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Multifunctional Cinnamic Acid Derivatives [PDF]

open access: yesMolecules, 2017
Our research to discover potential new multitarget agents led to the synthesis of 10 novel derivatives of cinnamic acids and propranolol, atenolol, 1-adamantanol, naphth-1-ol, and (benzylamino) ethan-1-ol.
Aikaterini Peperidou   +4 more
doaj   +3 more sources

Pharmacological Potential of Cinnamic Acid and Derivatives: A Comprehensive Review [PDF]

open access: yesPharmaceuticals
Cinnamic acid, an organic acid naturally occurring in plants of the Cinnamomum genus, has been highly valued for its medicinal properties in numerous ancient Chinese texts.
Yu Tian   +7 more
doaj   +2 more sources

Recent advances in synthetic approaches for bioactive cinnamic acid derivatives [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Cinnamic acid derivatives represent a significant class of biologically active compounds exhibiting a broad spectrum of activities, such as antifungal, antidengue, antimetastatic, antimicrobial, antibacterial, and anticancer properties. Their preparation
Betty A. Kustiana   +2 more
doaj   +2 more sources

Cinnamic Acid Derivatives as Potential Multifunctional Agents in Cosmetic Formulations Used for Supporting the Treatment of Selected Dermatoses [PDF]

open access: yesMolecules
Cinnamic acid and its natural derivatives were primarily used in cosmetics as fragrance materials as well as skin and hair conditioners. Nowadays, not only natural but also synthetic cinnamic acid derivatives are used as active ingredients of cosmetic ...
Małgorzata Kabat   +2 more
doaj   +2 more sources

Cinnamic acid alleviates hypertensive left ventricular hypertrophy by antagonizing the vasopressor activity and the pro-cardiac hypertrophic signaling of angiotensin II [PDF]

open access: yesFrontiers in Pharmacology
BackgroundHypertension is the most common cause of pathological left ventricular hypertrophy, a condition causally associated with debilitating heart failure and cardiovascular events in hypertensive patients.
Yimeng Cui   +11 more
doaj   +2 more sources

Density Functional Theory, Molecular Docking Study, and In Vitro Antioxidant Activity of Cinnamic Acid Isolated From Piper betle Leaves [PDF]

open access: yesBiochemistry Research International
Piper betle is an edible plant known for its potent antioxidant activity. Among its phenolic constituents, cinnamic acid has been identified as a key compound contributing to this bioactivity.
Sefren Geiner Tumilaar   +3 more
doaj   +2 more sources

Cinnamic acid abrogates bisphenol A-induced hepatotoxicity via suppression of pro-inflammatory cytokine and modulation of gene expressions of antioxidant enzymes in rats [PDF]

open access: yesToxicology Reports
Bisphenol A (BPA) is regularly used to produce plastic products. Its hepatotoxicity has been unveiled. The effects of cinnamic acid on BPA exposure have not been comprehensively studied, and the key mechanism of action is yet to be unraveled.
Anne Adebukola Adeyanju   +4 more
doaj   +2 more sources

Encapsulation of Cinnamic Acid on Plant-Based Proteins: Evaluation by HPLC, DSC and FTIR-ATR

open access: yesPlants, 2021
Plant-based protein matrices can be used for the formulation of delivery systems of cinnamic acid. Pumpkin, pea and almond protein matrices were used for the formulation of dried complexes.
Mirela Kopjar   +5 more
doaj   +1 more source

Geroprotective activity of trans-cinnamic acid isolated from the Baikal skullcap (Scutellaria baicalensis)

open access: yesТехника и технология пищевых производств, 2022
Trans-cinnamic acid is a phenolic compound with a wide range of bioactive properties, including antioxidant and antibacterial effects. It also has high potential in the food and cosmetic industries. We aimed to isolate trans-cinnamic acid from the Baikal
Anastasiya M. Fedorova   +5 more
doaj   +1 more source

2,3,4,5,6-Pentafluoro-trans-cinnamic acid [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2013
The title compound, C9H3F5O2, crystallizes as O-H⋯O hydrogen-bonded carb-oxy-lic acid dimers that, together with C-H⋯F inter-actions and O⋯F [2.8065 (13) and 2.9628 (13) Å] and F⋯F [2.6665 (11), 2.7049 (12) and 2.7314 (12) Å] contacts, form a sheet-like structure.
Angélica Navarrete   +2 more
openaire   +3 more sources

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