Evaluation of new chalcone derivatives as polyphenol oxidase inhibitors

F Sonmez, S Sevmezler, A Atahan, M Ceylan… - Bioorganic & medicinal …, 2011 - Elsevier
A newly series of 4-(phenylurenyl) chalcone (4a–j) and 4′-(phenylurenyl/thiourenyl)
chalcone (9a–l) derivatives were synthesized and their inhibitory effects on the diphenolase …

Rational design and multibiological profiling of novel donepezil–trolox hybrids against Alzheimer's disease, with cholinergic, antioxidant, neuroprotective, and …

P Cai, SQ Fang, XL Yang, JJ Wu, QH Liu… - ACS Chemical …, 2017 - ACS Publications
A novel series of donepezil-trolox hybrids were designed, synthesized, and evaluated as
multifunctional ligands against Alzheimer's disease (AD). Biological assays showed that …

New saccharin derivatives as tyrosinase inhibitors

N Gençer, D Demir, F Sonmez… - Bioorganic & medicinal …, 2012 - Elsevier
A newly series of 6-(phenylurenyl/thiourenyl) saccharin (6a–y) derivatives were synthesized
and their inhibitory effects on the diphenolase activity of banana tyrosinase were evaluated …

1, 3, 4-Oxadiazole-3 (2H)-carboxamide derivatives as potential novel class of monoamine oxidase (MAO) inhibitors: Synthesis, evaluation, and role of urea moiety

S Ke, Z Li, X Qian - Bioorganic & medicinal chemistry, 2008 - Elsevier
A new series of 1, 3, 4-oxadiazole-3 (2H)-carboxamide derivatives have been synthesized
by direct heterocyclization reaction of substituted benzoylisocyanate with various …

1, 3, 4-Oxadiazoline derivatives as novel potential inhibitors targeting chitin biosynthesis: Design, synthesis and biological evaluation

S Ke, F Liu, N Wang, Q Yang, X Qian - Bioorganic & Medicinal Chemistry …, 2009 - Elsevier
Two series of 1, 3, 4-oxadiazoline heterocycle derivatives were designed, synthesized and
identified. Bioactivity assays showed that all synthesized compounds inhibited chitin …

In vitro inhibition effect of some chalcones on erythrocyte carbonic anhydrase I and II

N Gençer, Ç Bilen, D Demir, A Atahan… - Artificial Cells …, 2013 - Taylor & Francis
Abstract In this study, 4'-(phenylurenyl/thiourenyl) chalcones (14–25) were prepared from 4'-
(phenylurenyl/thiourenyl) acetophenones and benzaldehyde derivatives by Claisen-Schmidt …

Facile synthesis of dithiatetraaza-macrocycles of potential anti-inflammatory activity

AS Girgis - European journal of medicinal chemistry, 2008 - Elsevier
A facile synthetic approach towards dithiatetraaza-macrocycles 4a and b was achieved
through reaction of 2, 2′-[alkanediylbis (thio)] bisbenzenamines 1a and b with 1, 4 …

New Quinoxaline Derivatives as Potential MT1 and MT2 Receptor Ligands

S Ancizu, N Castrillo, S Pérez-Silanes, I Aldana… - Molecules, 2012 - mdpi.com
Ever since the idea arose that melatonin might promote sleep and resynchronize circadian
rhythms, many research groups have centered their efforts on obtaining new melatonin …

Solvent-controlled synthesis of bulky and polar-bulky galactonoamidines

S Striegler, I Orizu - Carbohydrate Research, 2022 - Elsevier
The goal of this study was the design and synthesis of bulky and polar-bulky
galactonoamidines that have a potential to interact with both catalytic amino acids in the …

Building a MCHR1 homology model provides insight into the receptor–antagonist contacts that are important for the development of new anti-obesity agents

N Cirauqui, AK Schrey, S Galiano, J Ceras… - Bioorganic & medicinal …, 2010 - Elsevier
Melanin-concentrating hormone (MCH) regulates feeding and energy homeostasis through
interaction with its receptor, the melanin-concentrating receptor 1 (MCHR1), making it a …