Results 151 to 160 of about 36,678 (260)
Pyrrolo[3,4‐b]pyridin‐5‐ones are assembled in one pot manner through an Ugi‐Zhu reaction coupled to a cascade sequence (aza Diels‐Alder/N‐acylation/decarboxylation/dehydration). Pyrrolo[3,4‐b]pyridin‐5‐ones are fluorescence probes for local viscosity, polarity, protic environments, and solid‐state emission.
Ivette Morales‐Salazar +9 more
wiley +1 more source
Design, synthesis and antifungal activity of pyrazole ester derivatives. [PDF]
Shen Y +4 more
europepmc +1 more source
Eight novel N‐phenylpyrazoline derivatives bearing chlorothiophene moieties were synthesized and evaluated for anticancer activity against T47D, MCF7, and WiDr cell lines. Compound 2g showed the strongest cytotoxicity against WiDr cells (IC50 = 19.63 µg/mL) with the highest selectivity index (665.88), highlighting its potential as a selective ...
Nikma Farismatur Riza +4 more
wiley +1 more source
Novel benzofuran-furan-pyrano[2,3-<i>c</i>]pyrazole hybrids as potential anticancer agents: design, synthesis, <i>in silico</i> profiling, and multi-mechanistic biological evaluation. [PDF]
Hutanu ED +5 more
europepmc +1 more source
Copper-catalyzed radical carbonylation platform for the synthesis of <i>N</i>-acyl azoles under 1 bar of CO. [PDF]
Dai M, Yang ML, Wu XF.
europepmc +1 more source
Sesquiterpene lactones emerge as structurally diverse anticancer scaffolds with multifaceted mechanisms of action. Their biosynthesis, chemical diversity, structure–activity relationships, semisynthetic diversification, and molecular targets are integrated to highlight therapeutic opportunities and challenges.
Kedar Nimba Chaudhari +3 more
wiley +1 more source
Design, Synthesis, and Biological Evaluation of Pyrazolyl Thioureas (PTUs) as SIRT1 and SIRT2 Inhibitors. [PDF]
Lusardi M +10 more
europepmc +1 more source
A rapid, green MW/US‐assisted route was developed for synthesizing coumarin/azacoumarin‐based fused heterocycles. It enables efficient construction of pyrano[2,3‐b]pyridines and pyrazolo[3,4‐d]pyrimidinones under mild conditions. FT‐IR, NMR, MS, and elemental analysis fully confirmed the structures of the new products.
Sultanah M. Alhunayhin +5 more
wiley +1 more source
Fluorogenic Sydnones for Bioorthogonal Labeling of DNA
Conjugates of sydnones with cyanine‐styryl dyes combine bioorthogonal reactivity with fluorogenicity. The reactivity with bicyclo[6.1.0]non‐4‐yne (BCN)‐modified DNA showed second‐order rate constants of up to k2 = 2,300 M−1s−1 and fluorescence turn‐on by one magnitude of order.
Kerstin Müller +1 more
wiley +1 more source
In this article, a series of zwitterionic scorpionate ligands based on the anionic tris‐(pyrazolyl)borate ligand scaffold is presented. These ligands are used to prepare bis‐chelates with divalent manganese ions. The resulting complexes are studied via magnetic, crystallographic, and electrochemical means to characterize the charge–transfer‐induced ...
Matthew C. Kessinger +5 more
wiley +1 more source

