New and unusual scaffolds in medicinal chemistry von Marson, Charles M

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Multicomponent and sequential organocatalytic reactions: diversity with atom-economy and enantiocontrol von Marson, Charles M

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Domino Michael-aldol annulations for the stereocontrolled synthesis of bicyclo[3.3.1]nonane and bicyclo[3.2.1]octane derivatives von Promontorio, Rossella, Richard, Jean-Alexandre, Marson, Charles M.

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Thiostrepton selectively targets breast cancer cells through inhibition of forkhead box M1 expression von Kwok, Jimmy M-M, Myatt, Stephen S, Marson, Charles M, Coombes, R Charles, Constantinidou, Demetra, Lam, Eric W-F

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A distal regulatory region of a class I human histone deacetylase von Werbeck, Nicolas D., Shukla, Vaibhav Kumar, Kunze, Micha B. A., Yalinca, Havva, Pritchard, Ruth B., Siemons, Lucas, Mondal, Somnath, Greenwood, Simon O. R., Kirkpatrick, John, Marson, Charles M., Hansen, D. Flemming

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Potent and Selective Inhibitors of Histone Deacetylase‑3 Containing Chiral Oxazoline Capping Groups and a N‑(2-Aminophenyl)-benzamide Binding Unit von Marson, Charles M., Matthews, Christopher J., Atkinson, Stephen J., Lamadema, Nermina, Thomas, N. Shaun B.

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Targeting TAO Kinases Using a New Inhibitor Compound Delays Mitosis and Induces Mitotic Cell Death in Centrosome Amplified Breast Cancer Cells von Koo, Chuay-Yeng, Giacomini, Caterina, Reyes-Corral, Marta, Olmos, Yolanda, Tavares, Ignatius A, Marson, Charles M, Linardopoulos, Spiros, Tutt, Andrew N, Morris, Jonathan D H

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Targeting the Histamine H4 Receptor von Marson, Charles M

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Monocyclic Quinone Structure‐Activity Patterns: Synthesis of Catalytic Inhibitors of Topoisomerase II with Potent Antiproliferative Activity von Waugh, Thomas M., Masters, John, Aliev, Abil E., Marson, Charles M.

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A stepwise lactol carbocyclisation to bridged ethers via a keto–acetal cascade von McCarthy, Sean, Marson, Charles M

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A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones von Marson, Charles M, Edaan, Esra, Morrell, James M, Coles, Simon J, Hursthouse, Michael B, Davies, David T

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Potent non-hydroxamate inhibitors of histone deacetylase-8: Role and scope of an isoindolin-2-yl linker with an α-amino amide as the zinc-binding unit von Greenwood, Simon O.R., Chan, A.W. Edith, Hansen, D. Flemming, Marson, Charles M.

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Synthesis of the penta-oxazole core of telomestatin in a convergent approach to poly-oxazole macrocycles von Marson, Charles M, Saadi, Mona

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Discovery of Potent, Isoform-Selective Inhibitors of Histone Deacetylase Containing Chiral Heterocyclic Capping Groups and a N‑(2-Aminophenyl)benzamide Binding Unit von Marson, Charles M, Matthews, Christopher J, Yiannaki, Elena, Atkinson, Stephen J, Soden, Peter E, Shukla, Lena, Lamadema, Nermina, Thomas, N. Shaun B

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Pteridine-2,4-diamine derivatives as radical scavengers and inhibitors of lipoxygenase that can possess anti-inflammatory properties von Pontiki, Eleni, Hadjipavlou-Litina, Dimitra, Patsilinakos, Alexandros, Tran, Trang M, Marson, Charles M

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Targeting the Histamine H 4 Receptor von Marson, Charles M.

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Production of malodorous steroids from androsta-5,16-dienes and androsta-4,16-dienes by Corynebacteria and other human axillary bacteria von Decréau, Richard A, Marson, Charles M, Smith, Kelvin E, Behan, John M

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Synthesis via N-acyliminium cyclisations of N-heterocyclic ring systems related to alkaloids von Marson, Charles M.

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The histone deacetylase inhibitor UCL67022 has potent activity in multiple myeloma and non‐Hodgkin lymphoma pre‐clinical models von Maharaj, Lenushka, Marson, Charles M., Middleton, Brian J., Rioja, Alf S., Perry, Jackie, Oakervee, Heather, Cavenagh, Jamie, Joel, Simon P., Popat, Rakesh

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Discovery of a structurally novel, drug-like and potent inhibitor of peptidylarginine deiminase von Ferretti, Patrizia, U, Kin Pong, Vagaska, Barbora, Merchant, Rohan, Matthews, Christopher J, Marson, Charles M

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