M. Elofsson

发表

Discovery of ligands for ADP-ribosyltransferases via docking-based virtual screening.

C. D. Andersson, A. Linusson, J. Weigelt, 2012, Journal of medicinal chemistry.

Type III secretion inhibitors for the management of bacterial plant diseases.

M. Valls, Rohan A. Davis, Montserrat Solé, 2018, Molecular plant pathology.

Inhibitory Activity of the Isoflavone Biochanin A on Intracellular Bacteria of Genus Chlamydia and Initial Development of a Buccal Formulation

N. Sandler, P. Vuorela, J. Salonen, 2014, PloS one.

Salicylidene Acylhydrazides That Affect Type III Protein Secretion in Salmonella enterica Serovar Typhimurium

H. Wolf‐Watz, A. Negrea, M. Rhen, 2007, Antimicrobial Agents and Chemotherapy.

Identification of Small Molecules Blocking the Pseudomonas aeruginosa Type III Secretion System Protein PcrV

S. Spjut, M. Elofsson, C. Sundin, 2021, Biomolecules.

Inhibitors of type III secretion in Yersinia: design, synthesis and multivariate QSAR of 2-arylsulfonylamino-benzanilides.

C. D. Andersson, A. Linusson, M. Elofsson, 2007, Bioorganic & medicinal chemistry.

Preparation of building blocks for glycopeptide synthesis by glycosylation of Fmoc amino acids having unprotected carboxyl groups

J. Kihlberg, M. Elofsson, L. A. Salvador, 1995 .

Towards subunit-specific proteasome inhibitors: synthesis and evaluation of peptide α', β'-epoxyketones

C. Crews, U. Splittgerber, M. Elofsson, 1999 .

Fluorescent Molecularly Imprinted Polymer Layers against Sialic Acid on Silica-Coated Polystyrene Cores—Assessment of the Binding Behavior to Cancer Cells

K. Rurack, J. Persson, P. Härkönen, 2022, Cancers.

Building blocks for glycopeptide synthesis: Preparation of α-O-fucosylated fmoc serine and threonine in one step from L-fucose tetraacetate

J. Kihlberg, M. Elofsson, L. A. Salvador, 1996 .

Multivalent HSA Conjugates of 3′‐Sialyllactose are Potent Inhibitors of Adenoviral Cell Attachment and Infection

J. Kihlberg, G. Wadell, N. Arnberg, 2005, Chembiochem : a European journal of chemical biology.

Sialic Acid-Containing Glycans as Cellular Receptors for Ocular Human Adenoviruses: Implications for Tropism and Treatment

N. Chandra, N. Arnberg, M. Elofsson, 2019, Viruses.

A Potent Trivalent Sialic Acid Inhibitor of Adenovirus Type 37 Infection of Human Corneal Cells**

T. Stehle, N. Arnberg, J. Bauer, 2011, Angewandte Chemie.

The Resveratrol Tetramer (-)-Hopeaphenol Inhibits Type III Secretion in the Gram-Negative Pathogens Yersinia pseudotuberculosis and Pseudomonas aeruginosa

R. Quinn, Rohan A. Davis, M. Elofsson, 2013, PloS one.

Sialic acid as a biomarker studied in breast cancer cells using fluorescent molecularly imprinted polymers, MIPs

B. Sellergren, Sudhirkumar Shinde, J. Persson, 2020 .

Corticosteroids protect infected cells against mycobacterial killing in vitro.

R. Ummanni, M. Elofsson, Christer Larsson, 2019, Biochemical and biophysical research communications.

Mycobacterium tuberculosis virulence inhibitors discovered by Mycobacterium marinum high-throughput screening

R. Ummanni, M. Elofsson, Christer Larsson, 2019, Scientific Reports.

Solving the supply of resveratrol tetramers from Papua New Guinean rainforest anisoptera species that inhibit bacterial type III secretion systems.

V. Avery, R. Quinn, P. Healy, 2014, Journal of natural products.

Candidate vaginal microbicides with activity against Chlamydia trachomatis and Neisseriagonorrhoeae.

P. Keyser, Anatoly V. Slepenkin, E. Peterson, 2010, International journal of antimicrobial agents.

Specificity of glycopeptide-specific T cells.

E. Unanue, J. Kihlberg, M. Elofsson, 1995, Journal of immunology.

Direct synthesis of glycosylated amino acids from carbohydrate peracetates and Fmoc amino acids: solid-phase synthesis of biomedicinally interesting glycopeptides.

J. Kihlberg, M. Elofsson, L. A. Salvador, 1997, Methods in enzymology.

Building blocks for glycopeptide synthesis: glycosylation of 3-mercaptopropionic acid and Fmoc amino acids with unprotected carboxyl groups

J. Kihlberg, M. Elofsson, B. Walse, 1991 .

Antiviral Activity of Benzavir-2 against Emerging Flaviviruses

M. Evander, M. Elofsson, R. Lindqvist, 2020, Viruses.

Identification of Bacterial Target Proteins for the Salicylidene Acylhydrazide Class of Virulence-blocking Compounds

Brian O. Smith, M. Gabrielsen, O. Byron, 2011, The Journal of Biological Chemistry.

Pentavalent Sialic Acid Conjugates Block Coxsackievirus A24 Variant and Human Adenovirus Type 37–Viruses That Cause Highly Contagious Eye Infections

C. D. Andersson, T. Stehle, Rebecca F. Thompson, 2020, ACS chemical biology.

Solid-phase synthesis and conformational studies of helper T cell immunogenic peptides that carry carbohydrate haptens linked to serine.

J. Kihlberg, M. Elofsson, B. Walse, 2009, International journal of peptide and protein research.

Glycopeptides bind MHC molecules and elicit specific T cell responses.

E. Unanue, J. Kihlberg, C. Harding, 1993, Journal of immunology.

Edinburgh Research Explorer Characterization of the Effects of Salicylidene Acylhydrazide Compounds on Type III Secretion in Escherichia coli O157:H7

M. Stevens, J. Tree, A. Roe, 2022 .

Solid-phase synthesis of serine-based glycosphingolipid analogues for preparation of glycoconjugate arrays.

Annika I Johansson, M. Elofsson, H. A. Norberg, 2005, Organic & biomolecular chemistry.

Anti-Rift Valley fever virus activity in vitro, pre-clinical pharmacokinetics and oral bioavailability of benzavir-2, a broad-acting antiviral compound

P. Artursson, M. Evander, C. Ahlm, 2018, Scientific Reports.

N-Acylated Derivatives of Sulfamethoxazole Block Chlamydia Fatty Acid Synthesis and Interact with FabF

C. D. Andersson, R. Bastidas, R. Valdivia, 2017, Antimicrobial Agents and Chemotherapy.

Formation of lactones from sialylated MUC1 glycopeptides.

J. Kihlberg, C. Reis, M. Elofsson, 2006, Organic & biomolecular chemistry.

A small-molecule inhibitor of type III secretion inhibits different stages of the infectious cycle of Chlamydia trachomatis

S. Normark, S. Bergström, B. Henriques-Normark, 2006, Proceedings of the National Academy of Sciences.

Small molecule inhibitors of type III secretion in Yersinia block the Chlamydia pneumoniae infection cycle

P. Nordström, S. Bergström, B. Henriques-Normark, 2007, FEBS letters.

Removal of Acyl Protective Groups from Glycopeptides: Base Does Not Epimerize Peptide Stereocenters, and beta-Elimination Is Slow.

J. Kihlberg, M. Elofsson, P. Sjölin, 1996, The Journal of organic chemistry.

Total synthesis of the potent proteasome inhibitor epoxomicin: a useful tool for understanding proteasome biology.

C. Crews, B. Kwok, M. Elofsson, 1999, Bioorganic & medicinal chemistry letters.

Novel High-Throughput Screening Method for Identification of Fungal Dimorphism Blockers

C. Urban, M. Elofsson, Hanna Uvell, 2015, Journal of biomolecular screening.

Protection of mice from a Chlamydia trachomatis vaginal infection using a Salicylidene acylhydrazide, a potential microbicide.

P. Keyser, Anatoly V. Slepenkin, E. Peterson, 2011, The Journal of infectious diseases.

Design, synthesis, and multivariate quantitative structure-activity relationship of salicylanilides--potent inhibitors of type III secretion in Yersinia.

Markus K. Dahlgren, A. Linusson, M. Dahlgren, 2007, Journal of medicinal chemistry.

Virulence blockers as alternatives to antibiotics: type III secretion inhibitors against Gram‐negative bacteria

P. Keyser, H. Wolf‐Watz, M. Elofsson, 2008, Journal of internal medicine.

Structure-activity relationships for inhibitors of Pseudomonas aeruginosa exoenzyme S ADP-ribosyltransferase activity.

H. Schüler, M. Elofsson, A. F. Pinto, 2018, European journal of medicinal chemistry.

Synthesis of [4-(2-Hydroxyphenyl)thiazol-2-yl]methanones as Potential Bioisosteres of Salicylidene Acylhydrazides

M. Dahlgren, M. Elofsson, J. Hillgren, 2010, Molecules.

Synthesis of 2-(2-Aminopyrimidine)-2,2-difluoroethanols as Potential Bioisosters of Salicylidene Acylhydrazides

M. Dahlgren, M. Elofsson, E. Wallin, 2010, Molecules.

Exploring divalent conjugates of 5-N-acetyl-neuraminic acid as inhibitors of coxsackievirus A24 variant (CVA24v) transduction

T. Stehle, G. Zocher, N. Arnberg, 2022, RSC advances.

Isolation and Characterization of Anti-Adenoviral Secondary Metabolites from Marine Actinobacteria

N. Willassen, G. Wadell, M. Elofsson, 2014, Marine drugs.

2-[4,5-Difluoro-2-(2-Fluorobenzoylamino)-Benzoylamino]Benzoic Acid, an Antiviral Compound with Activity against Acyclovir-Resistant Isolates of Herpes Simplex Virus Types 1 and 2

T. Bergström, G. Wadell, M. Elofsson, 2012, Antimicrobial Agents and Chemotherapy.

Identification of Inhibitors of Pseudomonas aeruginosa Exotoxin-S ADP-Ribosyltransferase Activity

H. Schüler, M. Elofsson, A. F. Pinto, 2016, Journal of biomolecular screening.

Pre-clinical pharmacokinetics and anti-chlamydial activity of salicylidene acylhydrazide inhibitors of bacterial type III secretion

Markus K. Dahlgren, Anatoly V. Slepenkin, E. Peterson, 2012, The Journal of Antibiotics.

Chemical probes to study ADP-ribosylation: synthesis and biochemical evaluation of inhibitors of the human ADP-ribosyltransferase ARTD3/PARP3.

C. D. Andersson, A. Linusson, J. Weigelt, 2013, Journal of medicinal chemistry.

Identification of Poly(ADP-Ribose) Polymerase Macrodomain Inhibitors Using an AlphaScreen Protocol

T. Ekblad, H. Schüler, A. Lindgren, 2018, SLAS discovery : advancing life sciences R & D.

PARP3, a new therapeutic target to alter Rictor/mTORC2 signaling and tumor progression in BRCA1-associated cancers

V. Schreiber, A. Tissier, I. Robert, 2018, Cell Death & Differentiation.

Attenuation of Pseudomonas aeruginosa infection by INP0341, a salicylidene acylhydrazide, in a murine model of keratitis

M. Elofsson, Sanhita Roy, P. Sharma, 2020, Virulence.

Synthesis of a water-soluble serine-based neoglycolipid which can be covalently linked to solid phases.

J. Kihlberg, M. Elofsson, J. Broddefalk, 1994, Carbohydrate research.

Glycosylation of C-unprotected 3-mercaptopropionic acid and Fmoc amino acids: Application to the synthesis of glycosylated derivatives of a helper T-cell-stimulating peptide

J. Kihlberg, M. Elofsson, B. Walse, 1993 .

Synthesis and Application of a 2-[(4-Fluorophenyl)-sulfonyl]ethoxy Carbonyl (Fsec) Protected Glycosyl Donor in Carbohydrate Chemistry

S. Spjut, M. Elofsson, W. Qian, 2010, Molecules.

Expression, purification, crystallization and initial X-ray diffraction analysis of thiol peroxidase from Yersinia pseudotuberculosis.

N. Isaacs, M. Gabrielsen, A. Roe, 2010, Acta Crystallographica. Section F : Structural Biology and Crystallization Communications.

Preparation and structural characterization of N-glycated amino acid and linear or cyclic dipeptides containing the 6-amino-6-deoxy-1,2:3,4-di-O-isopropylidene-α--galactopyranose moiety

Š. Horvat, J. Kihlberg, M. Cudic, 1996 .

Loading of the Antigen‐Presenting Protein CD1d with Synthetic Glycolipids

A. Moliner, M. Elofsson, M. Jondal, 2004, Chembiochem : a European journal of chemical biology.

Reversal of the Antichlamydial Activity of Putative Type III Secretion Inhibitors by Iron

Anatoly V. Slepenkin, E. Peterson, L. M. de la Maza, 2007, Infection and Immunity.

Red Fluorescent Chlamydia trachomatis Applied to Live Cell Imaging and Screening for Antibacterial Agents

W. Bahnan, Rohan A. Davis, M. Elofsson, 2018, Front. Microbiol..

Explorer Inhibition of type III secretion in Salmonella enterica serovar typhimurium by small-molecule inhibitors

M. Stevens, H. Wolf‐Watz, M. Elofsson, 2017 .

Preliminary pharmacokinetics of the bacterial virulence inhibitor n'-(3,5-dibromo-2-hydroxy-benzylidenene)-nicotinic Acid hydrazide.

M. Elofsson, Å. Gylfe, A. Blomgren, 2012, Advances in experimental medicine and biology.

Pseudoceramines A-D, new antibacterial bromotyrosine alkaloids from the marine sponge Pseudoceratina sp.

V. Avery, R. Quinn, Rohan A. Davis, 2011, Organic & biomolecular chemistry.

Synthesis of 4‐Formyl‐2‐arylbenzofuran Derivatives by PdCl(C3H5)dppb‐Catalyzed Tandem Sonogashira Coupling‐Cyclization under Microwave Irradiation ‐ Application to the Synthesis of Viniferifuran Analogues

M. Elofsson, Duy Duc Vo, D. D. Vo, 2017 .

Synthesis of Indole-, Benzo[ b]thiophene-, and Benzo[ b]selenophene-Based Analogues of the Resveratrol Dimers Viniferifuran and (±)-Dehydroampelopsin B.

M. Elofsson, Michael Saleeb, A. Krzyzanowski, 2018, Organic letters.

A carbohydrate antigen linked to a T-cell immunogenic peptide induces T-cell clones selective for carbohydrate

E. Unanue, J. Kihlberg, C. Harding, 1993 .

Synthesis and evaluation of 2-(2-fluoro-4-hydroxymethyl-5-methoxy-phenoxy)acetic acid as a linker in solid-phase synthesis monitored by gel-phase 19F NMR spectroscopy

D. Boström, S. Spjut, M. Elofsson, 2007 .

Diversity-Oriented Synthesis of Libraries Based on Benzofuran and 2,3-Dihydrobenzofuran Scaffolds.

C. D. Andersson, D. Vo, M. Elofsson, 2017, ACS combinatorial science.

Synthesis, biological evaluation, and structure-activity relationships of 2-[2-(benzoylamino)benzoylamino]benzoic acid analogues as inhibitors of adenovirus replication.

G. Wadell, M. Elofsson, K. Edlund, 2012, Journal of medicinal chemistry.

Epoxomicin, a potent and selective proteasome inhibitor, exhibits in vivo antiinflammatory activity.

C. Crews, B. Kwok, M. Elofsson, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Statistical molecular design of a focused salicylidene acylhydrazide library and multivariate QSAR of inhibition of type III secretion in the Gram-negative bacterium Yersinia.

Anna Linusson, Markus K. Dahlgren, Mikael Elofsson, 2010, Bioorganic & medicinal chemistry.

The anti-inflammatory natural product parthenolide from the medicinal herb Feverfew directly binds to and inhibits IkappaB kinase.

M Elofsson, C. Crews, B. Kwok, 2001, Chemistry & biology.

Total synthesis of the potent proteasome inhibitor epoxomicin: a useful tool for understanding proteasome biology.

C. Crews, B. Kwok, M. Elofsson, 1999, Bioorganic & medicinal chemistry letters.

Natural product inspired library synthesis - Identification of 2,3-diarylbenzofuran and 2,3-dihydrobenzofuran based inhibitors of Chlamydia trachomatis.

C. D. Andersson, M. Elofsson, Å. Gylfe, 2018, European journal of medicinal chemistry.

Solid-phase synthesis of alpha-Gal epitopes: on-resin analysis of solid-phase oligosaccharide synthesis with 19F NMR spectroscopy.

J. Kihlberg, M. Elofsson, M. Mogemark, 2003, The Journal of organic chemistry.

Preparation of Tn and sialyl Tn building blocks used in Fmoc solid-phase synthesis of glycopeptide fragments from HIV gp120

J. Kihlberg, M. Elofsson, L. A. Salvador, 1997 .

Design, synthesis and evaluation of novel polypharmacological antichlamydial agents.

M. Elofsson, Å. Gylfe, N. Sunduru, 2015, European journal of medicinal chemistry.

Synthesis of Tn and sialyl Tn building blocks for solid phase glycopeptide synthesis

J. Kihlberg, M. Elofsson, 1995 .

Solid‐Phase Synthesis of Glycopeptides: Immunological Studies with T Cell Stimulating Glycopeptides

J. Kihlberg, M. Elofsson, 1997 .

Syntheses of pseudoceramines A-D and a new synthesis of spermatinamine, bromotyrosine natural products from marine sponges.

M. Elofsson, Christopher T Oberg, J. Hillgren, 2012, Organic & biomolecular chemistry.

Total Synthesis of the Resveratrol Oligomers (±)‐Ampelopsin B and (±)‐ϵ‐Viniferin

A. Lindgren, M. Elofsson, Anders E. G. Lindgren, 2015, European Journal of Organic Chemistry.

Small-Molecule Screening Using a Whole-Cell Viral Replication Reporter Gene Assay Identifies 2-{[2-(Benzoylamino)Benzoyl]Amino}-Benzoic Acid as a Novel Antiadenoviral Compound

G. Wadell, S. Spjut, M. Elofsson, 2010, Antimicrobial Agents and Chemotherapy.

Synthesis of 4-O-Alkylated N-Acetylneuraminic Acid Derivatives

M. Elofsson, E. Johansson, Rémi Caraballo, 2020, The Journal of organic chemistry.

Benzylidene Acylhydrazides Inhibit Chlamydial Growth in a Type III Secretion- and Iron Chelation-Independent Manner

H. Fan, H. Caldwell, Gail L. Sturdevant, 2014, Journal of bacteriology.

Exploring resveratrol dimers as virulence blocking agents – Attenuation of type III secretion in Yersinia pseudotuberculosis and Pseudomonas aeruginosa

R. Brkljača, D. Vo, S. Urban, 2020, Scientific Reports.

Triazole linker-based trivalent sialic acid inhibitors of adenovirus type 37 infection of human corneal epithelial cells.

T. Stehle, N. Chandra, N. Arnberg, 2015, Organic & biomolecular chemistry.

Derivatization Procedures for Reducing Oligosaccharides, Part 3: Preparation of Oligosaccharide Glycosylamines, and Their Conversion Into Glycosaccharide - Acrylamide Copolymers

M. Elofsson, T. Norberg, E. Kallin, 1989 .

Synthesis of glycosylated amino acids. Solid-phase assembly of T-cell immunogenic glycopeptides and fragments from HIV gp120

M. Elofsson, 1996 .

Application of gel‐phase 19F NMR spectroscopy for optimization of solid‐phase synthesis of a hydrophobic peptide from the signal sequence of the mucin MUC1

J. Kihlberg, M. Elofsson, Maciej Pudelko, 2007, Journal of peptide science : an official publication of the European Peptide Society.

Carbamate Linker Strategy in Solid-Phase Synthesis of Amino-Functionalized Glycoconjugates for Attachment to Solid Surfaces and Investigation of Protein-Carbohydrate Interactions

S. Spjut, M. Elofsson, Mirja Hartmann, 2009 .

A fluorinated selenide linker for solid-phase synthesis of n-pentenyl glycosides.

J. Kihlberg, M. Elofsson, Christoffer Bengtsson, 2004, Organic letters.

Gel-phase 19F NMR spectral quality for resins commonly used in solid-phase organic synthesis; a study of peptide solid-phase glycosylations.

J. Kihlberg, M. Elofsson, M. Mogemark, 2004, Organic & biomolecular chemistry.

Fluorinated Protective Groups for On‐Resin Quantification of Solid‐Phase Oligosaccharide Synthesis with 19F NMR Spectroscopy

J. Kihlberg, M. Elofsson, M. Mogemark, 2002, Chembiochem : a European journal of chemical biology.

Monitoring solid-phase glycoside synthesis with (19)F NMR spectroscopy.

J. Kihlberg, M. Elofsson, M. Mogemark, 2001, Organic letters.

Dibenzocyclooctadiene lignans from Schisandra spp. selectively inhibit the growth of the intracellular bacteria Chlamydia pneumoniae and Chlamydia trachomatis

E. Hakala, P. Vuorela, H. Vuorela, 2015, The Journal of Antibiotics.

N-Acylated Derivatives of Sulfamethoxazole and Sulfafurazole Inhibit Intracellular Growth of Chlamydia trachomatis

A. Lindgren, M. Elofsson, Hanna Uvell, 2014, Antimicrobial Agents and Chemotherapy.

Cyclopropylmethyl Protection of Phenols: Total Synthesis of the Resveratrol Dimers Anigopreissin A and Resveratrol–Piceatannol Hybrid

M. Elofsson, Michael Saleeb, Arvind Kumar, 2018, ChemistryOpen.

Total Synthesis of Viniferifuran, Resveratrol‐Piceatannol Hybrid, Anigopreissin A and Analogues – Investigation of Demethylation Strategies

D. Vo, M. Elofsson, 2016, Advanced synthesis & catalysis.

Small-Molecule Inhibitors Specifically Targeting Type III Secretion

H. Wolf‐Watz, M. Elofsson, R. Nordfelth, 2005, Infection and Immunity.

Targeting bacterial virulence: inhibitors of type III secretion in Yersinia.

Hans Wolf-Watz, Mikael Elofsson, H. Wolf‐Watz, 2003, Chemistry & biology.

Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme.

J. Kihlberg, M. Elofsson, B. Walse, 1993, Carbohydrate research.

Anti-Rift Valley fever virus activity in vitro, pre-clinical pharmacokinetics and oral bioavailability of benzavir-2, a broad-acting antiviral compound

P. Artursson, M. Evander, C. Ahlm, 2018, Scientific Reports.

PARP3, a new therapeutic target to alter Rictor/mTORC2 signaling and tumor progression in BRCA1-associated cancers

V. Schreiber, A. Tissier, I. Robert, 2018, Cell Death & Differentiation.

PARP inhibitor with selectivity toward ADP-ribosyltransferase ARTD3/PARP3.

Sara Spjut, Anna Linusson, Mikael Elofsson, 2013, ACS chemical biology.

Towards small molecule inhibitors of mono-ADP-ribosyltransferases.

Sara Spjut, Anna Linusson, Mikael Elofsson, 2015, European journal of medicinal chemistry.

Derivatives of 8-hydroxyquinoline--antibacterial agents that target intra- and extracellular Gram-negative pathogens.

M. Elofsson, Å. Gylfe, Per-Anders Enquist, 2012, Bioorganic & medicinal chemistry letters.

Mutations in hemG Mediate Resistance to Salicylidene Acylhydrazides, Demonstrating a Novel Link between Protoporphyrinogen Oxidase (HemG) and Chlamydia trachomatis Infectivity

S. Bergström, R. Bastidas, R. Valdivia, 2013, Journal of bacteriology.

Design of a General‐Purpose European Compound Screening Library for EU‐OPENSCREEN

Dragos Horvath, Gilles Marcou, Jordi Mestres, 2014, ChemMedChem.

Inhibition of Type III Secretion in Salmonella enterica Serovar Typhimurium by Small-Molecule Inhibitors

Edouard E Galyov, Abigail N Layton, Debra L Hudson, 2007, Antimicrobial Agents and Chemotherapy.

Synthesis and application of N‐[1‐(4‐(4‐fluorophenyl)‐2,6‐dioxocyclohexylidene)ethyl] (Fde)‐protected amino acids for optimization of solid‐phase peptide synthesis using gel‐phase 19F NMR spectroscopy

M. Elofsson, W. Qian, Maciej Pudelko, 2009, Journal of peptide science : an official publication of the European Peptide Society.

Identification of a small molecule that stabilizes lipoprotein lipase in vitro and lowers triglycerides in vivo.

G. Olivecrona, M. Elofsson, A. Lõokene, 2014, Biochemical and biophysical research communications.

Crystal structures of WrbA, a spurious target of the salicylidene acylhydrazide inhibitors of type III secretion in Gram-negative pathogens, and verification of improved specificity of next-generation compounds.

M. Gabrielsen, A. Roe, M. Elofsson, 2022, Microbiology.

Design, synthesis, and evaluation of N-acyl modified sialic acids as inhibitors of adenoviruses causing epidemic keratoconjunctivitis.

S. Cusack, D. Guilligay, N. Arnberg, 2009, Journal of medicinal chemistry.

Synthesis and cis–trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues

Š. Horvat, J. Kihlberg, M. Cudic, 1998 .

Statistical molecular design of balanced compound libraries for QSAR modeling.

Markus K. Dahlgren, Ida E. Andersson, A Linusson, 2010, Current medicinal chemistry.

Exploring the Effect of Structure-Based Scaffold Hopping on the Inhibition of Coxsackievirus A24v Transduction by Pentavalent N-Acetylneuraminic Acid Conjugates

C. D. Andersson, N. Ranson, T. Stehle, 2021, International journal of molecular sciences.

Screening for Inhibition of Vibrio cholerae VipA-VipB Interaction Identifies Small-Molecule Compounds Active against Type VI Secretion

A. Sjöstedt, C. D. Andersson, K. Sun, 2014, Antimicrobial Agents and Chemotherapy.

Mycobacterium tuberculosis virulence inhibitors discovered by Mycobacterium marinum high-throughput screening

R. Ummanni, M. Elofsson, Christer Larsson, 2019, Scientific Reports.

Structural Characterisation of Tpx from Yersinia pseudotuberculosis Reveals Insights into the Binding of Salicylidene Acylhydrazide Compounds

Rommie E. Amaro, S. Müller, R. Amaro, 2012, PloS one.

Structure-activity relationships for lipoprotein lipase agonists that lower plasma triglycerides in vivo.

P. Artursson, G. Olivecrona, Valeria Saar, 2015, European journal of medicinal chemistry.

14-3-3 proteins activate Pseudomonas exotoxins-S and -T by chaperoning a hydrophobic surface

E. M. De La Cruz, Elinor Löverli, H. Schüler, 2018, Nature Communications.

Screening for Inhibitors of Acetaldehyde Dehydrogenase (AdhE) from Enterohemorrhagic Escherichia coli (EHEC)

C. Grundström, M. Elofsson, C. Zetterström, 2018, SLAS discovery : advancing life sciences R & D.

14-3-3 proteins activate Pseudomonas exotoxins-S and -T by chaperoning a hydrophobic surface

E. M. De La Cruz, Elinor Löverli, H. Schüler, 2018, Nature Communications.

The gallium(III)-salicylidene acylhydrazide complex shows synergistic anti-biofilm effect and inhibits toxin production by Pseudomonas aeruginosa.

B. Ekstrand-Hammarström, A. Bucht, Shoghik Hakobyan, 2014, Journal of inorganic biochemistry.

Small molecule screening for inhibitors of the YopH phosphatase of Yersinia pseudotuberculosis.

U. Sauer, H. Wolf‐Watz, C. Grundström, 2012, Advances in experimental medicine and biology.

The salicylidene acylhydrazide INP0341 attenuates Pseudomonas aeruginosa virulence in vitro and in vivo

M. Elofsson, Ulrik Hägglund, Charlotta Sundin, 2017, The Journal of Antibiotics.

N-aryl 2-aryloxyacetamides as a new class of fatty acid amide hydrolase (FAAH) inhibitors

C. D. Andersson, M. Svensson, C. Fowler, 2017, Journal of enzyme inhibition and medicinal chemistry.

Development, Optimization, and Validation of a High Throughput Screening Assay for Identification of Tat and Type II Secretion Inhibitors of Pseudomonas aeruginosa

Tuğrul Doruk, M. Elofsson, A. Forsberg, 2019, Front. Cell. Infect. Microbiol..

Salicylanilides are potent inhibitors of type III secretion in Yersinia.

H. Wolf‐Watz, M. Elofsson, R. Nordfelth, 2003, Advances in experimental medicine and biology.

Characterization of a novel mammalian phosphatase having sequence similarity to Schizosaccharomyces pombe PHO2 and Saccharomyces cerevisiae PHO13.

C. Crews, B. Kwok, M. Elofsson, 2002, Biochemistry.

Characterization of the Effects of Salicylidene Acylhydrazide Compounds on Type III Secretion in Escherichia coli O157:H7

M. Stevens, J. Tree, A. Roe, 2009 .

14-3-3 proteins activate Pseudomonas exotoxins-S and -T by chaperoning a hydrophobic surface

E. M. De La Cruz, Elinor Löverli, H. Schüler, 2018, Nature Communications.

Sialic Acid as a Biomarker Studied in Breast Cancer Cell Lines In Vitro Using Fluorescent Molecularly Imprinted Polymers

B. Sellergren, Sudhirkumar Shinde, J. Persson, 2021, Applied Sciences.

Towards subunit-specific proteasome inhibitors: synthesis and evaluation of peptide alpha',beta'-epoxyketones.

C. Crews, U. Splittgerber, M. Elofsson, 1999, Chemistry & biology.