2022
DOI: 10.1016/j.molstruc.2022.132364
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Synthesis of novel naphthalimide tethered 1,2,3-triazoles: In vitro biological evaluation and docking study of anti-inflammatory inhibitors

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Cited by 20 publications
(11 citation statements)
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“…Bengam et al [ 38 ] designed and synthesized novel naphthalimide-1,2,3-triazole tethered heterocycles and evaluated their in vitro anti-inflammatory properties. Among the compounds tested, 32 displayed inhibitions comparable to the reference compound (diclofenac sodium).…”
Section: Five-membered Heterocyclic Compoundsmentioning
confidence: 99%
See 1 more Smart Citation
“…Bengam et al [ 38 ] designed and synthesized novel naphthalimide-1,2,3-triazole tethered heterocycles and evaluated their in vitro anti-inflammatory properties. Among the compounds tested, 32 displayed inhibitions comparable to the reference compound (diclofenac sodium).…”
Section: Five-membered Heterocyclic Compoundsmentioning
confidence: 99%
“…Among the evaluated compounds, N-benzyl-6-((1-(2nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)quinazolin-4-amine 31 was shown to have the highest inhibitory activity with an IC 50 value of 0.23 µM (see Figure 7). Bengam et al [38] designed and synthesized novel naphthalimide-1,2,3-triazole tethered heterocycles and evaluated their in vitro anti-inflammatory properties. Among the compounds tested, 32 displayed inhibitions comparable to the reference compound (di-clofenac sodium).…”
Section: 23-triazolementioning
confidence: 99%
“…Experimental). Azide derivative 9 reacted with thioglycolic acid in dry benzene under refluxing to afford new 3-((1,3dioxoisoindolin-2-yl)methyl)thiazolidine-2,4-dione (15). In the same manner, 3-oxobenzo[d]isothiazol-2(3H)-yl 16 and 3-oxo-1,3-dihydro-2H-indazol-2-yl 17 derivatives had been obtained via reaction of azide 9 with thiosalicylic acid and anthranilic acid, respectively under the same conditions (Scheme 4).…”
Section: Figure 1: Mechanism Of Azide Formation From Hydrazidesmentioning
confidence: 99%
“…Furthermore, hybrid of thiadiazole-phthalimide and triazole-phthalimide moieties have afforded remarkable cytotoxic effects. [14][15][16] Heterocyclic compounds that have five and six membered ring are considered as a pivotal scaffold of targeted drugs in pharmaceutical and medicinal chemistry, this is a results of their resemblance with many biologically efficient compounds in our body. Also, they provide many medicinal and biological applications such as antimicrobial, anticonvulsant, antibacterial, anticancer, anti-inflammatory and antifungal effects.…”
Section: Introductionmentioning
confidence: 99%
“…[ 10 ] Some of pyrimidinamine compounds had been commercialized as pesticides, such as the fungicides Ethirimol and Bupirimate, the insecticide Dicyclanil, and the herbicide Nicosulfuron. Triazole is another nitrogen‐linked heterocycle, which also possessed excellent activity, such as fungicidal, [ 11–13 ] herbicidal, [ 14 ] antiinflammatory, [ 15 ] antimicrobial, [ 16 ] antiviral, [ 17 ] and antioxidant [ 18 ] activities. Fused heterocycles often exhibited two heterocycles' properties.…”
Section: Introductionmentioning
confidence: 99%