Results 51 to 60 of about 664 (168)
, 2020 Supplemental material, Supplementary_Information for Synthesis, cytotoxicity evaluation, and molecular modeling studies of 2,N10-substituted acridones as DNA-intercalating agents by Nisachon Khunnawutmanotham, Watthanachai Jumpathong, Chatchakorn ...
Supanna Techasakul (8461797) +4 more
core +1 more source
, 2016 The reaction of silylaryl triflates, CsF, and ortho-heteroatom-substituted benzoates affords a general and efficient way to prepare biologically interesting xanthones, thioxanthones, and acridones.
Jian Zhao (219525) +1 more
core +1 more source
, 2016 Insertion of benzene rings into the amide bond using the reactive intermediate benzyne is described. Aromatic amides undergo smooth insertion when treated with O-triflatophenyl silane benzyne precursors, producing versatile aminobenzophenone products in ...
Didier G. Pintori (2151043) +1 more
core +2 more sources
Alkylation of Acridone and Thioacridone
, 1987 Department of Chemistry, University of Kalyani, Kalyani-741 235 Manuscript received 8 October 1986, accepted 22 April 1987 Alkylation of Acridone and Thioacridone.
S. K. CHATTOPADHYA +2 more
openaire +1 more source
Boron Neutron Capture Therapy at a Crossroads: Translational Gap and Emerging Delivery Agents
Chemistry – A European Journal, Volume 32, Issue 17, 5 May 2026.This review surveys recent advances in boron delivery agents for BNCT, emphasizing the shift from classical small molecules to multifunctional nanocarriers and theranostic systems. By integrating targeting, imaging, and therapy, next‐generation boron compounds aim to bridge the gap between (bio)chemical innovation and clinical translation.
Christoph Selg, Evamarie Hey‐Hawkins
wiley +1 more source
Acridone alkaloids. X. 13C-Nuclear magnetic resonance spectra of acridone alkaloids.
Chemical and Pharmaceutical Bulletin, 1983 The 13C-nuclear magnetic resonance spectra of twenty-seven acridone alkaloids including angular pyrano [2, 3-c] acridones and linear pyrano [3, 2-b] acridones have been analyzed and assigned. The information should be useful for the structure elucidation of new acridone alkaloids.
FURUKAWA, HIROSHI +2 more
openaire +2 more sources
The FEBS Journal, Volume 293, Issue 9, Page 2673-2691, May 2026.Quinolones are valuable scaffolds for drug discovery but are rare in nature. Here, we show that two fungal enzymes, AthePKS and FerePKS, can generate 2‐quinolones and two additional heteroaromatic scaffolds. Using AthePKS, we designed an artificial enzymatic cascade towards an antimicrobial quinolone from a simple precursor and implemented it in E ...
Nika Sokolova +5 more
wiley +1 more source
Aggregate, Volume 7, Issue 4, April 2026.In a series of indolo[3,2‐b]carbazoles (X‐ICZ‐p1; X = F, Cl, Br), the afterglow properties are shaped by modulating intersystem crossing (ISC/rISC) and phosphorescence rates. F/Cl‐ICZ‐p1 systems show moderate rates, achieving color‐tunable, dual‐mode afterglow in polymethyl methacrylate from persistent thermally activated delayed fluorescence (pTADF ...
Jiang Zhao +4 more
wiley +1 more source
Crop Protection and Treatment: Studying Fungal Membrane Damage by Tetrahydroacridine Derivatives
Biomedical and Biotechnology Research JournalBackground: The widespread use of antibiotics has led to the emergence of drug-resistant strains, posing a significant challenge to global public health. Inspired by natural products, this study synthesized three series of tetrahydroacridine derivatives.
Yanhui Zhao +5 more
doaj +1 more source
Angewandte Chemie, Volume 138, Issue 11, 9 March 2026.A metallosupramolecular receptor binds squaraine dyes with high affinity and enables efficient dark resonance energy transfer (DRET) that generates bright near‐infrared emission with large pseudo‐Stokes shifts. ABSTRACT A metal‐organic cage was obtained by combining acridone‐based dipyridyl ligands with Pd2+ ions. The cage acts as a potent receptor for
Damien W. Chen +5 more
wiley +1 more source