Despite the advancements in the development of anticancer agents, more effective and
safer anticancer drugs still need to be developed as the current agents cause unwanted side …

New conjugates of substituted 1, 2, 3-triazoles linked to 1, 2, 4-triazoles were synthesized
starting from the appropriate S-propargylated 1, 2, 4-triazoles 7 and 8. Ligation of 1, 2, 4 …

SBFI26, an inhibitor of FABP5, has been shown to suppress the proliferation and metastasis
of tumour cells. However, the underlying mechanism by which SBFI26 induces ferroptosis in …

Quinoline‐based thiazolidinone heterocycles exhibited potent activity in the field of cancer
therapy. Hence, ten quinoline‐based thiazolidinone derivatives were evaluated for their …

Apoptosis is often called programmed cell death and is defined as a self-directed cell
destruction process. It is different from necrosis due to the activation of caspases during this …

Twelve 7‐chloroquinoline derivatives were designed and synthesized using the principle of
molecular hybridization through the coupling of 2‐[2‐(7‐chloroquinolin‐4‐ylthio)‐4 …

Abstract A novel series of 4-(1, 2, 3-triazol-1-yl) salicylic acid derivatives was synthesized
from 4-azidosalicylic acid and diverse alkynes using copper catalyzed azide-alkyne …

The synthesis, structural analysis, and evaluation of the photophysical properties of twelve
novel 2‐aryl (heteroaryl)‐6‐(4‐alkyl (aryl)‐1H‐1, 2, 3‐triazol‐1‐yl)‐4‐(trifluoromethyl) …

Abstract A series of 1, 2, 3‐triazole derivatives based on the quinoline–benzimidazole hybrid
scaffold was designed, synthesized, and screened against a panel of NCI‐60 humanoid …

We described here a simple and metal‐free protocol to synthesize [1, 2, 3] triazolo [1, 5‐a]
quinoline 3‐carboxamides through a two‐step synthetic strategy, in which the first step uses …