Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
1.
Internist (Berl) ; 56(1): 80-3, 2015 Jan.
Artículo en Alemán | MEDLINE | ID: mdl-25583311

RESUMEN

A 54-year-old man presented with a 6-week history of chronic diarrhea and weight loss of 11 kg after returning from a holiday in Thailand. The patient had a 9-year history of an untreated HIV infection. Despite treatment of a culture-proven Shigella enteritis and strongyloidiasis the symptoms persisted. Finally, cytomegalovirus (CMV) colitis was diagnosed by colonoscopy. The patient recovered completely after starting antiretroviral and valganciclovir treatment. An additional opportunistic infection with multiresistant pulmonary tuberculosis was diagnosed.


Asunto(s)
Infecciones por Citomegalovirus/complicaciones , Infecciones por Citomegalovirus/tratamiento farmacológico , Diarrea/etiología , Infecciones por VIH/complicaciones , Infecciones por VIH/tratamiento farmacológico , Delgadez/etiología , Antirretrovirales/administración & dosificación , Enfermedad Crónica , Colitis , Infecciones por Citomegalovirus/diagnóstico , Diarrea/diagnóstico , Diarrea/prevención & control , Ganciclovir/administración & dosificación , Ganciclovir/análogos & derivados , Infecciones por VIH/inducido químicamente , Humanos , Masculino , Persona de Mediana Edad , Delgadez/diagnóstico , Delgadez/prevención & control , Resultado del Tratamiento , Valganciclovir , Pérdida de Peso
2.
Biopolymers ; 100(2): 154-9, 2013 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-23616099

RESUMEN

A series of compounds containing either non-proteinogenic ß-/γ-amino acids or N-substituted ß-alanine residues (ß-peptoid units) in P1 specificity position were synthesized based on the structure of sunflower trypsin inhibitor 1 (SFTI-1). The compounds were synthesized on a solid support; the N-substituted ß-alanines (ßNhlys and ßNhphe) were introduced into a peptidomimetic chain via a two-step approach using acryloyl chloride and an appropriate primary amine. The inhibitory activities were characterized in vitro against bovine α-chymotrypsin or bovine ß-trypsin. Three analogues displayed activity comparable to fully proteinogenic counterparts-monocyclic SFTI-1 and [Phe(5)]SFTI-1. Moreover, all active peptidomimetics were resistant toward proteolytic degradation, even after 24-h incubation at room temperature.


Asunto(s)
Aminoácidos , beta-Alanina , Aminoácidos/química , Animales , Peptoides , Tripsina/química , Inhibidores de Tripsina/química
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA