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[This corrects the article DOI: 10.1021/acs.oprd.1c00368.].
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An efficient synthesis of α-amino-γ-lactone ketolide (3) was developed, which provided a versatile intermediate for the incorporation of a variety of aryl and heteroaryl groups onto the C-21 position of clarithromycin via HBTU-mediated amidation. The biological data for this important new class of macrolides revealed significantly potent activity against erythromycin-susceptible strains as well as efflux-resistant and erythromycin MLSB-resistant strains of S. pneumoniae and S. pyogenes. In addition, ketolide 11o showed excellent in vitro antibacterial activity against H. influenzae strain as compared to telithromycin. These results indicate that C-21 substituted γ-lactone ketolides have potential as a next generation macrolide antibiotics.
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The identification of structurally novel analogues of ketamine and phencyclidine (PCP), as NMDA receptor antagonists, with low to moderate potency at GluN2A and GluN2B receptors is discussed. In particular, some examples, such as compounds 6 and 10, shows decreased calculated lipophilicity, when compared to PCP, while retaining moderate activity. Moreover, the germinal aryl amino substituted lactam ring, as exemplified in compounds 7-10 and 11-13, constitutes a novel scaffold with potential application in the design of biologically active compounds.
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Ketamina/farmacología , Fenciclidina/farmacología , Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores , Ketamina/análogos & derivados , Fenciclidina/análogos & derivadosRESUMEN
A new class of selective NPS antagonist was developed starting from a commercially available product identified by screening activities. Experimental NMR observations and computational experiments allowed the discovery of a new class of derivatives. 5-Phenyl-2-[2-(1-piperidinylcarbonyl)phenyl]-2,3-dihydro-1H-pyrrolo[1,2-c]imidazol-1-one represents a new lead compound in the NPS antagonist field.
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Compuestos de Azabiciclo/química , Imidazoles/química , Neuropéptidos/antagonistas & inhibidores , Piperidinas/química , Animales , Simulación por Computador , Diseño de Fármacos , Humanos , Imidazoles/síntesis química , Imidazoles/farmacología , Microsomas Hepáticos/metabolismo , Neuropéptidos/metabolismo , Ratas , TermodinámicaRESUMEN
The synthesis and the structure activity of a new series of pyrrolo[1,2-a]pyrazine is reported. These molecules are potent and selective non-competitive mGluR5 antagonists and may shed new light on the pattern of substitution tolerated by this receptor.
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Pirazinas/farmacología , Pirroles/farmacología , Receptores de Glutamato Metabotrópico/antagonistas & inhibidores , Proteínas de Transporte de Dopamina a través de la Membrana Plasmática/antagonistas & inhibidores , Fluorescencia , Humanos , Estructura Molecular , Proteínas de Transporte de Noradrenalina a través de la Membrana Plasmática/antagonistas & inhibidores , Pirazinas/síntesis química , Pirroles/síntesis química , Receptor del Glutamato Metabotropico 5 , Relación Estructura-ActividadRESUMEN
One of the still unresolved problems in parallel synthesis is the availability of a general and rapid method for the transformation of a primary amine into the corresponding secondary amine without the issue of polyalkylation. Following the Fukuyama method, which is based on the alkylation of o-nitrobenzenesulfonamides, followed by removal of the sulfonyl group, we have developed a simple protocol which can be easily applied to parallel synthesis making use of supported reagents and scavengers. To verify the robustness of the method, a small representative array of secondary amines have been prepared. Moreover, taking advantage of the possibility to use different supported reagents in the same pot, we also prepared, starting from primary amines, a series of differently substituted tertiary amines.
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Aminas/síntesis química , Alquilación , Aminas/química , Metilación , Estructura Molecular , EstereoisomerismoRESUMEN
Different arene Cr(CO)(3) complexes were supported on a polystyrene isonitrile resin by photochemical-promoted replacement of a chromium carbonyl ligand by the NC group. The supported complexes proved to be stable and were successfully used for further transformations. In particular, the reactivity of dichlorobenzene complexes to different nucleophiles was investigated and found to be comparable with that of the parent Cr(CO)(3) complexes.
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Compuestos de Cromo/síntesis química , Polímeros/síntesis química , Tecnología Farmacéutica/métodos , Compuestos de Cromo/química , Polímeros/químicaRESUMEN
Metabotropic glutamate receptors (mGluRs) are an unusual family of G-protein coupled receptor (GPCR), and are characterised by a large extracellular N-terminal domain that contains the glutamate binding site. We have identified a new class of non-competitive metabotropic glutamate receptor 1 (mGluR1) antagonists, 2,4-dicarboxy-pyrroles which are endowed with nanomolar potency. They interact within the 7 transmembrane (7TM) domain of the receptor and show antinociceptive properties when tested in a number of different animal models.