Results 131 to 140 of about 38,750 (255)
Radical Sampling Enabled Saturated N-Heterocycle Cyclization. [PDF]
Cai Q +6 more
europepmc +1 more source
A benzo‐21‐crown‐7 BODIPY dye (fluorescent probe) serves as a highly selective fluorescent probe for Ba2+ in aqueous solution. Ba2+ binding triggers a strong fluorescence enhancement, enabling sensitive detection with high selectivity, pH stability, and robustness under prolonged illumination.
Thomas Schwarze +3 more
wiley +1 more source
Switchable annulation paths to diverse N-bridged bicyclic scaffolds via ligand-directed dicarbonylation. [PDF]
Liu YK, Yang P, Wang LC, Bao ZP, Wu XF.
europepmc +1 more source
1,2‐Disubstituted ferrocene analogues bearing hydantoin or rhodanine synthons were synthesised and assessed for antitrypanosomatid activity. An antileishmanial early lead, analogue 23, acting through ROS generation and hence oxidative stress, was uncovered.
Maryna Saayman +7 more
wiley +1 more source
Discovery of Novel Piperidinyl-Based Benzoxazole Derivatives as Anticancer Agents Targeting VEGFR-2 and c-Met Kinases. [PDF]
Eldehna WM +11 more
europepmc +1 more source
Target‐induced disulfide ligation of PNA twin probes promotes pyrene excimer formation for nucleic acid detection. ABSTRACT The development of methods for detecting specific nucleic acids is important for early diagnosis and treatment of diseases at the genetic level.
Yutaka Ouchi +9 more
wiley +1 more source
Development of Glycoconjugated MAGL Inhibitors with Glucose-Dependent Antiproliferative Activity. [PDF]
Bononi G +10 more
europepmc +1 more source
Investigation of four medicinal plants of the family Myrtaceae. ABSTRACT Compounds derived from natural sources continue to serve as chemical scaffolds for designing prophylactic/therapeutic options for human healthcare. This study aimed to evaluate the phytochemical composition, antioxidant potential, in vitro anti‐inflammatory, antibacterial and ...
Archana Joshi +8 more
wiley +1 more source
Identification of quinolinyl-containing dual soluble epoxide hydrolase/fatty acid amide hydrolase inhibitors with moderate potency towards acetylcholinesterase. [PDF]
Gonzalez M +5 more
europepmc +1 more source

