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1.
Chimia (Aarau) ; 75(6): 508-513, 2021 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-34233814

RESUMEN

Polyphor's macrocycle platform led to the discovery of novel antibiotics addressing specifically Gramnegative bacteria by targeting outer membrane proteins. Furthermore, POL6014, an inhibitor of neutrophile elastase and balixafortide, a CXCR4 inhibitor have been discovered and developed from the platform. Currently a combination of balixafortide and eribulin is in Phase III clinical trial for the treatment of patients with advanced metastatic HER2-negative breast cancer.


Asunto(s)
Neoplasias de la Mama , Cetonas , Femenino , Humanos
2.
Med Drug Discov ; 9: 100078, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33398258

RESUMEN

This review covers some of the recent progress in the field of peptide antibiotics with a focus on compounds with novel or established mode of action and with demonstrated efficacy in animal infection models. Novel drug discovery approaches, linear and macrocyclic peptide antibiotics, lipopeptides like the polymyxins as well as peptides addressing targets located in the plasma membrane or in the outer membrane of bacterial cells are discussed.

3.
Methods Mol Biol ; 2001: 147-202, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31134572

RESUMEN

This review describes a selection of macrocyclic natural products and structurally modified analogs containing peptidic and non-peptidic elements as structural features that potentially modulate cellular permeability. Examples range from exclusively peptidic structures like cyclosporin A or phepropeptins to compounds with mostly non-peptidic character, such as telomestatin or largazole. Furthermore, semisynthetic approaches and synthesis platforms to generate general and focused libraries of compounds at the interface of cyclic peptides and non-peptidic macrocycles are discussed.


Asunto(s)
Compuestos Macrocíclicos/química , Péptidos Cíclicos/química , Productos Biológicos , Ciclización , Depsipéptidos/química , Depsipéptidos/metabolismo , Humanos , Lactonas/química , Lactonas/metabolismo , Compuestos Macrocíclicos/síntesis química , Oxazoles/química , Oxazoles/metabolismo , Biblioteca de Péptidos , Péptidos Cíclicos/síntesis química , Péptidos Cíclicos/metabolismo , Permeabilidad , Conformación Proteica , Compuestos de Espiro/química , Compuestos de Espiro/metabolismo , Estreptograminas/química , Estreptograminas/metabolismo , Tiazoles/química , Tiazoles/metabolismo
4.
Chimia (Aarau) ; 71(10): 678-702, 2017 Oct 25.
Artículo en Inglés | MEDLINE | ID: mdl-29070413

RESUMEN

Macrocyclic compounds have recently received increasing attention in drug discovery as these compounds offer the potential to modulate difficult targets and to access novel chemotypes. Approaches towards libraries of macrocyclic compounds based on modular organic synthesis and applications of these technology platforms to find and improve biologically active compounds are introduced in this minireview. Alternatively, lead compounds may be obtained by truncation and modification of macrocyclic natural products. Selected medicinal chemistry programs are discussed, illustrating a macrocyclization approach toward ligands with improved properties. The design of such ligands is often informed by X-ray crystal structures of protein-ligand complexes. Efforts to understand cellular permeability and oral bioavailability of cyclic peptides and non-peptidic macrocycles are summarized.


Asunto(s)
Química Farmacéutica , Diseño de Fármacos , Compuestos Macrocíclicos/síntesis química , Ciclización , Compuestos Macrocíclicos/química , Péptidos Cíclicos/síntesis química
5.
J Med Chem ; 46(7): 1153-64, 2003 Mar 27.
Artículo en Inglés | MEDLINE | ID: mdl-12646026

RESUMEN

Data from both our own and literature studies of the biochemistry and inhibition of influenza virus endonuclease was combined with data on the mechanism of action and the likely active site mechanism to propose a pharmacophore. The pharmacophore was used to design a novel structural class of inhibitors, some of which were found to have activities similar to that of known influenza endonuclease inhibitors and were also antiviral in cell culture.


Asunto(s)
Antivirales/síntesis química , Endonucleasas/antagonistas & inhibidores , Inhibidores Enzimáticos/síntesis química , Animales , Antivirales/química , Antivirales/farmacología , Sitios de Unión , Butiratos/síntesis química , Butiratos/química , Butiratos/farmacología , Línea Celular , Técnicas Químicas Combinatorias , ARN Polimerasas Dirigidas por ADN/química , Bases de Datos Factuales , Perros , Endonucleasas/química , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Compuestos Heterocíclicos con 3 Anillos/síntesis química , Compuestos Heterocíclicos con 3 Anillos/química , Compuestos Heterocíclicos con 3 Anillos/farmacología , Compuestos Heterocíclicos de 4 o más Anillos/síntesis química , Compuestos Heterocíclicos de 4 o más Anillos/química , Compuestos Heterocíclicos de 4 o más Anillos/farmacología , Virus de la Influenza A/efectos de los fármacos , Virus de la Influenza A/enzimología , Virus de la Influenza B/efectos de los fármacos , Virus de la Influenza B/enzimología , Cetoácidos/síntesis química , Cetoácidos/química , Cetoácidos/farmacología , Modelos Moleculares , Ftalimidas/síntesis química , Ftalimidas/química , Ftalimidas/farmacología , Unión Proteica , Relación Estructura-Actividad
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