about
Partial resistance of carrot to Alternaria dauci correlates with in vitro cultured carrot cell resistance to fungal exudatesSelective detection of alkaloids in MALDI-TOF: the introduction of a novel matrix molecule.Semisynthetic and Natural Garcinoic Acid Isoforms as New mPGES-1 Inhibitors.New cytotoxic guttiferone analogues from Garcinia virgata from New Caledonia.Semisynthesis of alpha-methyl-gamma-lactones and in vitro evaluation of their activity on protein farnesyltransferase.Studies on the reactivity of a tertiary allylic alcohol in an acetophenonic series, a model for natural products synthesis.Tuning a 96-well microtiter plate fluorescence-based assay to identify AGE inhibitors in crude plant extracts.New and antifungal xanthones from Calophyllum caledonicum.First 2-hydroxy-3-methylbut-3-enyl substituted xanthones isolated from plants: structure elucidation, synthesis and antifungal activity.Front face fluorescence spectroscopy and visible spectroscopy coupled with chemometrics have the potential to characterise ripening of Cabernet Franc grapes.Advanced glycation inhibition and protection against endothelial dysfunction induced by coumarins and procyanidins from Mammea neurophylla.Bithiophenic MALDI matrices as valuable leads for the selective detection of alkaloids.Synthesis and biological activity of fluorescent neonicotinoid insecticide thiamethoxam.Multi-grams scale purification of xanthanolides from Xanthium macrocarpum. Centrifugal partition chromatography versus silica gel chromatography.Senecipyrrolidine, an unusual pyrrolidine alkaloid isolated from Jacobaea gigantea (Desf.) Pelser (Asteraceae)Endogenous metabolites of vitamin E limit inflammation by targeting 5-lipoxygenaseNew xanthones from Calophyllum caledonicumNovel cytotoxic 4-phenylfuranocoumarins from Calophyllum disparCytotoxic coumarins from Calophyllum disparSyntheses of Strychnos and Aspidospermatan-Type Alkaloids. 8. Selective Total Syntheses of Mossambine and 14-epi-Mossambine by a Radical Cyclization Reaction(1)Three 1-thio-beta-D-glucopyranosides from the seeds of Afrostyrax lepidophyllus MildbrIdentification of Minor Benzoylated 4-Phenylcoumarins from a Mammea neurophylla Bark ExtractFluorescent self-assembled monolayers of umbelliferone: a relationship between contact angle and fluorescenceSynthesis and evaluation of naphthoic acid derivatives as fluorescent probes to screen advanced glycation end-products breakersTwo new triterpenoid saponins from the leaves of Bupleurum lancifolium (Apiaceae)Efficient Semi-Synthesis of Natural δ-( R)-Tocotrienols from a Renewable Vegetal SourceSynthesis and antifungal activity of new thienyl and aryl conazolesSynthesis of new isoxazoles and dihydroisoxazoles and in vitro evaluation of their antifungal activitySynthesis of new 1-[2-Azido-2-(2,4-dichlorophenyl)ethyl]-1H/-imidazoles and in vitro evaluation of their antifungal activity
P50
Q28540220-B2FB645A-1370-4E61-A18A-A62FF8769E9BQ34242683-D3DB294C-EEB3-49EF-9DE1-5D7A13DCA773Q38765274-FCCD2BA8-5347-467F-BB64-E0A419099564Q40322430-F018A9B2-CC88-4B42-B922-CC490D51702BQ43133526-84AEDC25-54BD-4E54-87D6-E5DBC01FED40Q43692548-BED87C9E-7408-41C3-AFD1-FCE659D0CC08Q43743450-2A4F265B-9DDE-46AD-862F-442971706846Q43884546-760EEE59-2820-455B-8B25-F7B152FA4C90Q44434157-ED1D1EB1-9DF6-452D-BBF2-B7C16B06BD44Q46523658-EE16E2C8-87A8-41BD-A753-74AE4CEAF291Q46905750-EDF19D3B-11BE-4A96-99B9-3811285240BDQ49631993-2E6FB3EB-0DB8-495F-A4E7-AE8F3476D217Q52774124-63576B5A-E7CE-43B6-8293-67ACFB4E7586Q55043738-B5485DAD-CEC0-4C3F-974A-9426825389A2Q58097771-82A403BA-6DE6-42B0-99EF-A64F0B88EE05Q58712093-4986E1A3-4BDD-4C92-BC68-0527BB3B630CQ73213388-940E0132-9AAB-4E59-9A0F-9C4E1EBCD2DBQ73931738-DF94687E-615E-4E73-A5BF-DC418DBAF193Q74567460-92658DF7-A096-4EE5-8A3F-CFF75E57DA09Q74824683-780F055F-2FAE-4217-8817-6C7EC3A66617Q79283102-34A43ABC-B8E1-4ACA-A77F-0BDED9DC8B9BQ86256218-8E189333-EBE8-41E5-BD63-C074F5A2226CQ87137216-0FEE07A9-0C58-4594-9765-509300BA2C53Q87375375-AAF02DD5-1DD3-4E41-B8A2-D84C10E971AEQ88005124-3738DC69-46A2-4A67-92B0-5498469AC761Q90982247-6D1A3400-DFCA-44FC-BD79-163F4A6E4305Q94487910-DA05F82C-4EBA-4929-9E51-B5C02032409DQ94608255-B0813639-6BF6-49CE-A746-0519CF5BBB6BQ94706868-88F9D32A-2B75-4E35-B02A-21C3E64E21E3
P50
description
researcher ORCID ID = 0000-0002-0509-5788
@en
name
Denis Séraphin
@ast
Denis Séraphin
@en
Denis Séraphin
@nl
type
label
Denis Séraphin
@ast
Denis Séraphin
@en
Denis Séraphin
@nl
prefLabel
Denis Séraphin
@ast
Denis Séraphin
@en
Denis Séraphin
@nl
P31
P496
0000-0002-0509-5788