Search results (642)
« Back to PublicationsLead optimisation of OXS007417: in vivo PK profile and hERG liability modulation to optimise a small molecule differentiation agent for the potential treatment of acute myeloid leukaemia.
Journal article
Cogswell TJ. et al, (2024), RSC Med Chem, 15, 3495 - 3506
β-Peptides incorporating polyhydroxylated cyclohexane β-amino acid: synthesis and conformational study.
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Reza D. et al, (2023), Org Biomol Chem, 21, 8535 - 8547
General Approach to Enantiopure 1-Aminopyrrolizidines: Application to the Asymmetric Synthesis of the Loline Alkaloids.
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Davies SG. et al, (2023), J Org Chem, 88, 8093 - 8098
Microgrewiapine C: Asymmetric Synthesis, Spectroscopic Data, and Configuration Assignment.
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Davies SG. et al, (2022), J Nat Prod, 85, 1872 - 1879
Synthesis and Configuration of O-Acetyl Microgrewiapine A: Phantomization of O-Acetyl 6-epi-Microgrewiapine A.
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Davies SG. et al, (2022), J Nat Prod, 85, 306 - 312
A phenotypic screen identifies a compound series that induces differentiation of acute myeloid leukemia cells in vitro and shows antitumor effects in vivo
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Josa-Culleré L. et al, (2021), Journal of Medicinal Chemistry
Mutual kinetic resolution: probing enantiorecognition phenomena and screening for kinetic resolution with racemic reagents.
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Davies SG. et al, (2021), Org Biomol Chem, 19, 2847 - 2855
Decreasing HepG2 Cytotoxicity by Lowering the Lipophilicity of Benzo[d]oxazolephosphinate Ester Utrophin Modulators.
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Chatzopoulou M. et al, (2020), ACS Med Chem Lett, 11, 2421 - 2427
2-Arylbenzo[d]oxazole Phosphinate Esters as Second-Generation Modulators of Utrophin for the Treatment of Duchenne Muscular Dystrophy.
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Babbs A. et al, (2020), Journal of medicinal chemistry, 63, 7880 - 7891
Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid.
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Wilkinson IVL. et al, (2020), Angew Chem Int Ed Engl, 59, 2420 - 2428
Synthesis of SMT022357 enantiomers and in vivo evaluation in a Duchenne muscular dystrophy mouse model.
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Babbs A. et al, (2020), Tetrahedron, 76
Asymmetric syntheses of fagomine and its stereoisomers
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Davies SG. et al, (2019), Tetrahedron, 75
The asymmetric synthesis of (S,S)-methylphenidate hydrochloride via ring-opening of an enantiopure aziridinium intermediate with phenylmagnesium bromide
Journal article
Davies SG. et al, (2019), Tetrahedron, 75
Asymmetric synthesis of the allocolchicinoid natural product N-acetylcolchinol methyl ether (suhailamine), solid state and solution phase conformational analysis
Journal article
Davies SG. et al, (2019), Tetrahedron, 75
Isolation, structural identification, synthesis, and pharmacological profiling of 1,2-trans-dihydro-1,2-diol metabolites of the utrophin modulator ezutromid
Journal article
Chatzopoulou M. et al, (2019), Journal of Medicinal Chemistry, 63, 2547 - 2556
