J. Malkinson

发表

T-shaped Peptide Amphiphiles Self Assemble into Nanofiber Networks.

F. Fisusi, R. Notman, Louis A Granger, 2018, Pharmaceutical nanotechnology.

A new plant-derived antibacterial is an inhibitor of efflux pumps in Staphylococcus aureus.

D. Livermore, S. Neidle, M. Gunaratnam, 2013, International journal of antimicrobial agents.

2-Hydroxy-substituted cinnamic acids and acetanilides are selective growth inhibitors of Mycobacterium tuberculosis

J. Malkinson, S. Bhakta, S. Gibbons, 2014 .

Three-Dimensional Printing of a Scalable Molecular Model and Orbital Kit for Organic Chemistry Teaching and Learning

B. Szulc, J. Malkinson, C. Asquith, 2017 .

Efficient solid-phase-based total synthesis of the bisintercalator TANDEM.

Andrew J. Hampshire, M. Zloh, J. Malkinson, 2005, The Journal of organic chemistry.

Bisintercalator natural products with potential therapeutic applications: isolation, structure determination, synthetic and biological studies.

J. Malkinson, M. Searcey, S. Dawson, 2007, Natural product reports.

In Silico Structural Evaluation of Short Cationic Antimicrobial Peptides

M. Zloh, J. Malkinson, S. Rossiter, 2018, Pharmaceutics.

Analogues of Disulfides from Allium stipitatum Demonstrate Potent Anti-tubercular Activities through Drug Efflux Pump and Biofilm Inhibition

J. Malkinson, S. Bhakta, S. Gibbons, 2018, Scientific Reports.

Synthesis and antibacterial evaluation of 3-Farnesyl-2-hydroxybenzoic acid from Piper multiplinervium.

I. Malami, J. Malkinson, S. Gibbons, 2014, Fitoterapia.

LONDON Crowdfunding to Finance R&D of Treatments for Neglected Tropical Diseases: Current Trends in and Future Potential

J. Malkinson, G. Tóth, Safouane M. Benazzouz, 2021 .

Bioactive pyridine-N-oxide disulfides from Allium stipitatum.

Stephen Neidle, Simon Gibbons, Mekala Gunaratnam, 2009, Journal of natural products.

Antibacterial acylphloroglucinols from Hypericum olympicum.

M. Zloh, J. Malkinson, M. M. Rahman, 2012, Journal of natural products.

Antitubercular specific activity of ibuprofen and the other 2-arylpropanoic acids using the HT-SPOTi whole-cell phenotypic assay

S. Mwaigwisya, J. Malkinson, S. Bhakta, 2013, BMJ Open.

Synthesis and in Silico Modelling of the Potential Dual Mechanistic Activity of Small Cationic Peptides Potentiating the Antibiotic Novobiocin against Susceptible and Multi-Drug Resistant Escherichia coli

M. Zloh, J. Malkinson, P. Stapleton, 2020, International journal of molecular sciences.

Synthesis of C-terminal glycopeptides from resin-bound glycosyl azides via a modified Staudinger reaction.

I. Toth, J. Malkinson, R. Falconer, 2000, The Journal of organic chemistry.

Solid-phase synthesis of C-terminal thio-linked glycopeptides

J. Malkinson, R. Falconer, 2002 .

Novel lipoamino acid and liposaccharide based peptide delivery system for tumor selective somatostatin analogs

G. Kéri, P. Artursson, I. Toth, 2000 .

Novel lipoamino acid- and liposaccharide-based system for peptide delivery: application for oral administration of tumor-selective somatostatin analogues.

G. Kéri, P. Artursson, L. Lazorova, 1999, Journal of medicinal chemistry.

A new principle for tight junction modulation based on occludin peptides.

P. Artursson, L. Lazorova, I. Toth, 2003, Molecular pharmacology.

Current trends in, and future potential of, crowdfunding to finance R&D of treatments for neglected tropical diseases.

G. Tóth, J. Malkinson, Safouane M. Benazzouz, 2021, Drug discovery today.

A prodrug nanoparticle approach for the oral delivery of a hydrophilic peptide, leucine(5)-enkephalin, to the brain.

A. Schätzlein, M. Zloh, J. Malkinson, 2012, Molecular pharmaceutics.

Solid-phase synthesis of the cyclic peptide portion of chlorofusin, an inhibitor of p53-MDM2 interactions.

M. Zloh, R. Errington, J. Malkinson, 2003, Organic letters.

Solid-phase synthesis of chlorofusin analogues.

J. Malkinson, A. Wilderspin, E. Woon, 2007, The Journal of organic chemistry.

In Silico Structural Evaluation of Short Cationic Antimicrobial Peptides

M. Zloh, J. Malkinson, S. Rossiter, 2018, Pharmaceutics.