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Multimode, Cooperative Mechanism of Action of Allosteric HIV-1 Integrase Inhibitors

The Journal of biological chemistry, 2012-05, Vol.287 (20), p.16801-16811

2012

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A new class of multimerization selective inhibitors of HIV-1 integrase

PLoS pathogens, 2014-05, Vol.10 (5), p.e1004171

2014

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Indole-based allosteric inhibitors of HIV-1 integrase

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19), p.4748-4752

2016

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Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis

Journal of natural products (Washington, D.C.), 2013-03, Vol.76 (3), p.394-404

2013

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First Insight on Small Molecules as Cardiac Calsequestrin Stabilizers

ACS omega, 2019-07, Vol.4 (7), p.11508-11514

2019

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Calcium-BINOL: a novel and efficient catalyst for asymmetric Michael reactions

Tetrahedron letters, 2001-11, Vol.42 (48), p.8515-8517

2001

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Enantioenriched Calcium-(R)-5,5′,6,6′,7,7′,8,8′-Octahydro-BINOL (H8-BINOL): An Efficient Catalyst for the Creation of a Quaternary Stereocenter

Advanced synthesis & catalysis, 2005-05, Vol.347 (6), p.867-871

2005

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Recent advancements in pharmacological strategies to modulate energy balance for combating obesity

RSC medicinal chemistry, 2023-08, Vol.14 (8), p.1429-1445

2023

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The role of polyplexes in developing a green sustainable approach in agriculture

RSC advances, 2022-11, Vol.12 (53), p.34463-34481

2022

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Synthesis of Stannylated Allyl- and Vinylphosphonates via Molybdenum-Catalyzed Hydrostannations

European Journal of Organic Chemistry, 2008-08, Vol.2008 (22), p.3852-3858

2008

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Enantioenriched calcium complexes mediated efficient synthesis of (S)-(+)-fenoprofen

ARKIVOC, 2005-09, Vol.2005 (15), p.53-58

2005

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The mechanism of H171T resistance reveals the importance of Nδ-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

Retrovirology, 2014-11, Vol.11 (1), p.100, Article 100

2014

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The C-terminal calcium-sensitive disordered motifs regulate isoform-specific polymerization characteristics of calsequestrin

Biopolymers, 2015-01, Vol.103 (1), p.15-22

2015

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The Catecholaminergic Polymorphic Ventricular Tachycardia Mutation R33Q Disrupts the N-terminal Structural Motif That Regulates Reversible Calsequestrin Polymerization

The Journal of biological chemistry, 2010-05, Vol.285 (22), p.17188-17196

2010

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Identification of calcium binding sites on calsequestrin 1 and their implications for polymerization

Molecular bioSystems, 2013-01, Vol.9 (7), p.1949-1957

2013

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Probing cationic selectivity of cardiac calsequestrin and its CPVT mutants

Biochemical journal, 2011-04, Vol.435 (2), p.391-399

2011

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Skeletal Calsequestrin - Calcium Interaction: Role of Acidic C-Terminus

Biophysical journal, 2013-01, Vol.104 (2), p.173a-173a

2013

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Aromatic interaction profile to understand the molecular basis of raltegravir resistance

Structural chemistry, 2013-10, Vol.24 (5), p.1499-1512

2013

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A New Class of Multimerization Selective Inhibitors of HIV-1 Integrase: e1004171

PLoS pathogens, 2014-05, Vol.10 (5)

2014

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An Alternately Charged Residue Cluster at the N-terminal End Forms a Ring System and Dynamically Regulates Calsequestrin Polymerization

Biophysical journal, 2010-01, Vol.98 (3), p.634a-634a

2010

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The mechanism of H171T resistance reveals the importance of N[delta]-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

Retrovirology, 2014-11, Vol.11

2014

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Identification of calcium binding sites on calsequestrin 1 and their implications for polymerizationElectronic supplementary information (ESI) available. See DOI: 10.1039/c3mb25588c

2013-06

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Oppolzer Sultam Directed Aldol as a Key Step for the Stereoselective Syntheses of Antitumor Antibiotic Belactosin C and Its Synthetic Congeners

Journal of organic chemistry, 2006-01, Vol.71 (1), p.337-340

2006

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Identification of Calcium binding sites on calsequestrin 1 and its implications to polymerization

Molecular bioSystems, 2013-04, Vol.9 (7), p.1949-1957

2013

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The mechanism of H171T resistance reveals the importance of N sub( delta )-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

Retrovirology, 2014-01, Vol.11 (1), p.100-100

2014

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Multimode, Cooperative Mechanism of Action of Allosteric HIV-1 Integrase Inhibitors

A new class of multimerization selective inhibitors of HIV-1 integrase

Indole-based allosteric inhibitors of HIV-1 integrase

Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis

First Insight on Small Molecules as Cardiac Calsequestrin Stabilizers

Calcium-BINOL: a novel and efficient catalyst for asymmetric Michael reactions

Enantioenriched Calcium-(R)-5,5′,6,6′,7,7′,8,8′-Octahydro-BINOL (H8-BINOL): An Efficient Catalyst for the Creation of a Quaternary Stereocenter

Recent advancements in pharmacological strategies to modulate energy balance for combating obesity

The role of polyplexes in developing a green sustainable approach in agriculture

Synthesis of Stannylated Allyl- and Vinylphosphonates via Molybdenum-Catalyzed Hydrostannations

Enantioenriched calcium complexes mediated efficient synthesis of (S)-(+)-fenoprofen

The mechanism of H171T resistance reveals the importance of Nδ-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

The C-terminal calcium-sensitive disordered motifs regulate isoform-specific polymerization characteristics of calsequestrin

The Catecholaminergic Polymorphic Ventricular Tachycardia Mutation R33Q Disrupts the N-terminal Structural Motif That Regulates Reversible Calsequestrin Polymerization

Identification of calcium binding sites on calsequestrin 1 and their implications for polymerization

Probing cationic selectivity of cardiac calsequestrin and its CPVT mutants

Skeletal Calsequestrin - Calcium Interaction: Role of Acidic C-Terminus

Aromatic interaction profile to understand the molecular basis of raltegravir resistance

A New Class of Multimerization Selective Inhibitors of HIV-1 Integrase: e1004171

An Alternately Charged Residue Cluster at the N-terminal End Forms a Ring System and Dynamically Regulates Calsequestrin Polymerization

The mechanism of H171T resistance reveals the importance of N[delta]-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

Identification of calcium binding sites on calsequestrin 1 and their implications for polymerizationElectronic supplementary information (ESI) available. See DOI: 10.1039/c3mb25588c

Oppolzer Sultam Directed Aldol as a Key Step for the Stereoselective Syntheses of Antitumor Antibiotic Belactosin C and Its Synthetic Congeners

Identification of Calcium binding sites on calsequestrin 1 and its implications to polymerization

The mechanism of H171T resistance reveals the importance of N sub( delta )-protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase

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