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1.
J Acoust Soc Am ; 146(5): 3652, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31795652

RESUMEN

Currently, no approved medicines are available for the prevention or treatment of hearing loss. Pharmaceutical industry productivity across all therapeutic indications has historically been disappointing, with a 90% chance of failure in delivering a marketed drug after entering clinical evaluation. To address these failings, initiatives have been applied in the three cornerstones of medicine discovery: target selection, clinical candidate selection, and clinical studies. These changes aimed to enable data-informed decisions on the translation of preclinical observations into a safe, clinically effective medicine by ensuring the best biological target is selected, the most appropriate chemical entity is advanced, and that the clinical studies enroll the correct patients. The specific underlying pathologies need to be known to allow appropriate patient selection, so improved diagnostics are required, as are methodologies for measuring in the inner ear target engagement, drug delivery and pharmacokinetics. The different therapeutic strategies of protecting hearing or preventing hearing loss versus restoring hearing are reviewed along with potential treatments for tinnitus. Examples of current investigational drugs are discussed to highlight key challenges in drug discovery and the learnings being applied to improve the probability of success of launching a marketed medicine.


Asunto(s)
Descubrimiento de Drogas/métodos , Industria Farmacéutica/métodos , Pérdida Auditiva/tratamiento farmacológico , Animales , Ensayos Clínicos como Asunto , Industria Farmacéutica/economía , Humanos , Fármacos Neuroprotectores/uso terapéutico , Investigación Biomédica Traslacional/métodos
4.
Org Lett ; 5(7): 999-1002, 2003 Apr 03.
Artículo en Inglés | MEDLINE | ID: mdl-12659558

RESUMEN

[reaction: see text] The partial reduction of electron-deficient 2,5-disubstituted pyrroles has been developed into a flexible procedure that gives control of relative stereochemistry by variation of the reduction conditions. After the reaction, the pyrroline products were dihydroxylated at C-3,4 to give either the cis or trans isomers; this flexibility means that a variety of polyhydroxylated pyrrolidines can be prepared in a short sequence. Finally, this method was applied to a synthesis of the naturally occurring glycosidase inhibitor DMDP.


Asunto(s)
Alcaloides/síntesis química , Pirroles/química , Pirrolidinas , Alcaloides/química , Inhibidores Enzimáticos/síntesis química , Inhibidores Enzimáticos/química , Glicósido Hidrolasas/antagonistas & inhibidores , Iminofuranosas , Isomerismo , Manitol/análogos & derivados , Estructura Molecular
5.
Org Lett ; 6(18): 3055-8, 2004 Sep 02.
Artículo en Inglés | MEDLINE | ID: mdl-15330586

RESUMEN

[reaction: see text] The partial reduction of 2,5-pyrrole diester 1 followed by enantioselective protonation in situ to furnish synthetically useful building blocks is described. An enantiomeric excess of up to 74% was achieved using (-)-ephedrine and related analogues as chiral proton sources. The pyrroline product obtained could be recrystallized to give enantiomerically pure material.


Asunto(s)
Técnicas Químicas Combinatorias , Efedrina/química , Pirroles/química , Catálisis , Indicadores y Reactivos , Estructura Molecular , Oxidación-Reducción , Pirroles/análisis , Pirroles/síntesis química , Estereoisomerismo
6.
Chem Commun (Camb) ; (12): 1422-3, 2004 Jun 21.
Artículo en Inglés | MEDLINE | ID: mdl-15179495

RESUMEN

Access to the synthetically important tetrahydropyridine motif has been achieved by radical rearrangement of pyrrolines obtained from the Birch reduction of electron-deficient pyrroles.

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