Results 261 to 270 of about 30,998 (353)

A Bioinspired Approach to Mechanically Reinforce Collagen‐Rich Tissues Using Modularly Defined Stilbenoids

open access: yesBiopolymers, Volume 117, Issue 1, January 2026.
A schematic diagram of dentin biomodification using modularly defined stilbenoids (MoDS). Stilbenoids interact with type I collagen at multiple hierarchical levels, inducing intermolecular and inter‐microfibrillar cross‐linking that enhances dentin viscoelastic properties, structural stability, and biocompatibility.
Mahmoud Sayed Ahmed   +4 more
wiley   +1 more source

The State of Knowledge of the Primary and Secondary Metabolites of the Iris Genus

open access: yesChemistry &Biodiversity, Volume 23, Issue 1, January 2026.
The genus Iris L. (Iridaceae) comprises over 320 species, primarily found in the northern hemisphere. Iris species are important in horticulture, folklore and medicine, and contain a variety of primary and secondary metabolites with significant biological activity.
Olha Mykhailenko   +3 more
wiley   +1 more source

Sulphur Analogues of Homoisoflavonoids as Potential Treatments for Neovascular Eye Diseases

open access: yesChemMedChem, Volume 21, Issue 2, January 2026.
Neovascular eye diseases are characterised by the abnormal growth of often fragile blood vessels in the eye. Treatment focuses on reducing angiogenesis as well as reducing oxidative stress induced inflammation, a key underlying cause. Synthetic sulphur analogues of naturally occurring homoisoflavonoids, synthesised in three steps, have shown promise as
Jacob D. Hiles   +9 more
wiley   +1 more source

The complete mitochondrial genome of Bauhinia variegata (Leguminosae). [PDF]

open access: yesMitochondrial DNA B Resour
Sun C   +10 more
europepmc   +1 more source

A Scalable and Sustainable Synthesis of Indirubin Frameworks Enabled by Deep Eutectic Solvents

open access: yesChemSusChem, Volume 19, Issue 1, January 2026.
A sustainable protocol for the synthesis of indirubin in a choline chloride/urea deep eutectic solvent at 70°C under air affords the product in 70% yield without chromatography. The method is robust, scalable to pilot scale, and enables late‐stage functionalization, granting access to a wide range of indirubin derivatives. CHEM21 green metrics validate
Biagio Delvecchio   +5 more
wiley   +1 more source

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