About: Mehdi A Beniddir

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0003-2153-4290

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) personne médaillée du CNRS (fr) researcher ORCID ID = 0000-0003-2153-4290 (en)
rdfs:label	Mehdi A Beniddir (en) Mehdi A Beniddir (es) Mehdi A Beniddir (nl) Mehdi A Beniddir (ast) Mehdi Beniddir (de) Mehdi Beniddir (fr)
skos:prefLabel	Mehdi A Beniddir (en) Mehdi A Beniddir (es) Mehdi A Beniddir (nl) Mehdi A Beniddir (ast) Mehdi Beniddir (de) Mehdi Beniddir (fr)
name	Mehdi A Beniddir (en) Mehdi A Beniddir (es) Mehdi A Beniddir (nl) Mehdi A Beniddir (ast) Mehdi Beniddir (de) Mehdi Beniddir (fr)
Scopus author ID	wds:Q57858606-505E7373-A501-458A-9CAE-C212CCC83545
Scopus author ID	36087002000
instance of	wds:Q57858606-08AF1185-BC35-40ED-A558-7E6C165B5F99
described at URL	wds:Q57858606-85DC36D5-488F-42BA-92DD-1CE11B366F9E
instance of	Homo sapiens
described at URL	https://www.cnrs.fr/fr/personne/mehdi-beniddir
award received	wds:Q57858606-49DDE5FF-6349-4F22-B48F-EB65840177B0
award received	CNRS bronze medal
skos:altLabel	Mehdi Beniddir (en)
occupation	wds:Q57858606-04989ADF-4CC4-41FD-AC95-CF1DB643E97C
employer	wds:Q57858606-9B4B9AF1-68CC-436A-A436-0857F7470B05
sex or gender	wds:Q57858606-7787b94a-8370-4f35-a8a9-fe398b3e319c
ISNI	wds:Q57858606-D51397AE-4326-47E3-8B00-ECD8AD316DB9
VIAF ID	wds:Q57858606-380A9667-F798-4E51-951F-3013719795C1
IdRef ID	wds:Q57858606-33E8A304-0A7C-4C26-8716-758F82B413E1
date of birth	wds:Q57858606-B9DE9DA6-2DD1-409A-A195-04D33F08FD24
VIAF ID	http://viaf.org/viaf/296151867
IdRef ID	http://www.idref.fr/166300535/id
occupation	researcher
employer	University of Paris-Sud
sex or gender	male
ISNI	0000000401710434
VIAF ID	296151867
IdRef ID	166300535
date of birth	1985-01-01 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q57858606-CE7D6676-5A23-499D-8271-F9517A8675FD
ORCID iD	https://orcid.org/0000-0003-2153-4290
ORCID iD	0000-0003-2153-4290
CNRS Talent page	wds:Q57858606-4D6D993C-CD40-4B15-9F7B-0B727084AAC2
CNRS Talent page	mehdi-beniddir
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57858606
is author of	Acridone alkaloids from Glycosmis chlorosperma as DYRK1A inhibitors DNA-Templated [2+2] Photocycloaddition: A Straightforward Entry into the Aplysinopsin Family of Natural Products Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings. Revisiting Previously Investigated Plants: A Molecular Networking-Based Study of Geissospermum laeve. The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research Sanctis A-C: Three Racemic Procyanidin Analogues from The Lichen Parmotrema sancti-angelii DP4-Assisted Structure Elucidation of Isodemethylchodatin, a New Norlichexanthone Derivative Meager in H-Atoms, from the Lichen Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum Collected mass spectrometry data on monoterpene indole alkaloids from natural product chemistry research CANPA: Computer-Assisted Natural Products Anticipation Natural products targeting strategies involving molecular networking: different manners, one goal Pleiokomenines A and B: Dimeric Aspidofractinine Alkaloids Tethered with a Methylene Group. Theionbrunonines A and B: Dimeric Vobasine Alkaloids Tethered by a Thioether Bridge from Mostuea brunonis Goniomedines A and B: unprecedented bisindole alkaloids formed through fusion of two indole moieties via a dihydropyran unit Molecular Networking Reveals Serpentinine-Related Bisindole Alkaloids from Picralima nitida, a Previously Well-Investigated Species Corynanthean-Epicatechin Flavoalkaloids from Corynanthe pachyceras Phenylpropane as an Alternative Dearomatizing Unit of Indoles: Discovery of Inaequalisines A and B Using Substructure-Informed Molecular Networking A database of high-resolution MS/MS spectra for lichen metabolites Targeted Isolation of Hemitheion from Mostuea brunonis, a Proposed Biosynthetic Intermediate of Theionbrunonines Metabolomics-Driven Discovery of Meroterpenoids from a Mussel-Derived Penicillium ubiquetum From the Spectroscopic Reassessment of Authentic Alkaloid Samples to the Molecular Networking-Guided Discovery of Criophylline-Related Analogues from Callichilia inaequalis Voatriafricanines A and B, Trimeric Vobasine-Aspidosperma-Aspidosperma Alkaloids from Voacanga africana Turrianes from Kermadecia rotundifolia as new acetylcholinesterase inhibitors Advances in decomposing complex metabolite mixtures using substructure- and network-based computational metabolomics approaches Bisindole alkaloid artifacts from Gonioma malagasy Resolving the (19 R) Absolute Configuration of Lanciferine, a Monoterpene Indole Alkaloid from Alstonia boulindaensis An Unprecedented Blue Chromophore Found in Nature using a "Chemistry First" and Molecular Networking Approach: Discovery of Dactylocyanines A-H. A unified bioinspired "aplysinopsin cascade": total synthesis of (±)-tubastrindole B and related biosynthetic congeners. Spontaneous biomimetic formation of (±)-dictazole B under irradiation with artificial sunlight Antiplasmodial Securinega alkaloids from Phyllanthus fraternus : Discovery of natural (+)-allonorsecurinine Nervisides I-J: Unconventional Side-Chain-Bearing Cycloartane Glycosides from Nervilia concolor Five new cassane diterpenes from the seeds and bark of Erythrophleum suaveolens New Benthic Cyanobacteria from Guadeloupe Mangroves as Producers of Antimicrobials Solid-Phase Extraction Embedded Dialysis (SPEED), an Innovative Procedure for the Investigation of Microbial Specialized Metabolites A Reappraisal of the Structure of Lyaline as the First Naturally Occurring Nacycline Monoterpene Indole Alkaloid Pyrrovobasine, hybrid alkylated pyrraline monoterpene indole alkaloid pseudodimer discovered using a combination of mass spectral and NMR-based machine learning annotations Structure elucidation of an aspidofractinine-type monoterpene indole alkaloid from Melodinus reticulatus Diarylheptanoid Glucosides from Pyrostria major and Their Antiprotozoal Activities Antiplasmodial activity of selected medicinal plants used to treat malaria in Ghana

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