A. Sundin

发表

Highly Diastereoselective Hydrogenations Leading to β-Hydroxy δ-Lactones in Hydroxy-Protected Form. A Modified View of δ-Lactone Conformations

S. Brandänge, M. Färnbäck, H. Leijonmarck, 2003 .

A Remarkably Complex Supramolecular Hydrogen-Bonded Decameric Capsule Formed from an Enantiopure C₂-Symmetric Monomer by Solvent-Responsive Aggregation.

K. Wärnmark, Qixun Shi, K. Bergquist, 2015, Journal of the American Chemical Society.

Double affinity amplification of galectin-ligand interactions through arginine-arene interactions: synthetic, thermodynamic, and computational studies with aromatic diamido thiodigalactosides.

U. Nilsson, H. Leffler, I. Cumpstey, 2008, Chemistry.

Iridium catalyzed carbocyclizations: efficient (5+2) cycloadditions of vinylcyclopropanes and alkynes.

D. Strand, M. Melcher, A. Sundin, 2015, Chemistry.

1H-1,2,3-triazol-1-yl thiodigalactoside derivatives as high affinity galectin-3 inhibitors.

U. Nilsson, H. Leffler, B. Salameh, 2010, Bioorganic & medicinal chemistry.

Thioureido N-acetyllactosamine derivatives as potent galectin-7 and 9N inhibitors.

U. Nilsson, H. Leffler, B. Salameh, 2006, Bioorganic & medicinal chemistry.

Affinity of galectin-8 and its carbohydrate recognition domains for ligands in solution and at the cell surface.

R. Cummings, A. Karlsson, U. Nilsson, 2007, Glycobiology.

Cobalt-mediated solid phase synthesis of 3-O-alkynylbenzyl galactosides and their evaluation as galectin inhibitors

N. Kann, U. Nilsson, H. Leffler, 2006 .

Rules for priming and inhibition of glycosaminoglycan biosynthesis; probing the beta 4GalT7 active site

K. Mani, G. Widmalm, G. Westergren-Thorsson, 2014 .

The structure of human dermatan sulfate epimerase 1 emphasizes the importance of C5-epimerization of glucuronic acid in higher organisms

Lars Malmström, Hamed Khakzad, J. Malmström, 2020, Chemical science.

Quinoline-galactose hybrids bind selectively with high affinity to a galectin-8 N-terminal domain.

S. Oredsson, S. Persson, Mukul Mahanti, 2018, Organic & biomolecular chemistry.

Synthetic receptor analogues: preparation and calculated conformations of the 2-deoxy, 6-O-methyl, 6-deoxy, and 6-deoxy-6-fluoro derivatives of methyl 4-O-α-d-galactopyranosyl-β-d-galactopyranoside (methyl β-d-galabioside)☆

J. Kihlberg, G. Magnusson, T. Frejd, 1988 .

Studies of Arginine–Arene Interactions through Synthesis and Evaluation of a Series of Galectin‐Binding Aromatic Lactose Esters

U. Nilsson, H. Leffler, I. Cumpstey, 2007, Chembiochem : a European journal of chemical biology.

Paracetamol analogues conjugated by FAAH induce TRPV1-mediated antinociception without causing acute liver toxicity.

A. Eschalier, A. Blomqvist, K. Shionoya, 2020, European journal of medicinal chemistry.

Haemophilus influenzae surface fibril (Hsf) is a unique twisted hairpin-like trimeric autotransporter.

K. Riesbeck, S. Linse, M. Mörgelin, 2015, International journal of medical microbiology : IJMM.

The binding mechanism of the virulence factor Streptococcus suis adhesin P subtype to globotetraosylceramide is associated with systemic disease

J. Corander, T. Nyholm, A. Papageorgiou, 2020, The Journal of Biological Chemistry.

The binding mechanism of Streptococcus suis accessory virulence factor and adhesin SadP to globotetraosylceramide

J. Corander, T. Nyholm, A. Papageorgiou, 2020, bioRxiv.

Synthesis of chiral, amphiphilic, and water-soluble macrocycles via urea formation

U. Nilsson, A. Sundin, T. Bhattacharyya, 2003 .

Furanocembranoid Diterpenes as Defensive Compounds in the Dufour Gland of the Ant Crematogaster brevispinosa rochai

J. Braekman, D. Daloze, J. Pasteels, 2000 .

A Unifying Bioinspired Synthesis of (−)-Asperaculin A and (−)-Penifulvin D

D. Strand, A. Sundin, Miguel López-Tena, 2021, Organic Letters.

Carbohydrate-derived chiral furanosidic α,β-unsaturated aldehydes in conjugate and Diels-Alder addition reactions. Steric hindrance by the anomeric substituent

N. Rehnberg, A. Sundin, G. Magnusson, 1990 .

Asymmetric diels-alder reaction between the chiral isoprene units 2-(r)-and (s)-benzyloxy-2,5-dihydro-4-furancarboxaldehyde and cyclopentadiene

T. Frejd, A. Sundin, G. Magnusson, 1985 .

Synthesis of Substituted Oxazoles from N‐Benzyl Propargyl Amines and Acid Chlorides

D. Strand, A. Sundin, F. Paulsen, 2013 .

Structure-Guided Design of d-Galactal Derivatives with High Affinity and Selectivity for the Galectin-8 N-Terminal Domain

M. Anderluh, T. Tomašič, M. Håkansson, 2021, ACS medicinal chemistry letters.

Galactose-amidine derivatives as selective antagonists of galectin-9

U. Nilsson, H. Leffler, B. Mukhopadhyay, 2016 .

Composition- and size-controlled cyclic self-assembly by solvent- and C60-responsive self-sorting.

Mikael Lund, K. Wärnmark, Jilai Li, 2013, Journal of the American Chemical Society.

Formation of an heterochiral supramolecular cage by diastereomer self-discrimination: fluorescence enhancement and C60 sensing.

K. Wärnmark, O. Wendt, R. Lemieux, 2010, Chemical communications.

Monovalent interactions of galectin-1.

J. Rini, Hanna A. Rydberg, Y. Lobsanov, 2010, Biochemistry.

Chiral multifunctional isoprene units by ring-contraction of riboside oxiranes

T. Frejd, A. Sundin, G. Magnusson, 1986 .

Benzimidazole-galactosides bind selectively to the Galectin-8 N-Terminal domain: Structure-based design and optimisation.

M. Anderluh, C. Diehl, T. Tomašič, 2021, European journal of medicinal chemistry.

Mutational Tuning of Galectin-3 Specificity and Biological Function

J. Rini, A. Karlsson, Ruth Hendus-Altenburger, 2010, The Journal of Biological Chemistry.

C2-symmetrical thiodigalactoside bis-benzamido derivatives as high-affinity inhibitors of galectin-3: efficient lectin inhibition through double arginine-arene interactions.

U. Nilsson, H. Leffler, I. Cumpstey, 2005, Angewandte Chemie.

Synthesis of a 3'-naphthamido-LacNAc fluorescein conjugate with high selectivity and affinity for galectin-3.

U. Nilsson, H. Leffler, Johan Tejler, 2006, Carbohydrate research.

Epimers Switch Galectin-9 Domain Selectivity: 3N-Aryl Galactosides Bind the C-Terminal and Gulosides Bind the N-Terminal.

Mukul Mahanti, U. Nilsson, H. Leffler, 2019, ACS medicinal chemistry letters.

Aglycone specificity of Thermotoga neapolitana β-glucosidase 1A modified by mutagenesis, leading to increased catalytic efficiency in quercetin-3-glucoside hydrolysis

Eva Nordberg Karlsson, Sofia Lindahl, Tania Pozzo, 2011, BMC Biochemistry.

Total Synthesis of (−)-Glionitrin A and B Enabled by an Asymmetric Oxidative Sulfenylation of Triketopiperazines

D. Strand, A. Sundin, Nicolas R. Koning, 2021, Journal of the American Chemical Society.

Experimental and Computational Models for Side Chain Discrimination in Peptide–Protein Interactions

K. Wärnmark, P. Norrby, A. Ryberg, 2021, Chemistry.

N-Substituted salicylamides as selective malaria parasite dihydroorotate dehydrogenase inhibitors

G. McConkey, U. Nilsson, Paul T. P. Bedingfield, 2011 .

Diels–Alder adducts derived from the natural phthalide Z-ligustilide

O. Sterner, Erik Lager, R. Toscano, 2007 .

Formation of an heterochiral supramolecular cage by diastereomer self-discrimination: fluorescence enhancement and C60 sensing.

K. Wärnmark, O. Wendt, R. Lemieux, 2010, Chemical communications.

Composition- and size-controlled cyclic self-assembly by solvent- and C60-responsive self-sorting.

Mikael Lund, K. Wärnmark, Jilai Li, 2013, Journal of the American Chemical Society.

Designing interactions by control of protein–ligand complex conformation: tuning arginine–arene interaction geometry for enhanced electrostatic protein–ligand interactions

M. Akke, O. Engström, H. Leffler, 2017, Chemical science.

The structure determination of panellon and panellol, two 14-noreudesmanes isolated from resupinatus leightonii

M. Stadler, H. Anke, O. Sterner, 1993 .

Selective Galectin‐8N Ligands: The Design and Synthesis of Phthalazinone‐d‐Galactals

M. Anderluh, T. Tomašič, U. Nilsson, 2021, ChemMedChem.