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M. Maillard · SciRah

Researcher profile · Semantic Scholar

M. Maillard

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M. Maillard — researcher profile on SciRah

h-index: 13
Works: 29
Citations: 806

Most-cited papers

8‐(3‐Chlorostyryl)caffeine (CSC) is a selective A2‐adenosine antagonist in vitro and in vivo
K. Jacobson, O. Nikodijević, W. Padgett, C. Gallo-Rodriguez +2 more
1993FEBS Letters177 citations Open access
Semantic Scholar
Design, synthesis, and biological evaluation of potent and selective class IIa histone deacetylase (HDAC) inhibitors as a potential therapy for Huntington's disease.
R. Bürli, C. Luckhurst, O. Aziz, K. Matthews +26 more
2013Journal of Medicinal Chemistry147 citations Open access
Semantic Scholar
Design, synthesis, and crystal structure of hydroxyethyl secondary amine-based peptidomimetic inhibitors of human beta-secretase.
M. Maillard, R. K. Hom, Timothy E. Benson, Joseph B. Moon +14 more
2007Journal of Medicinal Chemistry105 citations Open access
Semantic Scholar
Structure activity relationships for derivatives of adenosine‐5′‐triphosphate as agonists at P2 purinoceptors: Heterogeneity within P2x and P2y subtypes
G. Burnstock, B. Fischer, Charles H. V. Hoyle, M. Maillard +6 more
1994Drug development research (Print)87 citations Open access
Semantic Scholar
Comparative studies on the affinities of ATP derivatives for P2X‐purinoceptors in rat urinary bladder
X. Bo, B. Fischer, M. Maillard, K. Jacobson +1 more
1994British Journal of Pharmacology61 citations Open access
Semantic Scholar
Evaluation of 5-(Trifluoromethyl)-1,2,4-oxadiazole-Based Class IIa HDAC Inhibitors for Huntington's Disease.
A. Stott, M. Maillard, V. Beaumont, David J. Allcock +19 more
2021ACS Medicinal Chemistry Letters40 citations Open access
Semantic Scholar
Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitor.
C. Luckhurst, O. Aziz, V. Beaumont, R. Bürli +14 more
2019Bioorganic & Medicinal Chemistry Letters40 citations
Semantic Scholar
Exploiting differences in caspase-2 and -3 S₂ subsites for selectivity: structure-based design, solid-phase synthesis and in vitro activity of novel substrate-based caspase-2 inhibitors.
M. Maillard, F. Brookfield, S. M. Courtney, F. Eustache +14 more
2011Bioorganic & Medicinal Chemistry35 citations Open access
Semantic Scholar
Synthesis of 3'-substituted-2',3'-dideoxynucleoside analogs as potential anti-aids drugs
M. Maillard, A. Faraj, F. Frappier, J. Florent +2 more
198930 citations
Semantic Scholar
Preparation and anti-HIV activity of N-3-substituted thymidine nucleoside analogs.
D. Adams, C. Perez, M. Maillard, J. Florent +6 more
1997Journal of Medicinal Chemistry20 citations Open access
Semantic Scholar
Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: prime side chromane-containing inhibitors.
Raymond A. Ng, Minghua Sun, S. Bowers, R. K. Hom +22 more
2012Bioorganic & Medicinal Chemistry Letters14 citations Open access
Semantic Scholar
A new apo-caspase-6 crystal form reveals the active conformation of the apoenzyme.
I. Müller, M. Lamers, A. Ritchie, Hyunsun Park +4 more
2011Journal of Molecular Biology14 citations
Semantic Scholar
Identification of a Potent, Selective, and Brain-Penetrant Rho Kinase Inhibitor and its Activity in a Mouse Model of Huntington's Disease.
T. Ladduwahetty, Matthew R. Lee, M. Maillard, R. Cachope +21 more
2022Journal of Medicinal Chemistry13 citations Open access
Semantic Scholar
Novel ATP Agonists Reveal Receptor Heterogeneity Within P2X and P2Y Subtypes
K. Jacobson, B. Fischer, M. Maillard, J. Boyer +3 more
19956 citations
Semantic Scholar
Synthesis and evaluation of new 2′,3′-dideoxynucleoside analogs as potential anti-AIDS and anti-herpes drugs
A. Faraj, M. Maillard, M. Lemaitre, S. Letellier +5 more
19926 citations
Semantic Scholar
Orthosteric inhibition of MutSβ ATPase function: First disclosure of MSH3-bound small molecule inhibitors.
Gareth N Brace, Karsten Tillack, Peter D. Johnson, Markus Ritzefeld +21 more
2025Bioorganic & Medicinal Chemistry Letters3 citations
Semantic Scholar
Preparation and anti-HIV activity of N-3 amino substituted thymidine nucleoside analogs
M. Maillard, J. Florent, M. Lemaitre, F. Bégassat +8 more
19923 citations
Semantic Scholar
Development and characterization of a CNS-penetrant benzhydryl hydroxamic acid class IIa histone deacetylase inhibitor
C. Luckhurst, M. Maillard, C. Dominguez
20182 citations Open access
Semantic Scholar
A Label-Free LC/MS/MS-Based Enzymatic Activity Assay for the Detection of Genuine Caspase Inhibitors and SAR Development
M. Maillard, C. Dominguez, M. Gemkow, F. Krieger +4 more
2013Journal of biomolecular screening2 citations Open access
Semantic Scholar
PHOTOLABILE A1-ADENOSINE RECEPTOR AGONISTS AS "CAGED" ELECTROPHYSIOLOGICAL PROBES.
M. Maillard, L. Arlinghaus, M. Glashofer, Kevin Y. Lee +1 more
1991Medicinal Chemistry Research1 citations
Semantic Scholar
Design, synthesis, and biological evaluation of potent and selective Class IIa HDAC inhibitors as a potential therapy for Huntington's disease
R. Bürli, C. Luckhurst, O. Aziz, K. Matthews +26 more
20130 citations
Semantic Scholar
Crystal structure of active caspase-6 in complex with Ac-VEID-CHO inhibitor
I. Mueller, M. Lamers, A. Ritchie, C. Dominguez +3 more
20110 citations
Semantic Scholar
Caspase-6 in complex with Z-VAD-FMK inhibitor
I. Mueller, M. Lamers, A. Ritchie, H. Park +4 more
20110 citations
Semantic Scholar
Crystal structure of apo-caspase-6 at physiological pH
I. Mueller, M. Lamers, A. Ritchie, C. Dominguez +3 more
20110 citations
Semantic Scholar
Preparation and anti-HIV Activity of N-3-Substituted Thymidine Nucleoside Analogues.
M. Maillard, J. Florent, M. Lemaitre, F. Bégassat +8 more
20100 citations
Semantic Scholar
Synthesis and Evaluation of New 2′,3′-Dideoxynucleoside Analogues as Potential Anti-AIDS and Anti-Herpes Drugs.
A. Faraj, M. Maillard, M. Lemaitre, S. Letellier +5 more
20100 citations
Semantic Scholar
2-Acetyl-1,3-diaminoalkanes hindroxi
S. Pulley, M. Maillard, E. Baldwin, J. Beck +3 more
20030 citations
Semantic Scholar
Compounds for the treatment of disease alzheimerischen
Y. Fang, R. K. Hom, V. John, M. Maillard
20010 citations
Semantic Scholar
Synthesis of 3′-Substituted-2′,3′-Dideoxynucleoside Analogues as Potential anti-AIDS Drugs.
M. Maillard, A. Faraj, F. Frappier, J. Florent +2 more
19890 citations
Semantic Scholar

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