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Sub-minimum inhibitory concentrations of colistin and polymyxin B promote Acinetobacter baumannii biofilm formation

PloS one, 2018-03, Vol.13 (3), p.e0194556-e0194556

2018

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Multidrug-resistant Acinetobacter baumannii resists reactive oxygen species and survives in macrophages

Scientific reports, 2019-11, Vol.9 (1), p.17462-12, Article 17462

2019

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Structurally Novel Highly Potent Proteasome Inhibitors Created by the Structure-Based Hybridization of Nonpeptidic Belactosin Derivatives and Peptide Boronates

Journal of medicinal chemistry, 2014-03, Vol.57 (6), p.2726-2735

2014

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Lipopolysaccharide-Deficient Acinetobacter baumannii Due to Colistin Resistance Is Killed by Neutrophil-Produced Lysozyme

Frontiers in microbiology, 2020-04, Vol.11, p.573-573

2020

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Longevity control by supersulfide-mediated mitochondrial respiration and regulation of protein quality

Redox biology, 2024-02, Vol.69, p.103018, Article 103018

2024

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Potent Proteasome Inhibitors Derived from the Unnatural cis-Cyclopropane Isomer of Belactosin A: Synthesis, Biological Activity, and Mode of Action

Journal of medicinal chemistry, 2013-05, Vol.56 (9), p.3689-3700

2013

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The dynamic structure of Rab35 is stabilized in the presence of GTP under physiological conditions

Biochemistry and biophysics reports, 2020-09, Vol.23, p.100776-100776, Article 100776

2020

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Investigation of the Noncovalent Binding Mode of Covalent Proteasome Inhibitors around the Transition State by Combined Use of Cyclopropylic Strain-Based Conformational Restriction and Computational Modeling

Journal of medicinal chemistry, 2013-07, Vol.56 (14), p.5829-5842

2013

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Acinetobacter baumannii Lipopolysaccharide Influences Adipokine Expression in 3T3-L1 Adipocytes

Mediators of inflammation, 2017-01, Vol.2017 (2017), p.1-9

2017

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Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy

Organic & biomolecular chemistry, 2009-01, Vol.7 (9), p.1868-1877

2009

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Identification of novel kynurenine production-inhibiting benzenesulfonamide derivatives in cancer cells

Biochemical and biophysical research communications, 2012-03, Vol.419 (3), p.556-561

2012

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Identification of a small-molecule inhibitor of the interaction between Survivin and Smac/DIABLO

Biochemical and biophysical research communications, 2010-03, Vol.393 (2), p.253-258

2010

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Immunomodulatory gene expression analysis in LPS-stimulated human polymorphonuclear leukocytes treated with antibiotics commonly used for multidrug-resistant strains

Molecular immunology, 2021-01, Vol.129, p.39-44

2021

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Virulence characteristics of Acinetobacter baumannii clinical isolates vary with the expression levels of omps

Journal of medical microbiology, 2017-02, Vol.66 (2), p.203-212

2017

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Novel candesartan derivatives as indoleamine 2,3-dioxygenase inhibitors

MedChemComm, 2012, Vol.3 (4), p.475

2012

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Advanced glycation end products-modified proteins and oxidized LDL mediate down-regulation of leptin in mouse adipocytes via CD36

Biochemical and biophysical research communications, 2004-12, Vol.325 (1), p.151-156

2004

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Pathological Roles of Advanced Glycation End Product Receptors SR-A and CD36

Annals of the New York Academy of Sciences, 2005-06, Vol.1043 (1), p.671-675

2005

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Palmitoyl lactic acid induces adipogenesis and a brown fat-like phenotype in 3T3-L1 preadipocytes

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2018-07, Vol.1863 (7), p.772-782

2018

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Resolvin E1, but not resolvins E2 and E3, promotes fMLF‐induced ROS generation in human neutrophils

FEBS letters, 2018-08, Vol.592 (16), p.2706-2715

2018

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Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structure

Organic & biomolecular chemistry, 2013-10, Vol.11 (38), p.6615-6622

2013

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Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones

Bioorganic & medicinal chemistry, 2014-06, Vol.22 (12), p.3091-3095

2014

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Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin A

Chemical communications (Cambridge, England), 2014-03, Vol.50 (19), p.2445-2447

2014

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S-Benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (17), p.5126-5129

2010

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Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structureElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob41338a

2013-09

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Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin AElectronic supplementary information (ESI) available. See DOI: 10.1039/c3cc48818g

2014-02

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Sub-minimum inhibitory concentrations of colistin and polymyxin B promote Acinetobacter baumannii biofilm formation

Multidrug-resistant Acinetobacter baumannii resists reactive oxygen species and survives in macrophages

Structurally Novel Highly Potent Proteasome Inhibitors Created by the Structure-Based Hybridization of Nonpeptidic Belactosin Derivatives and Peptide Boronates

Lipopolysaccharide-Deficient Acinetobacter baumannii Due to Colistin Resistance Is Killed by Neutrophil-Produced Lysozyme

Longevity control by supersulfide-mediated mitochondrial respiration and regulation of protein quality

Potent Proteasome Inhibitors Derived from the Unnatural cis-Cyclopropane Isomer of Belactosin A: Synthesis, Biological Activity, and Mode of Action

The dynamic structure of Rab35 is stabilized in the presence of GTP under physiological conditions

Investigation of the Noncovalent Binding Mode of Covalent Proteasome Inhibitors around the Transition State by Combined Use of Cyclopropylic Strain-Based Conformational Restriction and Computational Modeling

Acinetobacter baumannii Lipopolysaccharide Influences Adipokine Expression in 3T3-L1 Adipocytes

Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy

Identification of novel kynurenine production-inhibiting benzenesulfonamide derivatives in cancer cells

Identification of a small-molecule inhibitor of the interaction between Survivin and Smac/DIABLO

Immunomodulatory gene expression analysis in LPS-stimulated human polymorphonuclear leukocytes treated with antibiotics commonly used for multidrug-resistant strains

Virulence characteristics of Acinetobacter baumannii clinical isolates vary with the expression levels of omps

Novel candesartan derivatives as indoleamine 2,3-dioxygenase inhibitors

Advanced glycation end products-modified proteins and oxidized LDL mediate down-regulation of leptin in mouse adipocytes via CD36

Pathological Roles of Advanced Glycation End Product Receptors SR-A and CD36

Palmitoyl lactic acid induces adipogenesis and a brown fat-like phenotype in 3T3-L1 preadipocytes

Resolvin E1, but not resolvins E2 and E3, promotes fMLF‐induced ROS generation in human neutrophils

Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structure

Development of a new class of proteasome inhibitors with an epoxyketone warhead: Rational hybridization of non-peptidic belactosin derivatives and peptide epoxyketones

Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin A

S-Benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase

Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structureElectronic supplementary information (ESI) available. See DOI: 10.1039/c3ob41338a

Rational hopping of a peptidic scaffold into non-peptidic scaffolds: structurally novel potent proteasome inhibitors derived from a natural product, belactosin AElectronic supplementary information (ESI) available. See DOI: 10.1039/c3cc48818g

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