A. Luxenburger

发表

The synthesis of 3-azabicyclo[4.3.0]nonane scaffolds from brefeldin A

N. T. Lucas, Bill C. Hawkins, Brooke E. Swaney, 2020 .

Optimized 4,5-Diarylimidazoles as Potent/Selective Inhibitors of Protein Kinase CK1δ and Their Structural Relation to p38α MAPK

U. Baumann, U. Knippschild, D. Rauh, 2017, Molecules.

'Segmented' crystals solved using synchrotron radiation: (2S,3R,4S,5R)-4-(10,10-dimethyl-3,3-dioxo-3lambda6-thia-4-azatricyclo[5.2.1.0(1,5)]decan-4-ylcarbonyl)-2,6-diphenylperhydropyrrolo[3,4-c]pyrrole-1,3-dione.

G. Gainsford, A. Luxenburger, S. Mee, 2009, Acta crystallographica. Section C, Crystal structure communications.

A high-throughput screen to identify novel synthetic lethal compounds for the treatment of E-cadherin-deficient cells

Bryony J. Telford, P. Guilford, Augustine Chen, 2019, Scientific Reports.

Synthesis and Characterization of Transition-State Analogue Inhibitors against Human DNA Methyltransferase 1.

V. Schramm, P. Tyler, A. D. Woolhouse, 2022, Journal of medicinal chemistry.

Synthesis of Novel C/D Ring Modified Bile Acids

R. Furneaux, B. Compton, Lawrence D. Harris, 2022, Molecules.

Synthesis of 12β-Methyl-18-nor-bile Acids

R. Furneaux, C. Ling, R. Piltz, 2021, ACS omega.

Discovery of AL-GDa62 as a Potential Synthetic Lethal Lead for the Treatment of Gastric Cancer.

G. Evans, Nicola Bougen-Zhukov, P. Guilford, 2021, Journal of medicinal chemistry.

Tight binding enantiomers of pre-clinical drug candidates.

G. Evans, V. Schramm, P. Tyler, 2015, Bioorganic & medicinal chemistry.

A facile synthetic approach to the core structure of 6,7-didehydrocarnosoic acid type derivatives

A. Luxenburger, 2003 .

The synthesis of carnosol derivatives

A. Luxenburger, 2003 .

Mercury(II) Trifluoroacetate

P. Kočovský, A. Luxenburger, 2008 .

Alkali metal counterion control of enolate protonation stereoselectivity.

L. Paquette, A. Luxenburger, Shuzhi Dong, 2006, Organic letters.

Alkyl 4-chlorobenzoyloxycarbamates as highly effective nitrogen source reagents for the base-free, intermolecular aminohydroxylation reaction.

R. Furneaux, G. Gainsford, A. Luxenburger, 2011, The Journal of organic chemistry.

C5‐Iminosugar modification of casein kinase 1δ lead 3‐(4‐fluorophenyl)‐5‐isopropyl‐4‐(pyridin‐4‐yl)isoxazole promotes enhanced inhibitor affinity and selectivity

U. Knippschild, A. D. Woolhouse, C. Peifer, 2022, Archiv der Pharmazie.

Studies toward the total synthesis of dumsin. 2. A second generation approach resulting in enantioselective construction of a functionalized ABC subunit of the tetranortriterpenoid insect antifeedant.

L. Paquette, A. Luxenburger, Raynauld L. Bishop, 2007, The Journal of organic chemistry.

Design, Synthesis and Biological Evaluation of Isoxazole-Based CK1 Inhibitors Modified with Chiral Pyrrolidine Scaffolds

U. Baumann, U. Knippschild, G. Gainsford, 2019, Molecules.

(3R,6S,7aS)-3-Phenyl-6-(phenylsulfanyl)perhydropyrrolo[1,2-c]oxazol-5-one

A. D. Woolhouse, G. Gainsford, A. Luxenburger, 2009, Acta crystallographica. Section E, Structure reports online.

The discovery of 12β-methyl-17-epi-18-nor-bile acids as potent and selective TGR5 agonists.

R. Furneaux, W. Jiao, A. D. Woolhouse, 2023, European journal of medicinal chemistry.

Steady-state and pre-steady-state kinetic analysis of Mycobacterium smegmatis cysteine ligase (MshC).

J. Blanchard, G. Painter, A. Luxenburger, 2007, Biochemistry.

3α,7-Dihydroxy-14(13→12)abeo-5β,12α(H),13β(H)-cholan-24-oic Acids Display Neuroprotective Properties in Common Forms of Parkinson’s Disease

R. Furneaux, H. Mortiboys, O. Bandmann, 2022, Biomolecules.

A Facile Synthetic Approach to the Core Structure of 6,7‐Didehydrocarnosoic Acid Type Derivatives.

A. Luxenburger, 2003 .

Characterization of a computerized assay for rapid and easy determination of leukocyte adhesion to endothelial cells.

A. Luxenburger, G. Dannhardt, H. Ulbrich, 2005, Biological & pharmaceutical bulletin.

(2S,3R,4S,5R)-Diethyl 2-(10,10-dimethyl-3,3-dioxo-3lambda(6)-thia-4-azatricyclo[5.2.1.0(1,5)]decan-4-ylcarbonyl)-5-phenylpyrrolidine-3,4-dicarboxylate: a novel isomorphous-by-addition compound.

G. Gainsford, A. Luxenburger, S. Mee, 2009, Acta crystallographica. Section C, Crystal structure communications.

A novel class of potent nonglycosidic and nonpeptidic pan-selectin inhibitors.

O. Soehnlein, L. Lindbom, E. Eriksson, 2006, Journal of Medicinal Chemistry.

(9H-Fluoren-9-yl)methyl N-{(2R,3R,4S)-4-hydroxy-2-[(2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-5-oxooxolan-3-yl}carbamate propan-2-ol 0.334-solvate

G. Gainsford, A. Luxenburger, 2012, Acta crystallographica. Section E, Structure reports online.

MedicaLVR: towards medical remote collaboration using virtual reality

Daniel Sonntag, Mohammad Mehdi Moniri, Andreas Luxenburger, 2016, UbiComp Adjunct.

Synthesis of 12β-methyl-18-nor-avicholic acid analogues as potential TGR5 agonists.

R. Furneaux, J. Pitman, A. Luxenburger, 2022, Organic & biomolecular chemistry.