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Novel diarylamides and diarylureas with N-substitution dependent activity against medulloblastoma

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Autore
Lawson C., Ahmed Alta T.B., Moschou G., Skamnaki V., Solovou T.G.A., Topham C., Hayes J., Snape T.J.
Data
2021
Language
en
DOI
10.1016/j.ejmech.2021.113751
Soggetto
amide
antineoplastic agent
urea
cell proliferation
cerebellum tumor
chemical structure
chemistry
dose response
drug effect
drug screening
human
medulloblastoma
pathology
structure activity relation
synthesis
tumor cell line
Amides
Antineoplastic Agents
Cell Line, Tumor
Cell Proliferation
Cerebellar Neoplasms
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
Humans
Medulloblastoma
Molecular Structure
Structure-Activity Relationship
Urea
Elsevier Masson s.r.l.
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Abstract
Medulloblastoma – highly aggressive and heterogeneous tumours of the cerebellum – account for 15–20% of all childhood brain tumours, and are the most common high-grade childhood embryonal tumour of the central nervous system. Herein, potent in vitro anticancer activity against two established medulloblastoma cell lines of the sonic hedgehog subgroup, namely DAOY (p53 mutant) and ONS-76 (p53 wild type), has been achieved. A number of first-generation diarylamides and diarylureas were evaluated and activity is likely to be, in-part, conformation-dependent. The most active compound from this first-generation set of compounds, 1-naphthyl derivative 4b, was selected and a second-generation of compounds were optimised and tested for activity against the medulloblastoma cell lines. This process resulted in drug-like compounds with up to sixty times the activity (sub-micromolar) of the first-generation – thus providing potent new leads for further study. © 2021
URI
http://hdl.handle.net/11615/75721
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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