New isoindole‐1, 3‐dione substituted sulfonamides as potent inhibitors of carbonic anhydrase and acetylcholinesterase: Design, synthesis, and biological evaluation

S Gündoğdu, C Türkeş, M Arslan, Y Demir… - …, 2019 - Wiley Online Library
Herein, a series of isoindole‐1, 3‐dione substituted sulfonamide derivatives (3, 4 a–k) were
designed, synthesized, and biologically evaluated, as inhibitors of carbonic anhydrase (CA) …

Synthesis, Antimicrobial, Antiquorum‐Sensing, and Cytotoxic Activities of New Series of Isoindoline‐1,3‐dione, Pyrazolo[5,1‐a]isoindole, and Pyridine Derivatives

NS El‐Gohary, MI Shaaban - Archiv der Pharmazie, 2015 - Wiley Online Library
New series of isoindoline‐1, 3‐diones 2–9, pyrazolo [5, 1‐a] isoindoles 10–14, and
pyridines 16–18 were synthesized. Twenty of the synthesized compounds were screened for …

Design and synthesis of novel tetrabromophthalimide derivatives as potential tubulin inhibitors endowed with apoptotic induction for cancer treatment

M Abdel‐Motaal, DA Aldakhili… - Drug Development …, 2024 - Wiley Online Library
Although various approaches exist for treating cancer, chemotherapy continues to hold a
prominent role in the management of this disease. Besides, microtubules serve as a vital …

Synthesis, anti-inflammatory, and antiproliferative activity evaluation of isoindole, pyrrolopyrazine, benzimidazoisoindole, and benzimidazopyrrolopyrazine derivatives

S Kumar, N Kumar, P Roy, SM Sondhi - Molecular diversity, 2013 - Springer
A number of isoindole (3x, 3y, 6xa–6ye), pyrrolopyrazine (3z, 6za–6ze),
benzimidazoisoindole (4x, 4y, 7xa–7ye), and benzimidazopyrrolopyrazine (4z, 7za–7ze) …

Isoindoline derivatives of α‐amino acids as cyclooxygenase 1 and 2 inhibitors

T Mancilla‐Percino, CR Trejo‐Muñoz… - Archiv der …, 2016 - Wiley Online Library
IC50 values were obtained for two series of isoindolines derived from α‐amino acids over
cyclooxygenase 1 and 2 (COX‐1 and COX‐2). In order to explain the biological activity …

Anti-inflammatory aminoacetylenic isoindoline-1, 3-dione derivatives modulate cytokines production from different spleen cell populations

KZ Matalka, F Alfarhoud, NA Qinna, EM Mallah… - International …, 2012 - Elsevier
We recently designed a series of N-[4-(t-amino-yl)-but-2-yn-1-yl] isoindoline-1, 3-diones as
anti-inflammatory compounds, called ZM compounds. These ZM compounds were …

Analgesic and Toxicity Studies of Aminoacetylenic Isoindoline‐1, 3‐dione Derivatives

R Shakir, ZA Muhi-Eldeen, KZ Matalka… - International …, 2012 - Wiley Online Library
We have developed a series of aminoacetylenic isoindoline‐1, 3‐dione compounds and
showed their anti‐inflammatory activities by reducing carrageenan‐induced rat paw edema …

A Garratt-Braverman route to isoindolines and phthalans

M Singha, M Maji, M Gupta, S Majhi, A Basak - Tetrahedron Letters, 2019 - Elsevier
Abstract Garratt-Braverman (GB) cyclization, two Csingle bondC bond forming reaction in a
single step, has been utilized to construct several isoindoline and phthalan derivatives. The …

Grinding and Microwave‐assisted Synthesis of Heterocyclic Molecules in High Yields and Their Biological Evaluation

S Kumar, A Kumar, N Kumar, P Roy… - Journal of Heterocyclic …, 2016 - Wiley Online Library
Cis‐cyclohexane1, 2‐dicarboxylic acid (1a), phthalic acid (1b), and pyrazine 2, 3‐
dicarboxylic acid (1c) on grinding with hydrazine hydrate (2a) gave 2‐aminohexahydro‐1H …

Estrategias de desplazamiento de Ateles geoffroyi yucatanensis y Alouatta pigra en la búsqueda de recursos tróficos durante la temporada seca y húmeda en la …

M en Neuroetología - 2013 - sii.ecosur.mx
UNIVERSIDAD VERACRUZANA Instituto de Neuroetología Estrategias de desplazamiento de
Ateles geoffroyi yucatanensis y Alouatta pi Page 1 UNIVERSIDAD VERACRUZANA Instituto …