Grégory Genta-Jouve

Dr. Grégory Genta-Jouve

USR 3456 CNRS LEEISA
+1
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 September 2017 in ACS Chemical Biology
Verified
Journal Article
Open access
FOFlorent Olivon
Florent Olivon
PAPierre-Marie Allard
Pierre-Marie Allard
AKAlexey Koval
Alexey Koval
DRDavide Righi
Davide Righi
Grégory Genta-JouveGrégory Genta-Jouve
Grégory Genta-Jouve
Marc LitaudonMarc Litaudon
Marc Litaudon
Natural products represent an inexhaustible source of novel therapeutic agents. Their complex and constrained three-dimensional structures endow these molecules with exceptional biological properties, thereby giving them a major role in drug discovery programs. However, the search for new bioactive metabolites is hampered by the chemical complexity of the biological matrices in which they are found. The purification of single constituents from such matrices requires such a significant amount of work that it should be ideally performed only on molecules of high potential value (i.e., chemical novelty and biological activity). Recent bioinformatics approaches based on mass spectrometry metabolite profiling methods are beginning to address the complex task of compound identification within complex mixtures. However, in parallel to these developments, methods providing information on the bioactivity potential of natural products prior to their isolation are still lacking and are of key interest to target the isolation of valuable natural products only. In the present investigation, we propose an integrated analysis strategy for bioactive natural products prioritization. Our approach uses massive molecular networks embedding various informational layers (bioactivity and taxonomical data) to highlight potentially bioactive scaffolds within the chemical diversity of crude extracts collections. We exemplify this workflow by targeting the isolation of predicted active and nonactive metabolites from two botanical sources (Bocquillonia nervosa and Neoguillauminia cleopatra) against two biological targets (Wnt signaling pathway and chikungunya virus replication). Eventually, the detection and isolation processes of a daphnane diterpene orthoester and four 12-deoxyphorbols inhibiting the Wnt signaling pathway and exhibiting potent antiviral activities against the CHIKV virus are detailed. Combined with efficient metabolite annotation tools, this bioactive natural products prioritization pipeline proves to be efficient. Implementation of this approach in drug discovery programs based on natural extract screening should speed up and rationalize the isolation of bioactive natural products.

18 June 2021 in Natural Product Reports
Verified
Journal Article
Open access
PDF file
MBMehdi Beniddir
Mehdi Beniddir
KKKyo Bin Kang
Kyo Bin Kang
Grégory Genta-JouveGrégory Genta-Jouve
Grégory Genta-Jouve
FHFlorian Huber
Florian Huber
SRSimon Rogers
Simon Rogers
Justin Van der HooftJustin Van der Hooft
Justin Van der Hooft
This review highlights the key computational tools and emerging strategies for metabolite annotation, and discusses how these advances will enable integrated large-scale analysis to accelerate natural product discovery.

1 February 2017 in Current Opinion in Chemical Biology
Verified
Journal Article
Closed access
PAPierre-marie Allard
Pierre-marie Allard
Grégory Genta-JouveGrégory Genta-Jouve
Grégory Genta-Jouve
JWJean-Luc Wolfender
Jean-Luc Wolfender

13 July 2018 in Natural Product Reports
Verified
Journal Article
Open access
PDF file
JMJames B. McAlpine
James B. McAlpine
SCShao-Nong Chen
Shao-Nong Chen
AKAndrei G. Kutateladze
Andrei G. Kutateladze
JMJohn B MacMillan
John B MacMillan
Giovanni AppendinoGiovanni Appendino
Giovanni Appendino
GPGuido F. Pauli
Guido F. Pauli
With contributions from the global natural product (NP) research community, and continuing the Raw Data Initiative, this review collects a comprehensive demonstration of the immense scientific value of disseminating raw nuclear magnetic resonance (NMR) data, independently of, and in parallel with, classical publishing outlets.

5 January 2016 in Scientific Reports
Verified
Journal Article
Open access
PDF file
Christophe VieiraChristophe Vieira
Christophe Vieira
Olivier ThomasOlivier Thomas
Olivier Thomas
Gérald CulioliGérald Culioli
Gérald Culioli
Grégory Genta-JouveGrégory Genta-Jouve
Grégory Genta-Jouve
FHFanny Houlbreque
Fanny Houlbreque
CPClaude E. PAYRI
Claude E. PAYRI
Allelopathy has been recently suggested as a mechanism by which macroalgae may outcompete corals in damaged reefs. Members of the brown algal genus Lobophora are commonly observed in close contact with scleractinian corals and have been considered responsible for negative effects of macroalgae to scleractinian corals. Recent field assays have suggested the potential role of chemical mediators in this interaction. We performed in situ bioassays testing the allelopathy of crude extracts and isolated compounds of several Lobophora species, naturally associated or not with corals, against four corals in New Caledonia. Our results showed that, regardless of their natural association with corals, organic extracts from species of the genus Lobophora are intrinsically capable of bleaching some coral species upon direct contact. Additionally, three new C21 polyunsaturated alcohols named lobophorenols A–C (1–3) were isolated and identified. Significant allelopathic effects against Acropora muricata were identified for these compounds. In situ observations in New Caledonia, however, indicated that while allelopathic interactions are likely to occur at the macroalgal-coral interface, Lobophora spp. rarely bleached their coral hosts. These findings are important toward our understanding of the importance of allelopathy versus other processes such as herbivory in the interaction between macroalgae and corals in reef ecosystems.

26 August 2009 in Journal of Natural Products
Verified
Journal Article
Closed access
NCNadja Cachet
Nadja Cachet
Grégory Genta-JouveGrégory Genta-Jouve
Grégory Genta-Jouve
ERErik L. Regalado
Erik L. Regalado
RMRedouane Mokrini
Redouane Mokrini
PAPhilippe Amade
Philippe Amade
Olivier ThomasOlivier Thomas
Olivier Thomas