-A5D7-6FEED0650163Q38976747-E03312FE-42D4-4CA2-B8E2-C91FFF5B27EDQ38978562-CC2ED4F1-D3EB-4B32-A07C-A406F790D601Q39041668-B753F9EB-49D2-4C4A-AA7D-3CBE82A6E082Q39088686-F7B19385-FEB2-417F-8C5F-CEBD562CF581Q39134389-93702F75-F3D7-4CD5-A611-614D542636D5Q39276916-69AE2A03-9B7A-4533-82DC-3E14176ECDEAQ39403614-8CF2E93D-9531-4C35-877E-C77E68E8E1FBQ39489781-817EA9A7-8E80-47C1-A2D8-068021607BCAQ40043806-72A68846-E919-4CE4-963C-6ECE80EB3591Q40998884-2BBCEEAD-8DE9-465C-B3DC-DA6770482E37Q41223302-A115C010-8316-4CE0-905A-16FB5B471D67Q45081326-A1121DF6-AF61-4AD1-865C-18AB4522CD65Q45188777-637435C6-D1C4-46E5-98B0-569A2520676BQ46732460-6B953A21-16E9-486A-8ABD-D2B54715C3EEQ46805211-B8659FA2-2A85-45B0-AA70-9680AC2FCA27Q47210865-B9623D98-48D8-4ECC-89F4-61A126DB7279Q47224378-64D3B150-576B-4F4E-8B0D-7FC8DFD0B54EQ47802828-75114E4D-A36A-48B5-BB06-509982439D0CQ47833904-0D932B75-98BE-471F-A821-84018D7D54E7Q47835915-45FAF753-4F61-46E2-9E42-7F8ADB6B48D6Q47849591-C5669402-FD1A-4373-961D-A771AD4DAEB3Q48913719-FE869DEA-DDF0-4D8D-8674-A448A008B46EQ51676903-77704A57-6FFA-4DFD-9AB6-4BF50FC30548Q52588260-43A0DFFF-CC10-45D0-9D3E-97690ED95C30Q53477366-FF414A03-B0E6-4136-B680-185D088841E5Q53752513-6050ACE9-A020-45F2-B4E4-5C3A73D2CD44Q53815475-C39D3F58-7EC7-4B48-AE31-C0380F7A6FB1Q82506878-E75BAA8E-7C5B-496B-A01D-9353C25306D9Q83378825-50004CA2-6557-4645-85A2-321F570F35AAQ84102858-65F529A7-FDC5-43B4-886E-EEBBBAAD47EF
P50
description
researcher ORCID: 0000-0002-7892-011X
@en
name
Jun Luo
@ast
Jun Luo
@en
Jun Luo
@es
Jun Luo
@nl
type
label
Jun Luo
@ast
Jun Luo
@en
Jun Luo
@es
Jun Luo
@nl
prefLabel
Jun Luo
@ast
Jun Luo
@en
Jun Luo
@es
Jun Luo
@nl
P106
P1153
35867345600
P31
P496
0000-0002-7892-011X