Results 21 to 30 of about 6,787 (215)

5,8-Dihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one (brasixanthone B)

open access: yesIUCrData, 2023
The title compound (trivial name brasixanthone B), C23H22O5, isolated from Calophyllum gracilentum, is characterized by a xanthone skeleton of three fused six-membered rings plus an additional fused pyrano ring and one 3-methylbut-2-enyl side chain.
Nurr Maria Ulfa Binti Seruji   +6 more
doaj   +1 more source

Xanthones with Antiproliferative Effects on Prostate Cancer Cells from the Stem Bark of

open access: yesNatural Product Communications, 2012
Investigations of the constituents of the stem barks of Garcinia xanthochymus have yielded two new compounds, garcinenones X (1) and Y (2), along with five known xanthones, 1,4,5,6-tetrahydroxy-7-(3-methylbut-2-enyl)xanthone (3), 1,4,6-trihydroxy-5 ...
Feng Ji   +6 more
doaj   +1 more source

Cytotoxic Xanthones from the Leaves of

open access: yesNatural Product Communications, 2007
Two new xanthones, 7-hydroxydesoxymorellin ( 1 ) and isocaledonixanthone D ( 2 ), and four known ones, gaudichaudione H, 1,7-dihydroxy-3-methoxy-2-(3-methyl-2-butenyl)xanthone, 1,5-dihydroxy-3-methoxy-2-(3-methyl-2-butenyl)xanthone, and 1,3,7-trihydroxy ...
Rozida Mohd Khalid   +5 more
doaj   +1 more source

Chemical Constituents From the Bark of

open access: yesNatural Product Communications, 2020
The phytochemical investigation of the methanol extract of bark of Garcinia oblongifolia yielded a new xanthone derivative 1,3,8-trihydroxy-6’,6’-dimethylpyrano (2’,3’:5,6) xanthone ( 5 ) along with 8 known compounds, including 1,2,5-trihydroxy-6 ...
Yutong Han   +5 more
doaj   +1 more source

Quantitative structure–activity relationship (QSAR) and molecular docking of xanthone derivatives as anti-tuberculosis agents

open access: yesJournal of Clinical Tuberculosis and Other Mycobacterial Diseases, 2020
Quantitative structure–activity relationship (QSAR) and molecular docking approach were carried out to design novel anti-tuberculosis agents based on xanthone derivatives.
Emmy Yuanita   +4 more
doaj   +1 more source

Synthesis, Biological Evaluation, and In Silico Studies of Novel Aminated Xanthones as Potential p53-Activating Agents

open access: yesMolecules, 2019
Xanthone scaffold has been regarded as an attractive chemical tool in the search for bioactive molecules with antitumor activity, and in particular two xanthone derivatives, 12-hydroxy-2,2-dimethyl-3,4-dihydro-2H,6H-pyrano [3,2-b]xanthen-6-one (4) and 3 ...
Agostinho Lemos   +7 more
doaj   +1 more source

Characterization of Antioxidant and α-Glucosidase Inhibitory Compounds of Cratoxylum formosum ssp. pruniflorum and Optimization of Extraction Condition

open access: yesAntioxidants, 2023
Cratoxylum formosum ssp. pruniflorum (Kurz.) Gogel (Guttiferae), called kuding tea, is widely distributed in Southeast Asia. In this study, the constituents and biological activity of C. formosum ssp. pruniflorum were investigated. Extract of its leaves,
Heewon An   +10 more
doaj   +1 more source

Chemometrically Assisted Optimization of Pregabalin Fluorescent Derivatization Reaction with a Novel Xanthone Analogue and Validation of the Method for the Determination of Pregabalin in Bulk via a Plate Reader

open access: yesMolecules, 2022
Quantitation of chromophore-free analytes is always a challenge. To this purpose, derivatization of the analyte constitutes a common strategy, leading to a product with a strong signal. In the current study, a novel xanthone analogue was utilized for the
Nikolaos Kritikos   +6 more
doaj   +1 more source

Antiprotozoal and Antibacterial Activity of Ravenelin, a Xanthone Isolated from the Endophytic Fungus Exserohilum rostratum

open access: yesMolecules, 2021
The natural compound ravenelin was isolated from the biomass extracts of Exserohilum rostratum fungus, and its antimicrobial, antiplasmodial, and trypanocidal activities were evaluated.
Jeferson Rodrigo Souza Pina   +12 more
doaj   +1 more source

Donor–Acceptor Pentacene Analogues With Near‐Infrared Emission and Tunable Aromaticity

open access: yesAngewandte Chemie, Volume 138, Issue 20, 11 May 2026.
Air‐ and photostable heterocyclic pentacene analogues with donor and acceptor groups flanking a para‐quinodimethane core exhibit large dipole moments, narrow bandgaps, reversible redox behavior, and NIR‐I to NIR‐II absorption and emission with pronounced solvatochromism.
Krzysztof Nowak   +6 more
wiley   +2 more sources

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