Pyrazolone structural motif in medicinal chemistry: Retrospect and prospect

Z Zhao, X Dai, C Li, X Wang, J Tian, Y Feng… - European journal of …, 2020 - Elsevier
The pyrazolone structural motif is a critical element of drugs aimed at different biological end-
points. Medicinal chemistry researches have synthesized drug-like pyrazolone candidates …

Biological aspects of Schiff base–metal complexes derived from benzaldehydes: an overview

RK Mohapatra, PK Das, MK Pradhan… - Journal of the Iranian …, 2018 - Springer
Schiff bases are stable imines containing C= N, where N is bonded to an alkyl or aryl group,
but not with hydrogen and are prepared by condensation of aliphatic or aromatic primary …

Synthesis and biological evaluation of new pyrazolone Schiff bases as monoamine oxidase and cholinesterase inhibitors

F Tok, B Koçyiğit-Kaymakçıoğlu, BN Sağlık, S Levent… - Bioorganic …, 2019 - Elsevier
In the current work, Schiff base derivatives of antipyrine were synthesized. The chemical
characterization of the compounds was confirmed using IR, 1 H NMR, 13 C NMR and mass …

2ʹ-Aryl and 4ʹ-arylidene substituted pyrazolones: As potential α-amylase inhibitors

S Yousuf, KM Khan, U Salar, S Chigurupati… - European journal of …, 2018 - Elsevier
Acarbose and voglibose are well-known α-amylase inhibitors used for the management of
type-II diabetes mellitus. Unfortunately, these well-known and clinically used inhibitors are …

Potent and selective carbonic anhydrase inhibition activities of pyrazolones bearing benzenesulfonamides

S Akocak, N Lolak, S Giovannuzzi… - Bioorganic & Medicinal …, 2023 - Elsevier
This research introduces a series of fourteen 4-aryl-hydrazonopyrazolone sulfonamide
derivatives, denoted as 3 (ag) and 4 (ag), which encompass various aromatic substitutions …

Indole-3-acetamides: As potential antihyperglycemic and antioxidant agents; synthesis, in vitro α-amylase inhibitory activity, structure–activity relationship, and in silico …

Kanwal, KM Khan, S Chigurupati, F Ali, M Younus… - ACS …, 2021 - ACS Publications
Indole-3-acetamides (1–24) were synthesized via coupling of indole-3-acetic acid with
various substituted anilines in the presence of coupling reagent 1, 1-carbonyldiimidazole …

Substituted benzimidazole analogues as potential α-amylase inhibitors and radical scavengers

AA Akande, U Salar, KM Khan, S Syed, SA Aboaba… - ACS …, 2021 - ACS Publications
Benzimidazole scaffolds are known to have a diverse range of biological activities and found
to be antidiabetic and antioxidant. In this study, a variety of arylated benzimidazoles 1–31 …

Biology-oriented synthesis (BIOS) of piperine derivatives and their comparative analgesic and antiinflammatory activities

A Yasir, S Ishtiaq, M Jahangir, M Ajaib… - Medicinal …, 2018 - ingentaconnect.com
Background: Serious side effects such as gastric intestinal ulcer, bleeding etc. are
associated with most of the antiinflammatory and analgesic drugs. So, there is a need to …

Evaluation of S-substituted-2-mercaptobenzimidazole analogs for urease inhibitory and DPPH radical scavenging potential: synthesis, bioactivity, and molecular …

A Ata, KM Khan, M Lateef, U Salar, A Anwar… - Journal of the Iranian …, 2023 - Springer
Abstract Several S-substituted-2-mercaptobenzimidazole derivatives 1–34 were synthesized
by reacting 2-mercaptobenzimidazole with a variety of substituted benzyl bromide and …

[PDF][PDF] Biological evaluation of aromatic bis-sulfonamide Schiff bases as antioxidant, acetylcholinesterase and butyrylcholinesterase inhibitors

N Lolak, S Akocak - Cumhuriyet Science Journal, 2020 - dergipark.org.tr
Aromatic/heterocyclic Schiff bases are one of the most investigated and studied scaffold for
many pharmaceutical applications. For this reason, in the current work, a series of aromatic …