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1.
J Med Chem ; 64(19): 14332-14343, 2021 10 14.
Artículo en Inglés | MEDLINE | ID: mdl-34524803

RESUMEN

In addition to a variety of viral-glycoprotein receptors (e.g., heparan sulfate, Niemann-Pick C1, etc.), dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN), from the C-type lectin receptor family, plays one of the most important pathogenic functions for a wide range of viruses (e.g., Ebola, human cytomegalovirus (HCMV), HIV-1, severe acute respiratory syndrome coronavirus 2, etc.) that invade host cells before replication; thus, its inhibition represents a relevant extracellular antiviral therapy. We report two novel p-tBu-calixarene glycoclusters 1 and 2, bearing tetrahydroxamic acid groups, which exhibit micromolar inhibition of soluble DC-SIGN binding and provide nanomolar IC50 inhibition of both DC-SIGN-dependent Jurkat cis-cell infection by viral particle pseudotyped with Ebola virus glycoprotein and the HCMV-gB-recombinant glycoprotein interaction with monocyte-derived dendritic cells expressing DC-SIGN. A unique cooperative involvement of sugar, linker, and calixarene core is likely behind the strong avidity of DC-SIGN for these low-valent systems. We claim herein new promising candidates for the rational development of a large spectrum of antiviral therapeutics.


Asunto(s)
Calixarenos/química , Moléculas de Adhesión Celular/antagonistas & inhibidores , Glicoconjugados/metabolismo , Glicoproteínas/antagonistas & inhibidores , Ácidos Hidroxámicos/química , Lectinas Tipo C/antagonistas & inhibidores , Fenoles/química , Receptores de Superficie Celular/antagonistas & inhibidores , Proteínas Virales/antagonistas & inhibidores , Antivirales/química , Antivirales/metabolismo , Antivirales/farmacología , Moléculas de Adhesión Celular/metabolismo , Línea Celular , Citomegalovirus/metabolismo , Células Dendríticas/citología , Células Dendríticas/metabolismo , Ebolavirus/fisiología , Glicoconjugados/química , Glicoconjugados/farmacología , Glicoproteínas/genética , Glicoproteínas/metabolismo , Humanos , Células Jurkat , Lectinas Tipo C/metabolismo , Modelos Biológicos , Unión Proteica , Receptores de Superficie Celular/metabolismo , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/química , Proteínas Recombinantes/aislamiento & purificación , Proteínas Virales/genética , Proteínas Virales/metabolismo
2.
J Med Chem ; 62(17): 7722-7738, 2019 09 12.
Artículo en Inglés | MEDLINE | ID: mdl-31449405

RESUMEN

Opportunistic Gram-negative Pseudomonas aeruginosa uses adhesins (e.g., LecA and LecB lectins, type VI pili and flagella) and iron to invade host cells with the formation of a biofilm, a thick barrier that protects bacteria from drugs and host immune system. Hindering iron uptake and disrupting adhesins' function could be a relevant antipseudomonal strategy. To test this hypothesis, we designed an iron-chelating glycocluster incorporating a tetrahydroxamic acid and α-l-fucose bearing linker to interfere with both iron uptake and the glycan recognition process involving the LecB lectin. Iron depletion led to increased production of the siderophore pyoverdine by P. aeruginosa to counteract the loss of iron uptake, and strong biofilm inhibition was observed not only with the α-l-fucocluster (72%), but also with its α-d-manno (84%), and α-d-gluco (92%) counterparts used as negative controls. This unprecedented finding suggests that both LecB and biofilm inhibition are closely related to the presence of hydroxamic acid groups.


Asunto(s)
Antibacterianos/farmacología , Biopelículas/efectos de los fármacos , Glicoconjugados/farmacología , Ácidos Hidroxámicos/farmacología , Pseudomonas aeruginosa/efectos de los fármacos , Adhesinas Bacterianas/efectos de los fármacos , Antibacterianos/síntesis química , Antibacterianos/química , Relación Dosis-Respuesta a Droga , Glicoconjugados/síntesis química , Glicoconjugados/química , Ácidos Hidroxámicos/síntesis química , Ácidos Hidroxámicos/química , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Relación Estructura-Actividad
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