Arylsulfonamides and selectivity of matrix metalloproteinase-2: An overview

N Adhikari, A Mukherjee, A Saha, T Jha - European Journal of Medicinal …, 2017 - Elsevier
Uncontrolled regulation of specific metalloenzymes plays important roles in several
diseases like tumor metastasis and inflammation. Therefore, selective metalloenzyme …

Synthesis, characterization and antimicrobial activity of new aliphatic sulfonamide

N Özbek, H Katırcıoğlu, N Karacan, T Baykal - Bioorganic & medicinal …, 2007 - Elsevier
A series of novel aliphatic sulfonamide derivatives (1–7) were synthesized and
characterized by elemental analyses, FT-IR, 1H NMR, 13C NMR and LC–MS techniques. All …

Molecular docking and investigation of 4-(benzylideneamino)-and 4-(benzylamino)-benzenesulfonamide derivatives as potent AChE inhibitors

M Işık, Y Demir, M Durgun, C Türkeş, A Necip… - Chemical Papers, 2020 - Springer
The discovery of acetylcholinesterase inhibitors is important for the treatment of Alzheimer's
disease (AD), known as the most common type of dementia. Due to the side effects of …

Role of sulfonamide group in matrix metalloproteinase inhibitors

XC Cheng, Q Wang, H Fang… - Current medicinal …, 2008 - ingentaconnect.com
Sulfonamide hydroxamates were designed and synthesized as efficient matrix
metalloproteinase (MMP) inhibitors since the discovery of CGS 27023A in 1994. The …

New sulfonamide derivatives based on 1,2,3-triazoles: synthesis, in vitro biological activities and in silico studies

İ Şahin, M Çeşme, Ö Güngör, FB Özgeriş… - Journal of …, 2024 - Taylor & Francis
Eight new hybrid constructs containing a series of sulfonamide and 1, 2, 3-triazole units
were designed and synthesized. Anticancer, antioxidant and cholinesterase activities of …

Profiling of alterations in platelet proteins during storage of platelet concentrates

T Thiele, L Steil, S Gebhard, C Scharf, E Hammer… - …, 2007 - Wiley Online Library
BACKGROUND: The quality of platelet concentrates (PCs) is primarily determined in vitro by
selective methods (eg, pH, aggregometry), which provide only limited information on certain …

Highly Potent and Selective Dopamine D4 Receptor Antagonists Potentially Useful for the Treatment of Glioblastoma

P Pavletic, A Semeano, H Yano… - Journal of medicinal …, 2022 - ACS Publications
To better understand the role of dopamine D4 receptor (D4R) in glioblastoma (GBM), in the
present paper, new ligands endowed with high affinity and selectivity for D4R were …

Molecular docking and inhibition of matrix metalloproteinase-2 by novel difluorinatedbenzylidene curcumin analog

A Ahmad, A Sayed, KR Ginnebaugh… - American journal of …, 2015 - pmc.ncbi.nlm.nih.gov
We recently described the synthesis and characterization of a novel
difluorinatedbenzylidene analog of curcumin, commonly referred as CDF, which …

Design, synthesis and antimalarial activity of benzene and isoquinoline sulfonamide derivatives

MK Parai, G Panda, K Srivastava, SK Puri - Bioorganic & medicinal …, 2008 - Elsevier
A new series of benzene and isoquinoline sulfonamide derivatives were synthesized by
nucleophilic displacement reaction on benzene and isoquinoline sulfonyl chlorides by …

Insight into the structural requirements of gelatinases (MMP-2 and MMP-9) inhibitors by multiple validated molecular modelling approaches: Part II

S Das, SA Amin, S Gayen, T Jha - SAR and QSAR in …, 2022 - Taylor & Francis
Inhibition of the matrix metalloproteinases (MMPs) is effective against metastasis of
secondary tumours. Previous MMP inhibitors have failed in clinical trials due to their off …