Neuroprotective Mechanisms of <i>Red Algae</i>-Derived Bioactive Compounds in Alzheimer's Disease: An Overview of Novel Insights. [PDF]
Wang T, Shi W, Mao Z, Xie W, Wan G.
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Unveiling the Anti-Aging Potential of Marine Natural Bioproducts. [PDF]
Rosic N.
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Expression of Fluorescence Reporters and Natural Products in Native Gut <i>Escherichia coli</i>. [PDF]
Liu D +4 more
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Commercial importance of seaweeds: an overview. [PDF]
Rath S +5 more
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Sustainable Extraction of Prospective Cosmetic Ingredients from Colombian Marine Macroalgae Using Natural Deep Eutectic Solvents. [PDF]
Tamayo-Rincón VM +8 more
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Comprehensive Extraction and Biological Activities of Mycosporine-like Amino Acids and Glyceroglycolipids Extracts from Two Macroalgae Ecklonia kurome and Ulva lactuca. [PDF]
Wei X +10 more
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Researches on the stability of porphyra-334 solution and its influence factors
Journal of Ocean University of China, 2004The stability of porphyra-334 in solutions of different pH values at different temperatures was studied. In high acidic conditions, below pH3, the absorption maximum, λmax, of porphyra-334 shows hypsochromic shift towards lower wavelength and the absorbance also has a light decrease.
Shingo Matsukawa +2 more
exaly +2 more sources
Intrinsic Nature of the Ultrafast Deexcitation Pathway of Mycosporine-like Amino Acid Porphyra-334
The Journal of Physical Chemistry A, 2022Porphyra-334 is a member of natural UV-screening compounds named mycosporine-like amino acids found in several marine organisms. The UV excited porphyra-334 has been identified to deexcite quickly by puckering the intramolecular cyclohexenimine ring; however, the reason for such a ring-puckering occurrence is yet unclear.
Makoto Hatakeyama, Shinichiro Nakamura
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Antioxidative activities of a mycosporine-like amino acid, porphyra-334
Fisheries Science, 2008Antioxidative activities of porphyra-334, a mycosporine-like amino acid extracted from laver were evaluated. Oxidation of linoleic acid induced by an alkyl-radical 2,2′-azobis (2-amidinopropane) dihydrochloride (AAPH) was successfully suppressed by porphyra-334 (0–200 μM).
Tatsuya Sugawara +2 more
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