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A Structure‐Activity Investigation of the Fungal Metabolite (−)‐TAN‐2483B: Inhibition of Bruton's Tyrosine Kinase

Chemistry : a European journal, 2024-06, Vol.30 (35), p.e202401051-n/a

2024

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Gadolinium Complexes Attached to Poly Ethoxy Ethyl Glycinamide (PEE‐G) Dendrons: Magnetic Resonance Imaging Contrast Agents with Increased Relaxivity

ChemPlusChem (Weinheim, Germany), 2020-08, Vol.85 (8), p.1881-1892

2020

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The Synthesis and Anti‐tumour Properties of Poly Ethoxy Ethyl Glycinamide (PEE−G) Scaffolds with Multiple PD‐1 Peptides Attached

ChemMedChem, 2020-07, Vol.15 (13), p.1128-1138

2020

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Synthesis of Bioactive Side‐Chain Analogues of TAN‐2483B

Chemistry, an Asian journal, 2019-04, Vol.14 (8), p.1230-1237

2019

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Cytoskeletal alterations that confer resistance to anti-tubulin chemotherapeutics

Anti-cancer agents in medicinal chemistry, 2013-01, Vol.13 (1), p.147-158

2013

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The Big Picture of Glioblastoma Malignancy: A Meta-Analysis of Glioblastoma Proteomics to Identify Altered Biological Pathways

ACS omega, 2021-09, Vol.6 (38), p.24535-24544

2021

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Surprisingly long body length of the lungworm Parafilaroides gymnurus from common seals of the Dutch North Sea

Parasitology research (1987), 2020-06, Vol.119 (6), p.1803-1817

2020

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Total Synthesis of Aigialomycin D Using a Ramberg-Bäcklund/ RCM Strategy

Journal of organic chemistry, 2009-03, Vol.74 (6), p.2271-2277

2009

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BCL6 is a context-dependent mediator of the glioblastoma response to irradiation therapy

International journal of biological macromolecules, 2024-06, Vol.270 (Pt 1), p.131782, Article 131782

2024

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Identification and characterization of protein interactions with the major Niemann–Pick type C disease protein in yeast reveals pathways of therapeutic potential

Genetics (Austin), 2023-08, Vol.225 (1)

2023

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Mechanistic Studies on the Base-Promoted Ring Opening of Glycal-Derived gem-Dibromocyclopropanes

Journal of organic chemistry, 2022-01, Vol.87 (1), p.301-315

2022

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Synthesis of DNA-Directed Pyrrolidinyl and Piperidinyl Confined Alkylating Chloroalkylaminoanthraquinones: Potential for Development of Tumor-Selective N-Oxides

Journal of medicinal chemistry, 2006-11, Vol.49 (24), p.7013-7023

2006

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Characterisation of the biological response of Saccharomyces cerevisiae to the loss of an allele of the eukaryotic initiation factor 4A

Biochemical and biophysical research communications, 2018-02, Vol.496 (4), p.1082-1087

2018

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The protein synthesis inhibitors mycalamides A and E have limited susceptibility toward the drug efflux network

Journal of biochemical and molecular toxicology, 2012-03, Vol.26 (3), p.94-100

2012

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βI-tubulin mutations in the laulimalide/peloruside binding site mediate drug sensitivity by altering drug–tubulin interactions and microtubule stability

Cancer letters, 2015-09, Vol.365 (2), p.251-260

2015

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Synthesis of a simplified triazole analogue of pateamine A

Organic & biomolecular chemistry, 2016-06, Vol.14 (22), p.5117-5127

2016

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Inhibition of glutathione S-transferases (GSTs) from parasitic nematodes by extracts from traditional Nigerian medicinal plants

Phytotherapy research, 2000-12, Vol.14 (8), p.630-634

2000

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Synthesis of mycothiol conjugate analogues and evaluation of their antimycobacterial activity

Bioorganic & medicinal chemistry letters, 2015-05, Vol.25 (10), p.2152-2155

2015

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Towards a simplified peloruside A: synthesis of C1–C11 of a dihydropyran analogue

Tetrahedron, 2011-12, Vol.67 (48), p.9376-9381

2011

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Alkenylphosphonates: unexpected products from reactions of methyl 2-[(diethoxyphosphoryl)methyl]benzoate under Horner-Wadsworth-Emmons conditions

Organic & biomolecular chemistry, 2011-06, Vol.9 (12), p.4432-4435

2011

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A single WW domain is the predominant mediator of the interaction between the human ubiquitin-protein ligase Nedd4 and the human epithelial sodium channel

Biochemical journal, 2002-02, Vol.361 (Pt 3), p.481-488

2002

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The Cellular Target Specificity of Pateamine A

Zeitschrift für Naturforschung C. A journal of biosciences, 2013-09, Vol.68 (9), p.406-415

2013

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Characterizing the laulimalide-peloruside binding site using site-directed mutagenesis of TUB2 in S. cerevisiae

Molecular bioSystems, 2014-01, Vol.10 (1), p.110-116

2014

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A common class of nematode glutathione S-transferase (GST) revealed by the theoretical proteome of the model organism Caenorhabditis elegans

Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 2001-04, Vol.128 (4), p.701-708

2001

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Absence of immunohistochemical evidence for human herpesvirus 8 (HHV8) in oral cavity plasmablastic lymphoma in an HIV-positive man

Clinical oncology (Royal College of Radiologists (Great Britain)), 2000, Vol.12 (3), p.194

2000

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A Structure‐Activity Investigation of the Fungal Metabolite (−)‐TAN‐2483B: Inhibition of Bruton's Tyrosine Kinase

Gadolinium Complexes Attached to Poly Ethoxy Ethyl Glycinamide (PEE‐G) Dendrons: Magnetic Resonance Imaging Contrast Agents with Increased Relaxivity

The Synthesis and Anti‐tumour Properties of Poly Ethoxy Ethyl Glycinamide (PEE−G) Scaffolds with Multiple PD‐1 Peptides Attached

Synthesis of Bioactive Side‐Chain Analogues of TAN‐2483B

Cytoskeletal alterations that confer resistance to anti-tubulin chemotherapeutics

The Big Picture of Glioblastoma Malignancy: A Meta-Analysis of Glioblastoma Proteomics to Identify Altered Biological Pathways

Surprisingly long body length of the lungworm Parafilaroides gymnurus from common seals of the Dutch North Sea

Total Synthesis of Aigialomycin D Using a Ramberg-Bäcklund/ RCM Strategy

BCL6 is a context-dependent mediator of the glioblastoma response to irradiation therapy

Identification and characterization of protein interactions with the major Niemann–Pick type C disease protein in yeast reveals pathways of therapeutic potential

Mechanistic Studies on the Base-Promoted Ring Opening of Glycal-Derived gem-Dibromocyclopropanes

Synthesis of DNA-Directed Pyrrolidinyl and Piperidinyl Confined Alkylating Chloroalkylaminoanthraquinones: Potential for Development of Tumor-Selective N-Oxides

Characterisation of the biological response of Saccharomyces cerevisiae to the loss of an allele of the eukaryotic initiation factor 4A

The protein synthesis inhibitors mycalamides A and E have limited susceptibility toward the drug efflux network

βI-tubulin mutations in the laulimalide/peloruside binding site mediate drug sensitivity by altering drug–tubulin interactions and microtubule stability

Synthesis of a simplified triazole analogue of pateamine A

Inhibition of glutathione S-transferases (GSTs) from parasitic nematodes by extracts from traditional Nigerian medicinal plants

Synthesis of mycothiol conjugate analogues and evaluation of their antimycobacterial activity

Towards a simplified peloruside A: synthesis of C1–C11 of a dihydropyran analogue

Alkenylphosphonates: unexpected products from reactions of methyl 2-[(diethoxyphosphoryl)methyl]benzoate under Horner-Wadsworth-Emmons conditions

A single WW domain is the predominant mediator of the interaction between the human ubiquitin-protein ligase Nedd4 and the human epithelial sodium channel

The Cellular Target Specificity of Pateamine A

Characterizing the laulimalide-peloruside binding site using site-directed mutagenesis of TUB2 in S. cerevisiae

A common class of nematode glutathione S-transferase (GST) revealed by the theoretical proteome of the model organism Caenorhabditis elegans

Absence of immunohistochemical evidence for human herpesvirus 8 (HHV8) in oral cavity plasmablastic lymphoma in an HIV-positive man

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