Carbonic anhydrase inhibitors (CAIs) are of growing interest since various isoforms of the enzyme are identified as promising drug targets for treatment of disease. The principal …
G Vannozzi, D Vullo, A Angeli, M Ferraroni… - Journal of Medicinal …, 2021 - ACS Publications
We report a one-pot procedure for the synthesis of asymmetrical ureido-containing benzenesulfonamides based on in situ generation of the corresponding …
AV Chate, PK Bhadke, MA Khande… - Chinese Chemical …, 2017 - Elsevier
An efficient and green method has been developed for the synthesis of 2H-indazolo [2, 1-b] phthalazine-triones derivatives by employing 15 mol% β-cyclodextrinvia a one-pot …
N Naeem, A Sadiq, GA Othman, HM Yassin… - RSC Advances, 2024 - pubs.rsc.org
Heterocyclic compounds represent a prominent class of molecules with diverse pharmacological activities. Among their therapeutic applications, they have gained …
SZ Mostashari, A Fallah Shojaei… - Research on Chemical …, 2022 - Springer
Abstract Fe 3 O 4@ SiO 2-(CH 2) 3-NH-Asn-Cu (II) was synthesized via functionalization of synthesized Fe 3 O 4 with 3-aminopropyltriethoxysilane, asparagine, and Cu (OAc) 2. The …
A series of novel tetrahydroquinoline derivatives containing urea moiety was synthesized and their in vitro inhibitory effects on the human carbonic anhydrase isoenzymes (hCA− I …
Abstract Phenylthiazol-2 (3h)-ylidene-isoquinoline-5-amine derivatives (5a-r) were easily prepared from 5-aminoisoquinoline, thioisocyanate, and phenacyl bromide derivatives in the …
Fourteen phthalazine-triones bearing different substituents at C-4 position were synthesized through multicomponent reactions (MCR) by using phthalhydrazide, dimedone and diferent …
The application of nitrogen-containing heterocyclic molecules in many fields, such as pharmaceuticals, has gotten a lot of interest. Phthalazine and its oxygenated derivatives …