keyword
https://read.qxmd.com/read/38521735/time-to-diagnosis-and-its-predictors-in-syndromes-associated-with-frontotemporal-lobar-degeneration
#1
JOURNAL ARTICLE
Ilenia Libri, Daniele Altomare, Valeria Bracca, Jasmine Rivolta, Valentina Cantoni, Irene Mattioli, Antonella Alberici, Barbara Borroni
OBJECTIVES: Frontotemporal Lobar Degeneration (FTLD) causes a heterogeneous group of neurodegenerative disorders with a wide range of clinical features. This might delay time to diagnosis. The aim of the present study is to establish time to diagnosis and its predictors in patients with FTLD-associated syndromes. DESIGN: Retrospective study. SETTING: Tertiary referral center. PARTICIPANTS: A total of 1029 patients with FTLD-associated syndromes (age: 68 [61-73] years, females: 46%) from 1999 to 2023 were included in the present study...
March 7, 2024: American Journal of Geriatric Psychiatry
https://read.qxmd.com/read/35479228/first-total-synthesis-of-chromanone-a-preparation-of-related-compounds-and-evaluation-of-their-antifungal-activity-against-candida-albicans-a-biofilm-forming-agent
#2
JOURNAL ARTICLE
Iván Cortés, Estefanía Cordisco, Teodoro S Kaufman, Maximiliano A Sortino, Laura A Svetaz, Andrea B J Bracca
A straightforward and convenient approach for the first total syntheses of chromanone A and a related 7-OMe substituted natural product is reported. These unique C-3 substituted 2-hydroxymethyl chromones were recently isolated as fungal metabolites. Chromanone A was synthesized in 25.3% overall yield from the readily available pyrocatechol, whereas the second natural product was prepared in 39.7% global yield. A small library of chromones, including both natural products and some of their synthetic heterocyclic precursors, was evaluated against Candida albicans ATCC 10231, a biofilm forming agent...
May 27, 2021: RSC Advances
https://read.qxmd.com/read/15878275/synthesis-of-tricyclic-analogs-of-stephaoxocanidine-and-their-evaluation-as-acetylcholinesterase-inhibitors
#3
JOURNAL ARTICLE
Darío A Bianchi, Guillermo Schmeda Hirschmann, Cristina Theoduloz, Andrea B J Bracca, Teodoro S Kaufman
The synthesis of simplified analogs of the novel isoquinoline alkaloid stephaoxocanidine, carrying the oxazaphenalene ABC-ring system of the natural product, and their activity as inhibitors of the enzyme acetylcholinesterase, are reported. 5,6-Dimethoxy-7H -8-oxa-1-aza-phenalen-9-one (5) was as active as a Narcissus extract enriched in galantamine.
June 2, 2005: Bioorganic & Medicinal Chemistry Letters
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