about
Integration of Microfractionation, qNMR and zebrafish screening for the in vivo bioassay-guided isolation and quantitative bioactivity analysis of natural productsSemisynthetic neoboutomellerone derivatives as ubiquitin-proteasome pathway inhibitors.Occurrence of the synthetic analgesic tramadol in an African medicinal plant.Dichapetalins from Dichapetalum species and their cytotoxic properties.Anti-inflammatory, antimicrobial and antioxidant activities of Diospyros bipindensis (Gürke) extracts and its main constituents.Peltogynoids and 2-phenoxychromones from Peltophorum pterocarpum and evaluation of their estrogenic activity.Meroterpenes from Dichrostachys cinerea inhibit protein farnesyl transferase activity.Vitis vinifera canes, a new source of antifungal compounds against Plasmopara viticola, Erysiphe necator, and Botrytis cinerea.Monoamine oxidase inhibition by monoterpene indole alkaloids and fractions obtained from Psychotria suterella and Psychotria laciniata.Proteasome inhibitors from Neoboutonia melleri.Protoflavonoids from ferns impair centrosomal integrity of tumor cells.Comprehensive profiling and marker identification in non-volatile citrus oil residues by mass spectrometry and nuclear magnetic resonanceSalvia officinalis for Hot Flushes: Towards Determination of Mechanism of Activity and Active PrinciplesPolyketide Skeletons from the Marine Alga-Derived FungusConiothyrium cerealeGrahamines A–E, Cyclobutane-Centered Tropane Alkaloids from the Aerial Parts ofSchizanthus grahamiiImpact of C5-cytosine methylation on the solution structure of d(GAAAACGTTTTC)2. An NMR and molecular modelling investigationFourier and wavelet transform analysis, a tool for visualizing regular patterns in DNA sequencesConformational variation of the central CG site in d(ATGACGTCAT)2 and d(GAAAACGTTTTC)2. An NMR, molecular modelling and 3D-homology investigationDiterpenoids and triterpenoids from Euphorbia guyonianaIndole alkaloids of Psychotria as multifunctional cholinesterases and monoamine oxidases inhibitorsRutamarin: Efficient Liquid-Liquid Chromatographic Isolation from Ruta graveolens L. and Evaluation of Its In Vitro and In Silico MAO-B Inhibitory Activity
P50
Q28488352-F41B23DC-9ED9-4944-80D3-A2A24C420887Q34114106-75E25238-4836-46C3-96E9-EF1E6D30062AQ34369467-052D2B14-4E68-4708-AAA2-52023F653870Q39160459-F29E7AD8-B36B-4B9C-9816-3ED04044E944Q39207957-BB0315F4-4730-4E3E-AA0F-73474D7AB1A0Q39362099-95C56A79-31B2-4729-A7D6-F0A33CA697D0Q43275355-F67DC15B-7842-45AC-9161-5C2E0A8412C7Q43692165-C5CC8C59-0E48-447B-86A4-DC30E1BAC5E5Q46206304-05FACD59-36E1-477D-8B6B-E4B7904D116FQ48023323-F6DCA533-53C8-40AF-BEF3-3B12F4720DD6Q53295709-D6D50ECD-B82C-441F-AE8E-EFB026756A4CQ58856031-0949DE03-EEAA-4B56-A877-2633FF97D181Q58856041-0B654FF9-802B-4365-B276-B26B62DA628FQ58856044-A658E759-B64F-4363-8367-FAE9890D07F2Q58864990-3A136CC7-C0E7-4ED6-9E91-F858119B5C5BQ73076772-0232C6EC-3B4B-46E2-A1E8-01819F933880Q74316347-8F5F1590-7C00-4463-8765-3753204C7A1CQ77363192-63FC1FFC-B0FF-4CBA-83EA-9F16E5B71542Q79871518-5FC6014E-2350-4B74-B2C2-BA9C4112C25BQ85767361-145D7504-879F-4A2C-B51E-79AFE89B58A6Q96294787-571DF6A5-C011-49EF-99CC-DDD4FC0E20B5
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Laurence Marcourt
@ast
Laurence Marcourt
@en
Laurence Marcourt
@es
Laurence Marcourt
@nl
Laurence Marcourt
@sl
type
label
Laurence Marcourt
@ast
Laurence Marcourt
@en
Laurence Marcourt
@es
Laurence Marcourt
@nl
Laurence Marcourt
@sl
prefLabel
Laurence Marcourt
@ast
Laurence Marcourt
@en
Laurence Marcourt
@es
Laurence Marcourt
@nl
Laurence Marcourt
@sl
P1053
A-3411-2014
P106
P31
P3829
P496
0000-0002-9614-1099