Targeting regulated cell death (RCD) with small-molecule compounds in triple-negative breast cancer: a revisited perspective from molecular mechanisms to targeted …

M Liao, R Qin, W Huang, HP Zhu, F Peng… - Journal of Hematology & …, 2022 - Springer
Triple-negative breast cancer (TNBC) is a subtype of human breast cancer with one of the
worst prognoses, with no targeted therapeutic strategies currently available. Regulated cell …

Spirooxindole: a versatile biologically active heterocyclic scaffold

SS Panda, AS Girgis, MN Aziz, MS Bekheit - Molecules, 2023 - mdpi.com
Spirooxindoles occupy an important place in heterocyclic chemistry. Many natural
spirooxindole-containing compounds have been identified as bio-promising agents …

Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances

P Dhokne, AP Sakla, N Shankaraiah - European journal of medicinal …, 2021 - Elsevier
Small-molecule kinase inhibitors are being continuously explored as new anticancer
therapeutics. Kinases are the phosphorylating enzymes which regulate numerous cellular …

Discovery of new carbonic anhydrase IX inhibitors as anticancer agents by toning the hydrophobic and hydrophilic rims of the active site to encounter the dual-tail …

HO Tawfik, A Petreni, CT Supuran… - European journal of …, 2022 - Elsevier
The hydrophobic and the hydrophilic rims in the active site of human carbonic anhydrase IX
(hCA IX) which as well contains a zinc ion as part of the catalytic core, were simultaneously …

Anticancer potential of spirocompounds in medicinal chemistry: A pentennial expedition

D Bora, A Kaushal, N Shankaraiah - European Journal of Medicinal …, 2021 - Elsevier
Spirocompounds constitute an important class of organic frameworks enveloping numerous
pharmacological activities, among them, the promising anticancer potential of …

Design, synthesis and mechanistic study of new benzenesulfonamide derivatives as anticancer and antimicrobial agents via carbonic anhydrase IX inhibition

MTM Nemr, AM AboulMagd, HM Hassan, AA Hamed… - RSC …, 2021 - pubs.rsc.org
Changes in gene expression cause uncontrolled cell proliferation and consequently tumor
hypoxia. The tumor cells shift their metabolism to anaerobic glycolysis with a significant …

Spirocyclic derivatives as antioxidants: A review

K Acosta-Quiroga, C Rojas-Pena, LS Nerio… - RSC …, 2021 - pubs.rsc.org
In recent years, spiro compounds have attracted significant interest in medicinal chemistry
due to their numerous biological activities attributed primarily to their versatility and structural …

Choline chloride-based DES as solvents/catalysts/chemical donors in pharmaceutical synthesis

R Amoroso, F Hollmann, C Maccallini - Molecules, 2021 - mdpi.com
DES are mixtures of two or more compounds, able to form liquids upon mixing, with lower
freezing points when compared to the individual constituents (eutectic mixtures). This …

Novel coumarin-6-sulfonamides as apoptotic anti-proliferative agents: synthesis, in vitro biological evaluation, and QSAR studies

A Sabt, OM Abdelhafez, RS El-Haggar… - Journal of enzyme …, 2018 - Taylor & Francis
Herein, we report the synthesis of different novel sets of coumarin-6-sulfonamide derivatives
bearing different functionalities (4a, b, 8a–d, 11a–d, 13a, b, and 15a–c), and in vitro …

Enhancement of the tail hydrophobic interactions within the carbonic anhydrase IX active site via structural extension: Design and synthesis of novel N-substituted …

WM Eldehna, MF Abo-Ashour, A Nocentini… - European journal of …, 2019 - Elsevier
Herein we report the design and synthesis of novel N-substituted isatins-SLC-0111 hybrids
(6a-f and 9a-l). A structural extension approach was adopted via N-alkylation and N …