Results 91 to 100 of about 4,197 (216)

Bioactive Phytochemical Compounds in Medicago sativa L. (Alfalfa): A Systematic Review of Biological Properties and Therapeutic Relevance in Nutraceutical and Functional Food Implications

open access: yesFood Frontiers, Volume 7, Issue 2, March 2026.
ABSTRACT Medicago sativa L. (alfalfa) harbors a remarkably diverse reservoir of bioactive secondary metabolites. Flavonoids, isoflavones, and triterpenoid saponins dominate its bioactivity landscape, driving potent antioxidant, anti‐inflammatory, antimicrobial, estrogenic, hypolipidemic, and cytotoxic actions through redox modulation, membrane ...
Parham Joolaei Ahranjani   +3 more
wiley   +1 more source

Medium-Sized Carbocycles and Ethers from 4-Pyrones:  A Photocyclization− Fragmentation Approach1 [PDF]

open access: yes, 2016
Medium-Sized Carbocycles and Ethers from 4-Pyrones:  A Photocyclization− Fragmentation ...
Mark L. Pugh (1617016)   +3 more
core   +1 more source

Reactivity of Carbonyl Group in y-Pyrones and in y-Pyridones. [PDF]

open access: yes, 1935
Reactivity of Carbonyl Group in \(\gamma\)-Pyrones and in \(\gamma ...
S. S DESHAPANDE   +2 more
core   +1 more source

Activation of the Nuclear Factor E2-Related Factor 2 Pathway by Novel Natural Products Halomadurones A–D and a Synthetic Analogue

open access: yesMarine Drugs, 2013
Two novel chlorinated pyrones, halomadurones A and B, and two novel brominated analogues, halomadurones C and D, were isolated from a marine Actinomadura sp. cultivated from the ascidian Ecteinascidia turbinata.
Thomas P. Wyche   +6 more
doaj   +1 more source

Alkynyl triazenes enable divergent syntheses of 2-pyrones [PDF]

open access: yes
The 2-pyrone motif occurs frequently in bioactive natural products and is appreciated as synthetic intermediates. However, only few methods allow for diversifying functional group modifications on this relevant heterocycle.
Bormann, Carl Thomas   +3 more
core   +1 more source

Evaluation of α-Pyrones and Pyrimidones as Photoaffinity Probes for Affinity-Based Protein Profiling [PDF]

open access: yes, 2016
α-Pyrones and pyrimidones are common structural motifs in natural products and bioactive compounds. They also display photochemistry that generates high-energy intermediates that may be capable of protein reactivity.
Oliver A. Battenberg (2178426)   +2 more
core   +1 more source

α‑Pyrones with Diverse Hydroxy Substitutions from Three Marine-Derived Nocardiopsis Strains [PDF]

open access: yes, 2016
Eight new α-pyrones 1–8 and three known α-pyrones 9–11 were isolated from three marine-derived Nocardiopsis strains SCSIO 10419, SCSIO 04583, and SCSIO KS107. The structures of compounds 1–8 were elucidated by comprehensive spectral analyses.
Wenjun Zhang (685002)   +9 more
core   +1 more source

Syntheses of α-Pyrones Using Gold-Catalyzed Coupling Reactions [PDF]

open access: yes, 2015
Sequential alkyne activation of terminal alkynes and propiolic acids by gold(I) catalysts yields compounds having α-pyrone skeletons. Novel cascade reactions involving propiolic acids are reported that give rise to α-pyrones with different substitution ...
Mingji Dai (1265700)   +3 more
core   +1 more source

Identification and isolation of insecticidal oxazoles from Pseudomonas spp.

open access: yesBeilstein Journal of Organic Chemistry, 2012
Two new and five known oxazoles were identified from two different Pseudomonas strains in addition to the known pyrones pseudopyronine A and B. Labeling experiments confirmed their structures and gave initial evidence for a novel biosynthesis pathway of ...
Florian Grundmann   +7 more
doaj   +1 more source

Pyran Rings Containing Polyketides from Penicillium raistrickii

open access: yesMarine Drugs, 2016
Five new pyran rings containing polyketides, penicipyrans A–E (1–5), together with the known pestapyrone A (6), were isolated from the saline soil-derived Penicillium raistrickii. Their structures were determined by interpretation of NMR and HRESIMS data.
Li-Ying Ma   +6 more
doaj   +1 more source

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