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MAIT cell-directed therapy of Mycobacterium tuberculosis infection

Mucosal immunology, 2021-01, Vol.14 (1), p.199-208

2021

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Discovery and Target Identification of an Antiproliferative Agent in Live Cells Using Fluorescence Difference in Two-Dimensional Gel Electrophoresis

Angewandte Chemie (International ed.), 2012-05, Vol.51 (22), p.5447-5451

International ed. in English, 2012

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Tuberculosis Drug Discovery: A Decade of Hit Assessment for Defined Targets

Frontiers in cellular and infection microbiology, 2021-03, Vol.11, p.611304-611304

2021

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The Antitubercular Activities of Natural Products with Fused-Nitrogen-Containing Heterocycles

Pharmaceuticals (Basel, Switzerland), 2024-02, Vol.17 (2), p.211

2024

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Functional inactivation of pulmonary MAIT cells following 5-OP-RU treatment of non-human primates

Mucosal immunology, 2021-09, Vol.14 (5), p.1055-1066

2021

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A design strategy for drug-like polyheterocycles with privileged substructures for discovery of specific small-molecule modulators

Chemical communications (Cambridge, England), 2011-12, Vol.47 (48), p.12754-12761

2011

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Structure–Activity Relationships of Pyrazolo[1,5‑a]pyrimidin-7(4H)‑ones as Antitubercular Agents

ACS infectious diseases, 2021-02, Vol.7 (2), p.479-492

2021

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cdc-25.4, a Caenorhabditis elegans Ortholog of cdc25, Is Required for Male Mating Behavior

G3 : genes - genomes - genetics, 2016-12, Vol.6 (12), p.4127-4138

2016

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Anti-obesity agents: a focused review on the structural classification of therapeutic entities

Current topics in medicinal chemistry, 2009-04, Vol.9 (6), p.466-481

2009

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Chemical approaches to unraveling the biology of mycobacteria

Cell chemical biology, 2023-05, Vol.30 (5), p.420-435

2023

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Phenotype-based screening rediscovered benzopyran-embedded microtubule inhibitors as anti-neuroinflammatory agents by modulating the tubulin-p65 interaction

Experimental & molecular medicine, 2022-12, Vol.54 (12), p.2200-2209

2022

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Abstract 68: Activating mucosal-associated invariant T cells (MAITs) induces a broad anti-tumor response and offers a novel target for cancer immunotherapy

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.68-68

2021

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Discovery and Structure–Activity-Relationship Study of N‑Alkyl-5-hydroxypyrimidinone Carboxamides as Novel Antitubercular Agents Targeting Decaprenylphosphoryl-β‑d‑ribose 2′-Oxidase

Journal of medicinal chemistry, 2018-11, Vol.61 (22), p.9952-9965

2018

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Discovery of 4H-chromeno[2,3-d]pyrimidin-4-one derivatives as senescence inducers and their senescence-associated antiproliferative activities on cancer cells using advanced phenotypic assay

European journal of medicinal chemistry, 2021-01, Vol.209, p.112550, Article 112550

2021

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cdc-25.2, a Caenorhabditis elegans ortholog of cdc25, is required for male tail morphogenesis

Biochemical and biophysical research communications, 2017-01, Vol.482 (4), p.1213-1218

2017

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Nonspecific protein labeling of photoaffinity linkers correlates with their molecular shapes in living cells

Chemical communications (Cambridge, England), 2016-04, Vol.52 (34), p.5828-5831

2016

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Discovery of Carbohybrid-Based 2‑Aminopyrimidine Analogues As a New Class of Rapid-Acting Antimalarial Agents Using Image-Based Cytological Profiling Assay

Journal of medicinal chemistry, 2014-09, Vol.57 (17), p.7425-7434

2014

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Synthesis and biological evaluation of 2,3-dihydroimidazo[1,2-a]benzimidazole derivatives against Leishmania donovani and Trypanosoma cruzi

European journal of medicinal chemistry, 2014-09, Vol.84, p.395-403

2014

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Cover Picture: Discovery and Target Identification of an Antiproliferative Agent in Live Cells Using Fluorescence Difference in Two-Dimensional Gel Electrophoresis (Angew. Chem. Int. Ed. 22/2012)

Angewandte Chemie (International ed.), 2012-05, Vol.51 (22), p.5259-5259

International ed. in English, 2012

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Activating Mucosal-Associated Invariant T Cells Induces a Broad Antitumor Response

Cancer immunology research, 2021-09, Vol.9 (9), p.1024-1034

2021

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Identification of Piperidine-3-carboxamide Derivatives Inducing Senescence-like Phenotype with Antimelanoma Activities

ACS medicinal chemistry letters, 2021-04, Vol.12 (4), p.563-571

2021

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Inhibition of CorA-Dependent Magnesium Homeostasis Is Cidal in Mycobacterium tuberculosis

Antimicrobial agents and chemotherapy, 2019-10, Vol.63 (10)

2019

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Synthesis and Structure–Activity Relationships of a New Class of Oxadiazoles Targeting DprE1 as Antitubercular Agents

ACS medicinal chemistry letters, 2023-09, Vol.14 (9), p.1275-1283

2023

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Nonspecific protein labeling of photoaffinity linkers correlates with their molecular shapes in living cellsElectronic supplementary information (ESI) available: Synthetic procedures, spectroscopic data of all new compounds, and procedures for biological experiment. See DOI: 10.1039/c6cc01426g

2016-04

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Transcriptional Corepressor SMILE Recruits SIRT1 to Inhibit Nuclear Receptor Estrogen Receptor-related Receptor γ Transactivation

The Journal of biological chemistry, 2009-10, Vol.284 (42), p.28762-28774

2009

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MAIT cell-directed therapy of Mycobacterium tuberculosis infection

Discovery and Target Identification of an Antiproliferative Agent in Live Cells Using Fluorescence Difference in Two-Dimensional Gel Electrophoresis

Tuberculosis Drug Discovery: A Decade of Hit Assessment for Defined Targets

The Antitubercular Activities of Natural Products with Fused-Nitrogen-Containing Heterocycles

Functional inactivation of pulmonary MAIT cells following 5-OP-RU treatment of non-human primates

A design strategy for drug-like polyheterocycles with privileged substructures for discovery of specific small-molecule modulators

Structure–Activity Relationships of Pyrazolo[1,5‑a]pyrimidin-7(4H)‑ones as Antitubercular Agents

cdc-25.4, a Caenorhabditis elegans Ortholog of cdc25, Is Required for Male Mating Behavior

Anti-obesity agents: a focused review on the structural classification of therapeutic entities

Chemical approaches to unraveling the biology of mycobacteria

Phenotype-based screening rediscovered benzopyran-embedded microtubule inhibitors as anti-neuroinflammatory agents by modulating the tubulin-p65 interaction

Abstract 68: Activating mucosal-associated invariant T cells (MAITs) induces a broad anti-tumor response and offers a novel target for cancer immunotherapy

Discovery and Structure–Activity-Relationship Study of N‑Alkyl-5-hydroxypyrimidinone Carboxamides as Novel Antitubercular Agents Targeting Decaprenylphosphoryl-β‑d‑ribose 2′-Oxidase

Discovery of 4H-chromeno[2,3-d]pyrimidin-4-one derivatives as senescence inducers and their senescence-associated antiproliferative activities on cancer cells using advanced phenotypic assay

cdc-25.2, a Caenorhabditis elegans ortholog of cdc25, is required for male tail morphogenesis

Nonspecific protein labeling of photoaffinity linkers correlates with their molecular shapes in living cells

Discovery of Carbohybrid-Based 2‑Aminopyrimidine Analogues As a New Class of Rapid-Acting Antimalarial Agents Using Image-Based Cytological Profiling Assay

Synthesis and biological evaluation of 2,3-dihydroimidazo[1,2-a]benzimidazole derivatives against Leishmania donovani and Trypanosoma cruzi

Cover Picture: Discovery and Target Identification of an Antiproliferative Agent in Live Cells Using Fluorescence Difference in Two-Dimensional Gel Electrophoresis (Angew. Chem. Int. Ed. 22/2012)

Activating Mucosal-Associated Invariant T Cells Induces a Broad Antitumor Response

Identification of Piperidine-3-carboxamide Derivatives Inducing Senescence-like Phenotype with Antimelanoma Activities

Inhibition of CorA-Dependent Magnesium Homeostasis Is Cidal in Mycobacterium tuberculosis

Synthesis and Structure–Activity Relationships of a New Class of Oxadiazoles Targeting DprE1 as Antitubercular Agents

Nonspecific protein labeling of photoaffinity linkers correlates with their molecular shapes in living cellsElectronic supplementary information (ESI) available: Synthetic procedures, spectroscopic data of all new compounds, and procedures for biological experiment. See DOI: 10.1039/c6cc01426g

Transcriptional Corepressor SMILE Recruits SIRT1 to Inhibit Nuclear Receptor Estrogen Receptor-related Receptor γ Transactivation

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