Carbonic anhydrase IX: A tumor acidification switch in heterogeneity and chemokine regulation

A Queen, HN Bhutto, M Yousuf, MA Syed… - Seminars in Cancer …, 2022 - Elsevier
The primary physiological process of respiration produces carbon dioxide (CO 2) that reacts
with water molecules which subsequently liberates bicarbonate (HCO–3) and protons …

A novel series of thiosemicarbazone hybrid scaffolds: Design, synthesis, DFT studies, metabolic enzyme inhibition properties, and molecular docking calculations

H Yakan, H Muğlu, C Türkeş, Y Demir… - Journal of Molecular …, 2023 - Elsevier
The fourteen new thiosemicarbazone derivatives of Schiff base were synthesized from the
condensation reactions of two different aldehydes (3‑hydroxy-4-methoxhybenzaldehyde and …

Naringenin as a potential inhibitor of human cyclin-dependent kinase 6: Molecular and structural insights into anti-cancer therapeutics

M Yousuf, A Shamsi, S Khan, P Khan… - International Journal of …, 2022 - Elsevier
Cancer is one of the major causes of global deaths and needs immediate therapeutic
development. So far, several strategies have been undertaken to prevent cancer, including …

Small structural differences govern the carbonic anhydrase II inhibition activity of cytotoxic triterpene acetazolamide conjugates

TC Denner, N Heise, J Zacharias, O Kraft, S Hoenke… - Molecules, 2023 - mdpi.com
Acetylated triterpenoids betulin, oleanolic acid, ursolic acid, and glycyrrhetinic acid were
converted into their succinyl-spacered acetazolamide conjugates. These conjugates were …

Synthesis, antimicrobial evaluation and docking studies of oxazolone-1, 2, 3-triazole-amide hybrids

L Kumar, K Lal, A Kumar, A Kumar - Research on Chemical Intermediates, 2021 - Springer
In an attempt to develop quality antimicrobial agents, a series of oxazolone-1, 2, 3-triazole-
amide hybrids were obtained from oxazolone tethered with a terminal alkyne and in situ …

Design, synthesis, in-vitro biological profiling and molecular docking of some novel oxazolones and imidazolones exhibiting good inhibitory potential against …

I Saleem Naz Babari, M Islam, H Saeed… - Journal of …, 2024 - Taylor & Francis
Heterocyclic compounds with oxazole and imidazole rings in their structure have disclosed
momentous biological aptitudes. Taking into account their superlative attributes, the present …

Structure based exploration of mitochondrial alpha carbonic anhydrase inhibitors as potential leads for anti-obesity drug development

I Padhy, T Sharma, B Banerjee, S Mohapatra… - DARU Journal of …, 2024 - Springer
Background Obesity has emerged as a major health challenge globally in the last two
decades. Dysregulated fatty acid metabolism and de novo lipogenesis are prime causes for …

Discovery of natural compounds as potential inhibitors of human carbonic anhydrase II: An integrated virtual screening, docking, and molecular dynamics simulation …

F Anjum, F Ali, T Mohammad, A Shafie… - OMICS: A Journal of …, 2021 - liebertpub.com
Carbonic anhydrase II (CAII) is one of the zinc metalloenzymes that catalyze the reversible
hydration of carbon dioxide, leading to the formation of bicarbonate and proton. CAII plays a …

Structure-guided design and development of vanillin-triazole conjugates as potential MARK4 inhibitors targeting hepatocellular carcinoma

S Ahmed, P Khan, I Irfan, S Anwar, A Shamsi… - Journal of Molecular …, 2023 - Elsevier
Microtubule affinity-regulating kinase 4 (MARK4) is a potential therapeutic target for cancer
therapy, as it plays a crucial role in cell division and metastasis. Vanillin is an essential …

Vanillin-Isatin Hybrid-Induced MARK4 Inhibition As a Promising Therapeutic Strategy against Hepatocellular Carcinoma

S Ahmed, A Queen, I Irfan, MN Siddiqui… - ACS …, 2024 - ACS Publications
Microtubule affinity-regulating kinase 4 (MARK4) is a serine-threonine kinase that
phosphorylates microtubule-associated proteins (MAPs) and increases the microtubule …