Chemical biology, molecular mechanism and clinical perspective of γ-secretase modulators in Alzheimer's disease
B Bulic, J Ness, S Hahn, A Rennhack… - Current …, 2011 - ingentaconnect.com
Comprehensive evidence supports that oligomerization and accumulation of amyloidogenic
Aβ42 peptides in brain is crucial in the pathogenesis of both familial and sporadic forms of …
Aβ42 peptides in brain is crucial in the pathogenesis of both familial and sporadic forms of …
Cognitive enhancers (nootropics). Part 2: drugs interacting with enzymes. Update 2014
W Froestl, A Muhs, A Pfeifer - Journal of Alzheimer's Disease, 2014 - content.iospress.com
Scientists working in the field of Alzheimer's disease and, in particular, cognitive enhancers
are very productive. The review on Drugs interacting with Enzymes was accepted in August …
are very productive. The review on Drugs interacting with Enzymes was accepted in August …
Magnetically Separable Copper Ferrite Nanoparticles‐Catalyzed Synthesis of Diaryl, Alkyl/Aryl Sulfones from Arylsulfinic Acid Salts and Organohalides/Boronic Acids
BTV Srinivas, VS Rawat, K Konda… - Advanced Synthesis & …, 2014 - Wiley Online Library
A recyclable, inexpensive, non‐toxic and environmentally benign catalytic system comprised
of magnetically separable copper ferrite (CuFe2O4) nanoparticles has been developed for …
of magnetically separable copper ferrite (CuFe2O4) nanoparticles has been developed for …
An efficient tandem aldol condensation-thia-Michael addition process
MS Abaee, S Cheraghi, S Navidipoor, MM Mojtahedi… - Tetrahedron …, 2012 - Elsevier
An efficient synthesis of β-aryl-β-mercapto ketones is achieved via a tandem aldol
condensation-thia-Michael addition process using an aqueous medium and diethylamine …
condensation-thia-Michael addition process using an aqueous medium and diethylamine …
Discovery of brain permeable 2-Azabicyclo [2.2. 2] octane sulfonamides as a novel class of presenilin-1 selective γ-secretase inhibitors
R Narlawar, L Serneels, C Gaffric, HJM Gijsen… - European Journal of …, 2023 - Elsevier
This paper describes the rational design, synthesis, structure-activity relationship (SAR), and
biological profile of presenilin-1 (PSEN-1) complex selective γ-secretase inhibitors …
biological profile of presenilin-1 (PSEN-1) complex selective γ-secretase inhibitors …
[HTML][HTML] Synthesis, characterization and catalytic evaluation of ZrCl4: Mg (ClO4) 2 for the synthesis of 1, 3-diaryl-3-(phenylthio) propan-1-one
Herein we demonstrate a novel tandem aldol condensation-thia-Michael addition process
using a bimetallic catalyst (ZrCl 4: Mg (ClO 4) 2). The novel bimetallic catalyst performs …
using a bimetallic catalyst (ZrCl 4: Mg (ClO 4) 2). The novel bimetallic catalyst performs …
Discovery of a novel, potent spirocyclic series of γ-secretase inhibitors
Z Zhao, DA Pissarnitski, HB Josien… - Journal of Medicinal …, 2015 - ACS Publications
In the present paper, we described the design, synthesis, SAR, and biological profile of a
novel spirocyclic sulfone series of γ-secretase inhibitors (GSIs) related to MRK-560. We …
novel spirocyclic sulfone series of γ-secretase inhibitors (GSIs) related to MRK-560. We …
Cognitive enhancers (nootropics). Part 2: drugs interacting with enzymes
W Froestl, A Muhs, A Pfeifer - Journal of Alzheimer's Disease, 2013 - content.iospress.com
Cognitive enhancers (nootropics) are drugs to treat cognition deficits in patients suffering
from Alzheimer's disease, schizophrenia, stroke, attention deficit hyperactivity disorder, or …
from Alzheimer's disease, schizophrenia, stroke, attention deficit hyperactivity disorder, or …
Tricyclic sulfones as orally active γ-secretase inhibitors: Synthesis and structure–activity relationship studies
TK Sasikumar, L Qiang, DA Burnett, D Cole… - Bioorganic & medicinal …, 2010 - Elsevier
Tricyclic sulfones were designed as γ-secretase inhibitors and found to have excellent
potency. Extensive SAR shows that a large number of sulfonamides at position 7 of the …
potency. Extensive SAR shows that a large number of sulfonamides at position 7 of the …
Discovery of SCH 900229, a potent presenilin 1 selective γ-secretase inhibitor for the treatment of alzheimer's disease
WL Wu, M Domalski, DA Burnett, H Josien… - ACS Medicinal …, 2012 - ACS Publications
An exploration of the SAR of the side chain of a novel tricyclic series of γ-secretase inhibitors
led to the identification of compound (−)-16 (SCH 900229), which is a potent and PS1 …
led to the identification of compound (−)-16 (SCH 900229), which is a potent and PS1 …