Synthesis and Antiproliferative Evaluation of d-Glucuronamide-Based Nucleosides and (Triazolyl)methyl Amide-Linked Pseudodisaccharide Nucleosides
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
CEECIND/03881/2018
'Fundacão para a Ciência e Tecnologia' (FCT)
EXPL/MED-QUI/1017/2021
'Fundacão para a Ciência e Tecnologia' (FCT)
UIDB/00100/2020
'Fundacão para a Ciência e Tecnologia' (FCT)
UIDP/00100/2020
'Fundacão para a Ciência e Tecnologia' (FCT)
LA/P/0056/2020
'Fundacão para a Ciência e Tecnologia' (FCT)
Instituto Nacional de Gestão de Bolsas de Estudos do Governo de Angola
Instituto Superior de Ciências de Educação da Huíla
EXPL/MED-QUI/1017/2021 (https://doi.org/10.54499/EXPL/MED-QUI/1017/2021)
'Fundacão para a Ciência e Tecnologia' (FCT)
- Keywords
- N-glycosylation, antiproliferative activity, cycloaddition, d-glucuronamide, nucleoside analogs,
- MeSH
- Amides * pharmacology MeSH
- Glucuronates MeSH
- Humans MeSH
- Nucleosides * pharmacology MeSH
- Purine Nucleosides MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amides * MeSH
- glucuronamide MeSH Browser
- Glucuronates MeSH
- Nucleosides * MeSH
- Purine Nucleosides MeSH
The synthesis and antiproliferative evaluation of novel d-glucopyranuronamide-containing nucleosides is described. Based on our previously reported anticancer d-glucuronamide-based nucleosides, new analogues comprising N/O-dodecyl or N-propargyl substituents at the glucuronamide unit and anomerically-N-linked 2-acetamido-6-chloropurine, 6-chloropurine or 4-(6-chloropurinyl)methyl triazole motifs were synthesized in 4-6 steps starting from acetonide-protected glucofuranurono-6,3-lactone. The methodologies were based on the access to N-substituted glycopyranuronamide precursors, namely 1,2-O-acetyl derivatives or glucuronoamidyl azides for further nucleobase N-glycosylation or 1,3-dipolar cycloaddition with N9 - and N7 -propargyl-6-chloropurines, respectively. N-Propargyl glucuronamide-based N9 -purine nucleosides were converted into (triazolyl)methyl amide-6,6-linked pseudodisaccharide nucleosides via cycloaddition with methyl 6-azido-glucopyranoside. A CuI/Amberlyst A-21 catalytic system employed in the cycloaddition reactions also effected conversion into 6-dimethylaminopurine nucleosides. Antiproliferative evaluation in chronic myeloid leukemia (K562) and breast cancer (MCF-7) cells revealed significant effects exhibited by the synthesized monododecylated purine-containing nucleosides. A N-propargyl 3-O-dodecyl glucuronamide derivative comprising a N9 -β-linked 6-chloropurine moiety was the most active compound against MCF-7 cells (GI50 =11.9 μM) while a related α-(purinyl)methyltriazole nucleoside comprising a N7 -linked 6-chloropurine moiety exhibited the highest activity against K562 cells (GI50 =8.0 μM). Flow cytometry and immunoblotting analysis of apoptosis-related proteins in K562 cells treated with the N-propargyl 3-O-dodecyl glucuronamide-based N9 -linked 6-chloropurine nucleoside indicated that it acts via apoptosis induction.
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