Identification and synthesis of selective cholesterol esterase inhibitor using dynamic combinatorial chemistry

S Zhao, Y Wu, L Hu - Bioorganic Chemistry, 2022 - Elsevier
In this study, the concept of dynamic combinatorial chemistry (DCC) was applied to explore
novel cholesterol esterase (CEase) inhibitors. In the presence of enzyme, two substrates …

Synthesis and biological evaluation of phosphorylated flavonoids as potent and selective inhibitors of cholesterol esterase

Y Wei, AY Peng, B Wang, L Ma, G Peng, Y Du… - European Journal of …, 2014 - Elsevier
A series of phosphorylated flavonoids were synthesized and investigated in vitro as
inhibitors of pancreatic cholesterol esterase (CEase) and acetylcholinesterase (AChE). The …

Benzoflavones as cholesterol esterase inhibitors: Synthesis, biological evaluation and docking studies

H Singh, JV Singh, MK Gupta, P Singh… - Bioorganic & Medicinal …, 2017 - Elsevier
Abstract A library of forty 7, 8-benzoflavone derivatives was synthesized and evaluated for
their inhibitory potential against cholesterol esterase (CEase). Among all the synthesized …

Molecular docking of different inhibitors and activators to butyrylcholinesterase

SY Chiou, TT Weng, GZ Lin, RJ Lu… - Journal of Biomolecular …, 2015 - Taylor & Francis
There are three major active sites of butyrylcholinesterase: catalytic site, peripheral site, and
activator site. In this study, pseudosubstrate inhibitors, 1, 3, 5-alkylcarbamyloxybenzenes (1 …

Synthesis and evaluation of 2-(1H-indol-3-yl)-4-phenylquinolines as inhibitors of cholesterol esterase

GC Muscia, S Hautmann, GY Buldain, SE Asís… - Bioorganic & Medicinal …, 2014 - Elsevier
Abstract A series of 2-(substituted) phenyl and 2-indolyl quinoline derivatives (10a–l) was
synthesized by an efficient microwave-assisted, trifluoroacetic acid-catalyzed, solvent-free …

Systems biology approach deciphering the biochemical signaling pathway and pharmacokinetic study of PI3K/mTOR/p53-Mdm2 module involved in neoplastic …

D Arora, A Singh - Network Modeling Analysis in Health Informatics and …, 2018 - Springer
Cancer is a serious health concern growing at a rapid speed where normal cells take
neoplastic transformation. Different pathway is tightly regulated with each other to maintain …

ω‐Phthalimidoalkyl Aryl Ureas as Potent and Selective Inhibitors of Cholesterol Esterase

FM Dato, M Sheikh, RZ Uhl, AW Schüller… - …, 2018 - Wiley Online Library
Cholesterol esterase (CEase), a serine hydrolase thought to be involved in atherogenesis
and thus coronary heart disease, is considered as a target for inhibitor development. We …

Microwave-assisted SiO2-H2SO4-catalyzed Synthesis of 3,4,6,7-Tetrahydro-3,3,6,6-tetramethyl-9,10- diphenylacridine-1,8-dione Derivatives as Cholesterol …

H Singh, A Singh, MK Gupta… - Indian Journal of …, 2017 - search.ebscohost.com
Abstract A library of 3, 4, 6, 7-tetrahydro-3, 3, 6, 6-tetramethyl-9, 10-diphenylacridine-1, 8-
dione derivatives were synthesized via microwave-assisted three-component reaction …

5, 6-Benzoflavones as cholesterol esterase inhibitors: synthesis, biological evaluation and docking studies

JV Singh, A Kaur, K Bhagat, MK Gupta, M Singh… - …, 2018 - pubs.rsc.org
In a continued effort to develop potent cholesterol esterase (CEase) inhibitors, a series of 5,
6-benzoflavone derivatives was rationally designed and synthesized by changing the …

[PDF][PDF] SÍNTESE DE ÉSTERES A PARTIR DE ÁCIDOS GRAXOS E FENÓIS PARA APLICAÇÃO COMO TENSOATIVOS NA INDÚSTRIA DE PETRÓLEO

TDEO SANTOS - uesb.br
No presente trabalho sintetizou-se ésteres graxos derivados de ácidos graxos naturais e
fenóis com o objetivo de se obter novos tensoativos biodegradáveis e biocompatíveis. A …