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TSPO and amyloid deposits in sub-regions of the hippocampus in the 3xTgAD mouse model of Alzheimer’s disease

Neurobiology of disease, 2019-01, Vol.121, p.95-105

2019

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Selective ortho-Bromination of Substituted Benzaldoximes Using Pd-Catalyzed C–H Activation: Application to the Synthesis of Substituted 2-Bromobenzaldehydes

Journal of organic chemistry, 2011-08, Vol.76 (15), p.6414-6420

2011

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Low-dose brain irradiation normalizes TSPO and CLUSTERIN levels and promotes the non-amyloidogenic pathway in pre-symptomatic TgF344-AD rats

Journal of neuroinflammation, 2022-12, Vol.19 (1), p.311-311, Article 311

2022

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Room-Temperature ortho-Alkoxylation and -Halogenation of N-Tosylbenzamides by Using Palladium(II)-Catalyzed CH Activation

Chemistry : a European journal, 2014-06, Vol.20 (24), p.7507-7513

2014

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Synthesis and Structure–Affinity Relationships of Selective High-Affinity 5‑HT4 Receptor Antagonists: Application to the Design of New Potential Single Photon Emission Computed Tomography Tracers

Journal of medicinal chemistry, 2012-11, Vol.55 (22), p.9693-9707

2012

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Reactive astrocytes mediate TSPO overexpression in response to sustained CNTF exposure in the rat striatum

Molecular brain, 2023-07, Vol.16 (1), p.57-57, Article 57

2023

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N-Tosylcarboxamide as a Transformable Directing Group for Pd-Catalyzed C–H Ortho-Arylation

Organic letters, 2012-04, Vol.14 (7), p.1827-1829

2012

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Alterations in dopamine system and in its connectivity with serotonin in a rat model of Alzheimer’s disease

Brain communications, 2021-01, Vol.3 (2), p.fcab029-fcab029

2021

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Iodoindazoles with Selective Magnesiation at Position 3: A Route to Highly Functionalized Indazoles

Chemistry : a European journal, 2016-03, Vol.22 (13), p.4440-4446

2016

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Biotin-conjugated N-methylisatoic anhydride: a chemical tool for nucleic acid separation by selective 2'-hydroxyl acylation of RNA

Chemical communications (Cambridge, England), 2014-01, Vol.50 (43), p.5748-5751

2014

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Room-Temperature ortho-Alkoxylation and -Halogenation of N-Tosylbenzamides by Using Palladium(II)-Catalyzed CH Activation

Chemistry : a European journal, 2014-06, Vol.20 (24), p.7507

2014

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Efficient Room-Temperature One-Pot Synthesis of 2-Amino-3-alkyl(3-aryl)quinazolin-4(3H)-ones

European Journal of Organic Chemistry, 2011-05, Vol.2011 (15), p.2785-2788

2011

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Design of a serotonin 4 receptor radiotracer with decreased lipophilicity for single photon emission computed tomography

European journal of medicinal chemistry, 2015-04, Vol.94, p.386-396

2015

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Synthesis and Anti-HIV Activity of Some [Nucleoside Reverse Transcriptase Inhibitor]-C5′-Linker-[Integrase Inhibitor] Heterodimers as Inhibitors of HIV Replication

Journal of enzyme inhibition and medicinal chemistry, 2004-12, Vol.19 (6), p.497-509

2004

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Design of fluorinated 5-HT4R antagonists: Influence of the basicity and lipophilicity toward the 5-HT4R binding affinities

Bioorganic & medicinal chemistry, 2013-12, Vol.21 (23), p.7529-7538

2013

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A convenient microwave-assisted 5-amination of flavones

Tetrahedron, 2008-12, Vol.64 (49), p.11243-11248

2008

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Synthesis and Structure–Affinity Relationships of Selective High-Affinity 5-HT 4 Receptor Antagonists: Application to the Design of New Potential Single Photon Emission Computed Tomography Tracers

Journal of medicinal chemistry, 2012-11, Vol.55 (22), p.9693-9707

2012

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Design of fluorinated 5-HT(4)R antagonists: influence of the basicity and lipophilicity toward the 5-HT(4)R binding affinities

Bioorganic & medicinal chemistry, 2013-12, Vol.21 (23), p.7529-7538

2013

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Synthesis of prodrug-type anti-HIV agents conjugating a REVERSE transcriptase inhibitor to a HIV-1 integrase inhibitor by a spontaneously cleavable linker

Journal of enzyme inhibition and medicinal chemistry, 2007-10, Vol.22 (5), p.591-607

2007

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Synthesis and structure-affinity relationships of selective high-affinity 5-HT(4) receptor antagonists: application to the design of new potential single photon emission computed tomography tracers

Journal of medicinal chemistry, 2012-11, Vol.55 (22), p.9693-9707

2012

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Synthesis and anti-HIV evaluation of hybrid-type prodrugs conjugating HIV integrase inhibitors with d4t by self-cleavable spacers containing an amino acid residue

Journal of enzyme inhibition and medicinal chemistry, 2007-10, Vol.22 (5), p.608-619

2007

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Synthesis and antiviral activity of aryl phosphoramidate derivatives of β-D- and β-L-C-5-Substituted 2',3'-didehydro-2',3'-dideoxy-uridine bearing linker arms

Journal of enzyme inhibition and medicinal chemistry, 2005-12, Vol.20 (6), p.533-549

2005

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Synthesis and Anti-HIV Activity of Some Heterodimers [NRTI]-Glycyl-Succinyl-[Trovirdine Analogue] of Known HIV-1 Reverse Transcriptase Inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2003-04, Vol.18 (2), p.175-186

2003

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ChemInform Abstract: Iodoindazoles with Selective Magnesiation at Position 3: A Route to Highly Functionalized Indazoles

ChemInform, 2016-07, Vol.47 (32), p.no-no

2016

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ChemInform Abstract: N-Tosylcarboxamide as a Transformable Directing Group for Pd-Catalyzed C-H ortho-Arylation

ChemInform, 2012-07, Vol.43 (31), p.no-no

2012

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TSPO and amyloid deposits in sub-regions of the hippocampus in the 3xTgAD mouse model of Alzheimer’s disease

Selective ortho-Bromination of Substituted Benzaldoximes Using Pd-Catalyzed C–H Activation: Application to the Synthesis of Substituted 2-Bromobenzaldehydes

Low-dose brain irradiation normalizes TSPO and CLUSTERIN levels and promotes the non-amyloidogenic pathway in pre-symptomatic TgF344-AD rats

Room-Temperature ortho-Alkoxylation and -Halogenation of N-Tosylbenzamides by Using Palladium(II)-Catalyzed CH Activation

Synthesis and Structure–Affinity Relationships of Selective High-Affinity 5‑HT4 Receptor Antagonists: Application to the Design of New Potential Single Photon Emission Computed Tomography Tracers

Reactive astrocytes mediate TSPO overexpression in response to sustained CNTF exposure in the rat striatum

N-Tosylcarboxamide as a Transformable Directing Group for Pd-Catalyzed C–H Ortho-Arylation

Alterations in dopamine system and in its connectivity with serotonin in a rat model of Alzheimer’s disease

Iodoindazoles with Selective Magnesiation at Position 3: A Route to Highly Functionalized Indazoles

Biotin-conjugated N-methylisatoic anhydride: a chemical tool for nucleic acid separation by selective 2'-hydroxyl acylation of RNA

Room-Temperature ortho-Alkoxylation and -Halogenation of N-Tosylbenzamides by Using Palladium(II)-Catalyzed CH Activation

Efficient Room-Temperature One-Pot Synthesis of 2-Amino-3-alkyl(3-aryl)quinazolin-4(3H)-ones

Design of a serotonin 4 receptor radiotracer with decreased lipophilicity for single photon emission computed tomography

Synthesis and Anti-HIV Activity of Some [Nucleoside Reverse Transcriptase Inhibitor]-C5′-Linker-[Integrase Inhibitor] Heterodimers as Inhibitors of HIV Replication

Design of fluorinated 5-HT4R antagonists: Influence of the basicity and lipophilicity toward the 5-HT4R binding affinities

A convenient microwave-assisted 5-amination of flavones

Synthesis and Structure–Affinity Relationships of Selective High-Affinity 5-HT 4 Receptor Antagonists: Application to the Design of New Potential Single Photon Emission Computed Tomography Tracers

Design of fluorinated 5-HT(4)R antagonists: influence of the basicity and lipophilicity toward the 5-HT(4)R binding affinities

Synthesis of prodrug-type anti-HIV agents conjugating a REVERSE transcriptase inhibitor to a HIV-1 integrase inhibitor by a spontaneously cleavable linker

Synthesis and structure-affinity relationships of selective high-affinity 5-HT(4) receptor antagonists: application to the design of new potential single photon emission computed tomography tracers

Synthesis and anti-HIV evaluation of hybrid-type prodrugs conjugating HIV integrase inhibitors with d4t by self-cleavable spacers containing an amino acid residue

Synthesis and antiviral activity of aryl phosphoramidate derivatives of β-D- and β-L-C-5-Substituted 2',3'-didehydro-2',3'-dideoxy-uridine bearing linker arms

Synthesis and Anti-HIV Activity of Some Heterodimers [NRTI]-Glycyl-Succinyl-[Trovirdine Analogue] of Known HIV-1 Reverse Transcriptase Inhibitors

ChemInform Abstract: Iodoindazoles with Selective Magnesiation at Position 3: A Route to Highly Functionalized Indazoles

ChemInform Abstract: N-Tosylcarboxamide as a Transformable Directing Group for Pd-Catalyzed C-H ortho-Arylation

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