Organotin(IV) derivatives of amide-based carboxylates: Synthesis, spectroscopic characterization, single crystal studies and antimicrobial, antioxidant, cytotoxic, anti-leishmanial, hemolytic, noncancerous, anticancer activities

Ti3C2 nanosheets with broad-spectrum antioxidant activity for cytoprotection against oxidative stress

“…Compared the DPPH˙ scavenging ability with other antioxidants or nanoparticles (Table S2†), Ti 3 C 2 can remove DPPH˙ in a smaller dose and shorter time, which indicates that Ti 3 C 2 has strong free radical scavenging ability and fast response. 48–51…”

“…Compared the DPPHc scavenging ability with other antioxidants or nanoparticles (Table S2 †), Ti 3 C 2 can remove DPPHc in a smaller dose and shorter time, which indicates that Ti 3 C 2 has strong free radical scavenging ability and fast response. [48][49][50][51] Considering ROS play the critical role in regulation of oxidative stress balance, three representative ROS in biological conditions, H 2 O 2 , cOH and O À$ 2 , were selected to investigate systematically the powerful ROS scavenging capabilities of Ti 3 C 2 . The ability of Ti 3 C 2 to reduce H 2 O 2 is evaluated by using HRP-H 2 O 2 -TMB system, which is a classic enzymatic reaction.…”

Two novel macrocyclic organotin (IV) carboxylates based on bipyrazoledicarboxylic acid derivatives: Syntheses, crystal structures and antifungal activities

“…8,9 In fact, the literature reports that organotin carboxylates can act as antitumor, 8,9 antiviral, 10,11 antifungal, 12,13 antibacterial, 14,15 anti-proliferative, 16,17 anti-inflammatory, 18 and antioxidant potent agents. 19,20 Among the studies reporting on the various types of organotin complexes, only a few describe the synthesis and characterization of macrocyclic organotin compounds.…”

Anthracene appended organotin (IV) compounds: Synthesis, structure elucidation and their cytotoxicity against A549 and RBL cancer cell lines

“…Among these compounds, triorganotin (IV) carboxylates (R 3 SnOOCR′) exhibit a wide range of structural variations, with the co‐ligands playing a pivotal role 17,18 . The biological activity of R 3 SnOOCR′ is strongly influenced by the coordinated R groups and carboxylate ligand 19–21 …”