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Profil bibliographique

Marwa Nadia Rahimi

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

17Publications signalées
299Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Neuropeptides and Animal PhysiologyChemical Synthesis and AnalysisClick Chemistry and ApplicationsComputational Drug Discovery MethodsNeuroendocrine Tumor Research Advances

Les publications récentes

Accès ouvert 2026 erratum OpenAlex

Correction: Evaluating the therapeutic efficacy of gastramide theranostics targeting cholecystokinin-2 receptors in a preclinical setting

Marwa Nadia Rahimi, Jo‐Anne Pinson, J.P. Hilton-Proctor, Jessica Van Zuylekom et autres

Correction for ‘Evaluating the therapeutic efficacy of gastramide theranostics targeting cholecystokinin-2 receptors in a preclinical setting’ by Marwa N. Rahimi et al. , RSC Adv. , 2026, 16 , 2123–2132, https://doi.org/10.1039/D5RA08789A.

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0 citations RSC Advances
Accès ouvert 2024 article OpenAlex

Precision peptide theranostics: developing N- to C-terminus optimized theranostics targeting cholecystokinin-2 receptor

Marwa Nadia Rahimi, Alicia Corlett, Jessica Van Zuylekom, Marc‐Antoine Sani et autres

Peptides are ideal for theranostic development as they afford rapid target accumulation, fast clearance from background tissue, and exhibit good tissue penetration.Previously, we developed a novel series of peptides that presented discreet folding propensity leading to an optimal candidate [ 68 Ga]Ga-DOTA-GA1 …

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7 citations Theranostics
2023 article OpenAlex

Development of Highly Potent Clinical Candidates for Theranostic Applications against Cholecystokinin-2 Receptor Positive Cancers

Alicia Corlett, Jo‐Anne Pinson, Marwa Nadia Rahimi, Jessica Van Zuylekom et autres

Peptide receptor radionuclide therapy (PRRT) is a promising form of systemic radiation therapy designed to eradicate cancer. Cholecystokinin-2 receptor (CCK 2 R) is an important molecular target that is highly expressed in a range of cancers. This study describes the synthesis and …

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9 citations Journal of Medicinal Chemistry
Accès ouvert 2021 paratext OpenAlex

Frontispiece: Cyclic Peptides as Drugs for Intracellular Targets: The Next Frontier in Peptide Therapeutic Development

Laura K. Buckton, Marwa Nadia Rahimi, Shelli R. McAlpine

In their review article on page 1487, S. R. McAlpine et al., describe recent strategies used to develop cell permeable cyclic peptides that retain binding to their biological target once inside the cell. They discuss chemical strategies that have produced molecules with …

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1 citation Chemistry - A European Journal
2020 article OpenAlex

Cyclic Peptides as Drugs for Intracellular Targets: The Next Frontier in Peptide Therapeutic Development

Laura K. Buckton, Marwa Nadia Rahimi, Shelli R. McAlpine

Developing macrocyclic peptides that can reach intracellular targets is a significant challenge. This review discusses the most recent strategies used to develop cell permeable cyclic peptides that maintain binding to their biological target inside the cell. Macrocyclic peptides are unique from small …

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201 citations Chemistry - A European Journal
Accès ouvert 2019 article OpenAlex

Delivering bioactive cyclic peptides that target Hsp90 as prodrugs

Yuantao Huo, Laura K. Buckton, Jack L. Bennett, Eloise C. Smith et autres

The most challenging issue facing peptide drug development is producing a molecule with optimal physical properties while maintaining target binding affinity. Masking peptides with protecting groups that can be removed inside the cell, produces a cell-permeable peptide, which theoretically can maintain its …

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3 citations Journal of Enzyme Inhibition and Medicinal Chemistry

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