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Oxidative stress-responsive 1 kinase catalytic activity promotes triple negative breast cancer oncogenic potential.
ACS pharmacology & translational science
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Xu, Qin, Sharif, Maria, James, Edward, Dismorr, Jack O., Tucker, James H. R., Willcox, Benjamin E. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2024.
Phosphonodiamidate prodrugs of phosphoantigens (ProPAgens) exhibit potent Vγ9/Vδ2 T cell activation and eradication of cancer cells †.
RSC Medicinal Chemistry
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10.1039/d4md00208c
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
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Parkinson's disease: are PINK1 activators inching closer to the clinic?
ACS Medicinal Chemistry Letters
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10.1021/acsmedchemlett.3c00070
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Lambourne, Olivia A., Bell, Shane, Wilhelm, Léa P., Yarbrough, Erika B., Holly, Gabriel G., Russell, Oliver M., Alghamdi, Arwa M., Fdel, Azeza M., Varricchio, Carmine ORCID: https://orcid.org/0000-0002-1673-4768, Lane, Emma L. ORCID: https://orcid.org/0000-0001-8800-3764, Ganley, Ian G., Jones, Arwyn T. ORCID: https://orcid.org/0000-0003-2781-8905, Goldberg, Matthew S. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2023.
PINK1-Dependent mitophagy inhibits elevated ubiquitin phosphorylation caused by mitochondrial damage.
Journal of Medicinal Chemistry
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10.1021/acs.jmedchem.3c00555
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Elvers, Karen T., Lipka-Lloyd, Magdalena, Trueman, Rebecca C., Bax, Benjamin D. ORCID: https://orcid.org/0000-0003-1940-3785 and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2022.
Structures of the human SPAK and OSR1 conserved C-terminal (CCT) domains.
ChemBioChem
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10.1002/cbic.202100441
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Alanazi, Ashwag S., Miccoli, Ageo and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2021.
Aryloxy pivaloyloxymethyl prodrugs as nucleoside monophosphate prodrugs.
Journal of Medicinal Chemistry
64
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10.1021/acs.jmedchem.1c01490
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Xu, Qin, Taher, Taher E., Ashby, Elizabeth, Sharif, Maria, Willcox, Benjamin E. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2021.
Generation of stable isopentenyl monophosphate aryloxy triester phosphoramidates as activators of Vγ9Vδ2 T cells.
ChemMedChem
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10.1002/cmdc.202100198
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Elzwawi, Abdulrahman, Grafton, Gillian, Barnes, Nicholas M. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2020.
SPAK and OSR1 kinases bind and phosphorylate the β2-Adrenergic receptor.
Biochemical and Biophysical Research Communications
532
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10.1016/j.bbrc.2020.07.143
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Kadri, Hachemi, Taher, Taher E., Xu, Qin, Sharif, Maria, Ashby, Elizabeth, Bryan, Richard T., Willcox, Benjamin E. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2020.
Aryloxy diester phosphonamidate prodrugs of phosphoantigens (ProPAgens) as potent activators of Vγ9/Vδ2 T-Cell immune responses.
Journal of Medicinal Chemistry
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10.1021/acs.jmedchem.0c01232
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Miccoli, Ageo, Dhiani, Binar A., Thornton, Peter J., Lambourne, Olivia A., James, Edward, Kadri, Hachemi and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2020.
Aryloxy triester phosphoramidates as phosphoserine prodrugs: a proof of concept study.
ChemMedChem
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10.1002/cmdc.202000034
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Dhiani, Binar Asrining and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2020.
The Cul4‐DDB1‐WDR3/WDR6 complex binds SPAK and OSR1 kinases in a phosphorylation‐dependent manner.
ChemBioChem
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10.1002/cbic.201900454
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AlAmri, Mubarak A., Jeeves, Mark and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2019.
Sequence specific assignment and determination of OSR1 C-terminal domain structure by NMR.
Biochemical and Biophysical Research Communications
512
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10.1016/j.bbrc.2019.03.065
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Miccoli, Ageo, Dhiani, Binar and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2019.
Phosphotyrosine prodrugs: design, synthesis and anti-STAT3 activity of ISS-610 aryloxy triester phosphoramidate prodrugs.
MedChemComm
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10.1039/C8MD00244D
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Alanazi, Ashwag S., James, Edward and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2019.
The protide prodrug technology: Where next?
ACS Medicinal Chemistry Letters
10
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10.1021/acsmedchemlett.8b00586
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Lambourne, Olivia A. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2018.
Chemical strategies for activating PINK1, a protein kinase mutated in Parkinson's Disease.
ChemBioChem
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10.1002/cbic.201800497
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AlAmri, Mubarak A, Kadri, Hachemi, Jeeves, Mark, Alderwick, Luke J and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2018.
The photosensitizing clinical agent verteporfin is an inhibitor of SPAK and OSR1 kinases.
ChemBioChem
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10.1002/cbic.201800272
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Alamri, Mubarak A., Dhiani, Binar A. and Kadri, Hachemi
2018.
C -terminal phosphorylation of SPAK and OSR1 kinases promotes their binding and activation by the scaffolding protein MO25.
Biochemical and Biophysical Research Communications
503
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10.1016/j.bbrc.2018.07.128
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Kadri, Hachemi, Lambourne, Olivia A and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2018.
Niclosamide, a drug with many (re)purposes.
ChemMedChem
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10.1002/cmdc.201800100
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Rattan, Hardeep S. and Balzarini, Jan
2018.
The ProTide prodrug technology: from the concept to the clinic.
Journal of Medicinal Chemistry
61
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10.1021/acs.jmedchem.7b00734
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Davey, Martin S., Malde, Roshni, Mykura, Rory C., Baker, Alfie T., Taher, Taher E., Le Duff, Cécile S., Willcox, Benjamin E. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2018.
Synthesis and biological evaluation of (E)-4-hydroxy-3-methylbut2-enyl phosphate (HMBP) aryloxy triester phosphoramidate Prdrugs as activators of Vγ9/Vδ2 T-cells immune response.
Journal of Medicinal Chemistry
61
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10.1021/acs.jmedchem.7b01824
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Barini, Erica, Miccoli, Ageo, Tinarelli, Federico, Mulholand, Katie, Kadri, Hachemi, Khanim, Farhat, Stojanovski, Laste, Read, Kevin D, Burness, Kerry, Blow, Julian J, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513 and Muqit, Miratul
2018.
The anthelmintic drug niclosamide and its analogues activate the Parkinson's Disease associated protein kinase PINK1.
Chembiochem
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10.1002/cbic.201700500
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Salim, Mahboob, Knowles, Timothy J., Baker, Alfie T., Davey, Martin S., Jeeves, Mark, Sridhar, Pooja, Wilkie, John, Willcox, Carrie R., Kadri, Hachemi, Taher, Taher E, Vantourout, Pierre, Hayday, Adrian, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Mohammed, Fiyaz and Willcox, Benjamin E.
2017.
BTN3A1 discriminates γδ T cell phosphoantigens from non-antigenic small molecules via a conformational sensor in its B30.2 domain.
ACS Chemical Biology
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10.1021/acschembio.7b00694
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AlAmri, Mubarak A., Kadri, Hachemi, Dhiani, Binar Asrining, Mahmood, Shumail, Elzwawi, Abdulrahman and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2017.
WNK-signaling inhibitors as potential new antihypertensive drugs.
Chemmedchem
10.1002/cmdc.201700425
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Alamri, Mubarak A., Kadri, Hachemi, Alderwick, Luke J., Simpkins, Nigel S. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2017.
Rafoxanide and Closantel inhibit SPAK and OSR1 kinases by binding to a highly conserved allosteric site on their C-terminal domains.
ChemMedChem
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10.1002/cmdc.201700077
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Osgerby, Laura, Lai, Yu-Chiang, Thornton, Peter J., Amalfitano, Joseph, Le Duff, Cécile S., Jabeen, Iqra, Kadri, Hachemi, Miccoli, Ageo, Tucker, James H. R., Muqit, Miratul M. K. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2017.
Kinetin riboside and its ProTides activate the Parkinson's Disease associated PTEN-Induced Putative Kinase 1 (PINK1) independent of mitochondrial depolarization.
Journal of Medicinal Chemistry
60
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10.1021/acs.jmedchem.6b01897
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Kadri, Hachemi, Alamri, Mubarak A., Navratilova, Iva H., Alderwick, Luke J., Simpkins, Nigel S. and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2017.
Towards the development of small molecule MO25-binders as potential indirect SPAK/OSR1 kinase inhibitors.
ChemBioChem
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10.1002/cbic.201600620
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Kedge, Jonathan L., Nguyen, Huy V., Khan, Zahra, Male, Louise, Hodges, Media K. Ismail Holly V. Roberts Ni, Horswell, Sarah L., Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513 and Tucker, James H. R.
2017.
Organometallic nucleoside analogues: effect of hydroxyalkyl linker length on cancer cell line toxicity.
European Journal of Inorganic Chemistry
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10.1002/ejic.201600853
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Thornton, Peter J., Kadri, Hachemi, Miccoli, Ageo and Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2016.
Nucleoside phosphate and phosphonate prodrug clinical candidates.
Journal of Medicinal Chemistry
59
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10.1021/acs.jmedchem.6b00523
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2016.
The ProTides boom.
Chemmedchem
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10.1002/cmdc.201600156
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Nguyen, Huy V., Sallustrau, Antoine, Balzarini, Jan, Bedford, Matthew R., Eden, John C., Georgousi, Niki, Hodges, Nikolas J., Kedge, Jonathan, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Tselepis, Chris and Tucker, James H. R.
2014.
Organometallic nucleoside analogues with ferrocenyl linker groups: Synthesis and cancer cell line studies.
Journal of Medicinal Chemistry
57
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10.1021/jm500246h
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Ohta, Akihito, Schumacher, Frances-Rose, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Johnson, Clare, Knebel, Axel, Macartney, Thomas J., Wood, Nicola T., Alessi, Dario R. and Kurz, Thimo
2013.
The CUL3–KLHL3 E3 ligase complex mutated in Gordon's hypertension syndrome interacts with and ubiquitylates WNK isoforms: disease-causing mutations in KLHL3 and WNK4 disrupt interaction.
Biochemical Journal
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10.1042/BJ20121903
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Alessi, Dario R., Macartney, Thomas J., Szklarz, Marta, Knapp, Stefan and Elkins, Jonathan M.
2013.
Structural insights into the activation of MST3 by MO25.
Biochemical and Biophysical Research Communications
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10.1016/j.bbrc.2012.12.113
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Chen, Shengxi, Fahmi, Nour Eddine, Nangreave, Ryan C., Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513 and Hecht, Sidney M.
2012.
Synthesis of pdCpAs and transfer RNAs activated with thiothreonine and derivatives.
Bioorganic & Medicinal Chemistry
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10.1016/j.bmc.2012.02.024
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Thastrup, Jacob O., Rafiqi, Fatema H., Vitari, Alberto C., Pozo-Guisado, Eulalia, Deak, Maria, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513 and Alessi, Dario R.
2012.
SPAK/OSR1 regulate NKCC1 and WNK activity: analysis of WNK isoform interactions and activation by T-loop trans-autophosphorylation.
Biochemical Journal
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10.1042/BJ20111879
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Filippi, Beatrice M., de los Heros, Paola, Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Navratilova, Iva, Gourlay, Robert, Deak, Maria, Plater, Lorna, Toth, Rachel, Zeqiraj, Elton and Alessi, Dario R.
2011.
MO25 is a master regulator of SPAK/OSR1 and MST3/MST4/YSK1 protein kinases.
EMBO Journal
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10.1038/emboj.2011.78
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513
2010.
Phosphoramidate Prodrugs Deliver with Potency Against Hepatitis C Virus.
ChemMedChem
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10.1002/cmdc.201000310
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Valente, Rocco, Mottram, Huw James, Walsby, Elisabeth Jane ORCID: https://orcid.org/0000-0001-8523-5017, Mills, Kenneth Ian, Balzarini, Jan and McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X
2010.
Phosphoramidates of 2′-β-d-arabinouridine (AraU) as phosphate prodrugs; design, synthesis, in vitro activity and metabolism.
Bioorganic & Medicinal Chemistry
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10.1016/j.bmc.2010.02.059
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Balzarini, Jan and McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X
2010.
The design, synthesis and antiviral evaluation of a series of 5-trimethylsilyl-1-β-D-(arabinofuranosyl)uracil phosphoramidate ProTides.
Antiviral Chemistry & Chemotherapy
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10.3851/IMP1476
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513 and De Clercq, Erik
2010.
Twenty-Six Years of Anti-HIV Drug Discovery: Where Do We Stand and Where Do We Go?
Journal of Medicinal Chemistry
53
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10.1021/jm900492g
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Balzarini, J. and McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X
2009.
Aryloxy Phosphoramidate Triesters: a Technology for Delivering Monophosphorylated Nucleosides and Sugars into Cells.
Chemmedchem
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10.1002/cmdc.200900289
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, Balzarini, J. and McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X
2009.
An investigation into the anti-HIV activity of 2 ',3 '-didehydro-2 ',3 '-dideoxyuridine (d4U) and 2 ',3 '-dideoxyuridine (ddU) phosphoramidate 'ProTide' derivatives.
Organic and Biomolecular Chemistry
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10.1039/b904276h
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X, Brancale, Andrea ORCID: https://orcid.org/0000-0002-9728-3419 and Balzarini, J.
2007.
Design, synthesis, and anti-HIV activity of 2',3'-didehydro-2',3'-dideoxyuridine (d4U), 2',3'-dideoxyuridine (ddU) phosphoramidate "ProTide' derivatives.
Biorganic and Medicinal Chemistry Letters
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10.1016/j.bmcl.2007.04.043
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Mehellou, Youcef ORCID: https://orcid.org/0000-0001-5720-8513, McGuigan, Christopher ORCID: https://orcid.org/0000-0001-8409-710X and Balzarini, J.
2007.
The design, synthesis and Anti-HIV activity of a selected group of 2 ',3 '-didehydro-2 ',3 '-dideoxyguanosine (d4G) and 2 ',3 '-dideoxyguanosine (ddG) 'ProTide' derivatives.
Antiviral Research
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