Synthesis and reactivity of propargylamines in organic chemistry
K Lauder, A Toscani, N Scalacci… - Chemical reviews, 2017 - ACS Publications
Propargylamines are a versatile class of compounds which find broad application in many
fields of chemistry. This review aims to describe the different strategies developed so far for …
fields of chemistry. This review aims to describe the different strategies developed so far for …
“Click Chemistry”: An Emerging Tool for Develo** a New Class of Structural Motifs against Various Neurodegenerative Disorders
A Manoharan, J Jayan, TM Rangarajan, K Bose… - ACS …, 2023 - ACS Publications
Click chemistry is a set of easy, atom-economical reactions that are often utilized to combine
two desired chemical entities. Click chemistry accelerates lead identification and …
two desired chemical entities. Click chemistry accelerates lead identification and …
Monoamine oxidase‐B inhibitors as potential neurotherapeutic agents: An overview and update
RKP Tripathi, SR Ayyannan - Medicinal research reviews, 2019 - Wiley Online Library
Monoamine oxidase (MAO) inhibitors have made significant contributions and remain an
indispensable approach of molecular and mechanistic diversity for the discovery of …
indispensable approach of molecular and mechanistic diversity for the discovery of …
Pathogenesis of Alzheimer's Disease and Diversity of 1, 2, 3-Triazole Scaffold in Drug Development: Design Strategies, Structural Insights, and Therapeutic Potential
Alzheimer's disease is a most prevalent form of dementia all around the globe and currently
poses a significant challenge to the healthcare system. Currently available drugs only slow …
poses a significant challenge to the healthcare system. Currently available drugs only slow …
Identifying natural compounds as multi-target-directed ligands against Alzheimer's disease: an in silico approach
Alzheimer's disease (AD) is a multi-factorial disease, which can be simply outlined as an
irreversible and progressive neurodegenerative disorder with an unclear root cause. It is a …
irreversible and progressive neurodegenerative disorder with an unclear root cause. It is a …
Propargylamine-derived multi-target directed ligands for Alzheimer's disease therapy
M do Carmo Carreiras, L Ismaili… - Bioorganic & Medicinal …, 2020 - Elsevier
Current options for the treatment of Alzheimeŕs disease have been restricted to prescription
of acetylcholinesterase inhibitors or N-methyl-d-aspartate receptor antagonist, memantine …
of acetylcholinesterase inhibitors or N-methyl-d-aspartate receptor antagonist, memantine …
Challenging the anticolorectal cancer capacity of quinoxaline-based scaffold via triazole ligation unveiled new efficient dual VEGFR-2/MAO-B inhibitors
Monoamine oxidases (MAOs) and vascular endothelial growth factor receptor-2 (VEGFR-2)
are promoters of colorectal cancer (CRC) and central signaling nodes in epithelial …
are promoters of colorectal cancer (CRC) and central signaling nodes in epithelial …
Design, synthesis and evaluation of coumarin-pargyline hybrids as novel dual inhibitors of monoamine oxidases and amyloid-β aggregation for the treatment of …
HL Yang, P Cai, QH Liu, XL Yang, F Li, J Wang… - European Journal of …, 2017 - Elsevier
A series of coumarin-pargyline hybrids (4a-x) have been designed, synthesized and
evaluated as novel dual inhibitors of Alzheimer's disease (AD). Most of the compounds …
evaluated as novel dual inhibitors of Alzheimer's disease (AD). Most of the compounds …
Monoamine oxidase A and B inhibitory activities of 3, 5-diphenyl-1, 2, 4-triazole substituted [1, 2, 4] triazolo [3, 4-b][1, 3, 4] thiadiazole derivatives
Abstract Monoamine oxidase (EC 1.4. 3.4, MAO) is a flavin adenine dinucleotide-containing
flavoenzyme located on the outer mitochondrial membrane and catalyzes the oxidative …
flavoenzyme located on the outer mitochondrial membrane and catalyzes the oxidative …
Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
DV Reshetnikov, ID Ivanov, DS Baev, TV Rybalova… - Molecules, 2022 - mdpi.com
Xanthine derivatives have been a great area of interest for the development of potent
bioactive agents. Thirty-eight methylxanthine derivatives as acetylcholinesterase inhibitors …
bioactive agents. Thirty-eight methylxanthine derivatives as acetylcholinesterase inhibitors …