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Anders Eneroth

Observed names: A Eneroth, A. Eneroth
Institution: Uppsala University
OpenAlex ID: A5075013844
Evaluation of a vincristine resistant Caco-2 cell line for use in a calcein AM extrusion screening assay for P-glycoprotein interaction
2001 · A Eneroth, E Åström, et al. · European Journal of Pharmaceutical Sciences · 113
Imitation of β-lactam binding enables broad-spectrum metallo-β-lactamase inhibitors
2021 · Jürgen Brem, Tharindi Panduwawala, et al. · Nature Chemistry · 98
Synthesis and SAR of potent inhibitors of the Hepatitis C virus NS3/4A protease: Exploration of P2 quinazoline substituents
2010 · Magnus Nilsson, Anna Karin Belfrage, et al. · Bioorganic & Medicinal Chemistry Letters · 25
Discovery of novel, potent and bioavailable proline-urea based macrocyclic HCV NS3/4A protease inhibitors
2008 · Sandrine Vendeville, Magnus Nilsson, et al. · Bioorganic & Medicinal Chemistry Letters · 24
Interferon-?-like immunoreactivity in developing rat spinal ganglia neuronsin vivo andin vitro
1991 · A. Eneroth, K. Kristensson, et al. · Journal of Neurocytology · 21
Discovery of β-d-2′-deoxy-2′-dichlorouridine nucleotide prodrugs as potent inhibitors of hepatitis C virus replication
2017 · Pedro Pinho, Genadiy Kalayanov, et al. · Bioorganic & Medicinal Chemistry Letters · 20
Preclinical Evaluation of 1H-Benzylindole Derivatives as Novel Human Immunodeficiency Virus Integrase Strand Transfer Inhibitors
2008 · Anneleen Hombrouck, Barbara Van Remoortel, et al. · Antimicrobial Agents and Chemotherapy · 19
Design and synthesis of potent macrocyclic renin inhibitors
2010 · Christian Sund, Oscar Belda, et al. · Bioorganic & Medicinal Chemistry Letters · 17
Bidirectional signals betweenTrypanosoma brucei brucei and dorsal root ganglion neurons
1992 · A. Eneroth, M. Bakhiet, et al. · Journal of Neurocytology · 13
Interferon‐γ‐Like immunoreactivity in sensory neurons may influence the replication of sendai and mumps viruses
1992 · A. Eneroth, T. Andersson, et al. · Journal of Neuroscience Research · 13
Design and synthesis of potent hydroxyethylamine (HEA) BACE-1 inhibitors carrying prime side 4,5,6,7-tetrahydrobenzazole and 4,5,6,7-tetrahydropyridinoazole templates
2012 · Christian Sund, Oscar Belda, et al. · Bioorganic & Medicinal Chemistry Letters · 12
The novel L-nucleoside analogue, 5-Fluorotroxacitabine, displays potent efficacy against acute myeloid leukemia
2019 · Aniket Bankar, Thirushi Piyumika Siriwardena, et al. · Haematologica · 5
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MIV-802, a uridine nucleotide prodrug, is a more potent inhibitor of hepatitis C virus genotype 3 replication than sofosbuvir
2017 · E. Lana, E. Brenndörfer, et al. · Journal of Hepatology · 2
P0688 : Preclinical characterisation of MIV-802, a novel uridine nucleotide HCV NS5B polymerase inhibitor, for treatment of hepatitis C virus infection
2015 · A. Lindqvist, H. Kylefjord, et al. · Journal of Hepatology · 2
A new approach for the pathogenesis of human African trypanosomiasis.
1994 · K Kristensson, A Eneroth, et al. · PubMed · 2
5-Fluorotroxacitabine Displays Potent Anti-Leukemic Effects and Circumvents Resistance to Ara-C
2018 · Aniket Bankar, Thirushi Piyumika Siriwardena, et al. · Blood · 1
Liver-targeting with the novel nucleotide prodrug MIV-818 designed for the treatment of liver cancers
2017 · R. Bethell, K. Tunblad, et al. · Journal of Hepatology · 1
Protides of 5-Fluorotroxacitabine Display Potent Anti-Proliferative Properties and Circumvent Deoxycytidine Kinase-Mediated Resistance Associated with Cytotoxic Cytidine Analogues; A Novel Approach for Acute Myeloid Leukemia
2018 · Pedro Pinho, Helen Kylefjord, et al. · Blood
Abstract 5101: Defining exposure-PD and efficacy relationships with the novel liver-targeting nucleotide prodrug MIV-818 for the treatment of liver cancers
2017 · Mark Albertella, Biljana Rizoska, et al. · Cancer Research
Interactions between Trypanosoma brucei brucei and dorsal root ganglia neurons
1994 · M. Bakhiet, A. Eneroth, et al. · Journal of Neuroimmunology
Works count: 20
Citation count: 388
H-index: 11
I10-index: 11
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