Recent advances in intestinal alkaline phosphatase, inflammation, and nutrition

JP Lallès - Nutrition reviews, 2019 - academic.oup.com
In recent years, much new data on intestinal alkaline phosphatase (IAP) have been
published, and major breakthroughs have been disclosed. The aim of the present review is …

TNAP as a therapeutic target for cardiovascular calcification: a discussion of its pleiotropic functions in the body

C Goettsch, A Strzelecka-Kiliszek… - Cardiovascular …, 2022 - academic.oup.com
Cardiovascular calcification (CVC) is associated with increased morbidity and mortality. It
develops in several diseases and locations, such as in the tunica intima in atherosclerosis …

Photoredox Cyclization of N-Arylacrylamides for Synthesis of Dihydroquinolinones

Z Liu, S Zhong, X Ji, GJ Deng, H Huang - Organic Letters, 2021 - ACS Publications
Metal-and additive-free photoredox cyclization of N-arylacrylamides is herein reported that
provides a concise access to the formation of dihydroquinolinones. In this protocol …

Emodin Inhibits the proliferation of MCF-7 human breast cancer cells through activation of aryl hydrocarbon receptor (AhR)

N Zhang, J Wang, A Sheng, S Huang, Y Tang… - Frontiers in …, 2021 - frontiersin.org
Natural products have proved to be a promising source for the development of potential
anticancer drugs. Emodin, a natural compound from Rheum palmatum, is used to treat …

Current status of N-, O-, S-heterocycles as potential alkaline phosphatase inhibitors: a medicinal chemistry overview

RS Jassas, N Naeem, A Sadiq, R Mehmood… - RSC …, 2023 - pubs.rsc.org
Heterocycles are a class of compounds that have been found to be potent inhibitors of
alkaline phosphatase (AP), an enzyme that plays a critical role in various physiological …

2-Benzylidenebenzofuran-3 (2 H)-ones as a new class of alkaline phosphatase inhibitors: synthesis, SAR analysis, enzyme inhibitory kinetics and computational …

J Ashraf, EU Mughal, RI Alsantali, A Sadiq, RS Jassas… - RSC …, 2021 - pubs.rsc.org
The excelling role of organic chemistry in the medicinal field continues to be one of the main
leads in the drug development process. Particularly, this industry requires organic chemists …

Current updates on green synthesis and biological properties of 4-quinolone derivatives

S Jaiswal, N Arya, N Yaduvanshi, M Devi, S Jain… - Journal of Molecular …, 2023 - Elsevier
The chemistry of quinolones, representing one of the major classes of nitrogen-containing
heterocyclics, has received more attention and considered one of the promising …

Trending strategies for the synthesis of quinolinones and isoquinolinones

LB Rao, C Sreenivasulu, DR Kishore… - Tetrahedron, 2022 - Elsevier
Heterocyclic compounds are indispensable structures that have widespread occurrence in
nature and exhibit fascinating biological and pharmaceutical activities. Particularly …

Hypervalent iodine (III)-promoted C3–H regioselective halogenation of 4-quinolones under mild conditions

F Yang, X Wang, W Zhao, F Yu, Z Yu - ACS omega, 2021 - ACS Publications
A simple and practical protocol for the C3–H regioselective halogenation of 4-quinolones by
the action of potassium halide salt and PIFA/PIDA in good to excellent yields was …

Synthesis of sulfadiazinyl acyl/aryl thiourea derivatives as calf intestinal alkaline phosphatase inhibitors, pharmacokinetic properties, lead optimization, Lineweaver …

A Saeed, G Saddique, PA Channar, FA Larik… - Bioorganic & Medicinal …, 2018 - Elsevier
To seek the new medicinal potential of sulfadiazine drug, the free amino group of
sulfadiazine was exploited to obtain acyl/aryl thioureas using simple and straightforward …