Recent advances in biological active sulfonamide based hybrid compounds Part A: Two-component sulfonamide hybrids

R Ghomashi, S Ghomashi, H Aghaei… - Current Medicinal …, 2023 - ingentaconnect.com
Sulfonamides constitute an important class of drugs, with many types of pharmacological
agents possessing antibacterial, anti-carbonic anhydrase, anti-obesity, diuretic …

Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review

A Bendi, Taruna, Rajni, S Kataria, L Singh… - Archiv der …, 2024 - Wiley Online Library
Nowadays, the scientific community has focused on dealing with different kinds of diseases
by exploring the chemistry of various heterocycles as novel drugs. In this connection …

Synthesis and biological evaluation of coumarin‐thiazole hybrids as selective carbonic anhydrase IX and XII inhibitors

PS Thacker, V Newaskar, A Angeli… - Archiv der …, 2022 - Wiley Online Library
A series of coumarin‐linked thiazoles (6a–p) was synthesized and the synthesized
compounds were evaluated against human carbonic anhydrases (hCAs) IX and XII, which …

Design, synthesis, and in vitro and in silico studies of morpholine derived thiazoles as bovine carbonic anhydrase-II inhibitors

M Tasleem, S Ullah, A Khan, SN Mali, S Kumar… - RSC …, 2024 - pubs.rsc.org
Carbonic anhydrase CA-II enzyme is essential for maintaining homeostasis in several
processes, including respiration, lipogenesis, gluconeogenesis, calcification, bone …

Synthesis, characterization, carbonic anhydrase inhibitor activity, and docking studies of phenylthiazol-2 (3h)-ylidene-isoquinoline-5-amine Derivatives

N Berber, AS Şahutoğlu, B Gökçe, K Çıkrıkçı… - Journal of Molecular …, 2023 - Elsevier
Abstract Phenylthiazol-2 (3h)-ylidene-isoquinoline-5-amine derivatives (5a-r) were easily
prepared from 5-aminoisoquinoline, thioisocyanate, and phenacyl bromide derivatives in the …

Synthesis of 4-hydroxy-L-proline derivatives as new non-classical inhibitors of human carbonic anhydrase II activity: an in vitro study

L Moghoufei, M Mehrabi, H Adibi… - Journal of Biomolecular …, 2023 - Taylor & Francis
Carbonic anhydrase (CA) is a zinc metalloenzyme that facilitates the rapid conversion of
water and carbon dioxide into proton and bicarbonate ion. CA isozymes have been broadly …

Synthesis, Characterization, and Study of Anticancer Activities of New Schiff Bases and 1, 3-Oxazepine Containing Drug

RA Ali, LS Ahamed, SIC AL-Khazraji - Russian Journal of Bioorganic …, 2024 - Springer
Objective: This study involved the synthesis of new Schiff bases and 1, 3-oxazepine
derivatives from the baclofen drug and study the anticancer activities. Methods: Baclofen …

Synthesis and Identification of Some New Heterocyclic Compounds Derived from N-(6-Hydrazinyl-6-oxohexanoyl)phthalimide

RA Ali, EO Al-Tamimi, ZG Alrecabi - Russian Journal of Organic Chemistry, 2024 - Springer
New substituted heterocyclic compounds 2a–2c were synthesized from N-(6-hydrazinyl-6-
oxohexanoyl) phthalimide, and their structure was confirmed by FT-IR, 1H NMR, and 13C …

Synthesis and Characterization of Thiazole Compounds in the Presence of Various Reagents, Catalysts and Solvents

N Berber - Sakarya University Journal of Science, 2022 - dergipark.org.tr
The reaction medium plays a key role in organic synthesis and pharmaceutical research.
There are many opinions on choosing the best condition, including cost and environmental …

Benzotiyazol türevi kalkonların sentezi, biyolojik aktivite, teorik hesaplama ve moleküler yerleştirme çalışmaları= Synthesis, biological activity, theoretical calculation …

AB Musatat - 2023 - acikerisim.sakarya.edu.tr
Flavonoid ailesinin üyeleri çok çeşitli biyolojik aktivitelere sahiptir ve doğal bileşiklerin bu
grubu meyveler, bitkiler, tohumlar, yapraklar ve birçok çiçekte bulunmaktadır. Doğal veya …