Literatura científica selecionada sobre o tema "Bio-Sourced molecules"
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Artigos de revistas sobre o assunto "Bio-Sourced molecules"
Marchand, Guillaume, Gabin Fabre, Nidia Maldonado-Carmona, Nicolas Villandier e Stéphanie Leroy-Lhez. "Acetylated lignin nanoparticles as a possible vehicle for photosensitizing molecules". Nanoscale Advances 2, n.º 12 (2020): 5648–58. http://dx.doi.org/10.1039/d0na00615g.
Texto completo da fonteMalucelli, Giulio. "Bio-Sourced Flame Retardants for Textiles: Where We Are and Where We Are Going". Molecules 29, n.º 13 (27 de junho de 2024): 3067. http://dx.doi.org/10.3390/molecules29133067.
Texto completo da fonteVillamil Watson, Daniel A., e David A. Schiraldi. "Biomolecules as Flame Retardant Additives for Polymers: A Review". Polymers 12, n.º 4 (7 de abril de 2020): 849. http://dx.doi.org/10.3390/polym12040849.
Texto completo da fontePolat, M. Fatih. "Synthesis of Asebogenin and Balsacone A Precursor by a Novel Synthetic Strategy: Recent Opportunities for and Challenges of Total Synthesis of Balsacone A". Molecules 27, n.º 11 (30 de maio de 2022): 3523. http://dx.doi.org/10.3390/molecules27113523.
Texto completo da fonteCuria, S., A. F. Barclay, S. Torron, M. Johansson e S. M. Howdle. "Green process for green materials: viable low-temperature lipase-catalysed synthesis of renewable telechelics in supercritical CO 2". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 373, n.º 2057 (28 de dezembro de 2015): 20150073. http://dx.doi.org/10.1098/rsta.2015.0073.
Texto completo da fonteLambert, Prescilla, Mahado Said-Ahmed, Charafeddine Jama e Mounim Lebrini. "Molecules from Sargassum algae as Green Inhibitor for C38 in HCl Medium: Extraction, Characterization and Electrochemical Study". Coatings 13, n.º 12 (13 de dezembro de 2023): 2076. http://dx.doi.org/10.3390/coatings13122076.
Texto completo da fonteShahaji Jawale, Sushil. "BIOCHEMICAL STUDY OF FRESHWATER FISH CLARIAS BATRACHUS (L.) INFECTED WITH CESTODE PARASITE, LYTOCESTUS SP. FROM DISTRICT JALGAON, INDIA". International Journal of Biological Innovations 05, n.º 02 (2023): 49–53. http://dx.doi.org/10.46505/ijbi.2023.5207.
Texto completo da fonteLuscombe, Christine Keiko. "(Invited) Organic Dyes Derived from Molecules in Cacao Beans for Use in Lighting Applications". ECS Meeting Abstracts MA2022-01, n.º 20 (7 de julho de 2022): 1101. http://dx.doi.org/10.1149/ma2022-01201101mtgabs.
Texto completo da fonteSpalletta, Alexis, Nicolas Joly e Patrick Martin. "Optimization of Enzymatic Synthesis of D-Glucose-Based Surfactants Using Supported Aspergillus niger Lipase as Biocatalyst". Chemistry 5, n.º 3 (23 de agosto de 2023): 1855–69. http://dx.doi.org/10.3390/chemistry5030127.
Texto completo da fonteEhsani, Masoume, Denis Kalugin, Huu Doan, Ali Lohi e Amira Abdelrasoul. "Bio-Sourced and Biodegradable Membranes". Applied Sciences 12, n.º 24 (14 de dezembro de 2022): 12837. http://dx.doi.org/10.3390/app122412837.
Texto completo da fonteTeses / dissertações sobre o assunto "Bio-Sourced molecules"
Dascalu, Anca-Elena. "Bioantibio, biosourced antibacterial and antifungal molecules". Thesis, Lille, 2019. http://www.theses.fr/2019LILUS052.
Texto completo da fonteThe lack of therapeutic innovations has recently reached a critical level, considering antibiotic treatments. This issue, correlated with the appearance of multidrug-resistant bacteria underlined the need for new approaches towards the discovery of innovative antibiotics. As a consequence, the BIOANTIBIO project was proposed.The two main initially envisioned applications for the most active compounds being:• Additives for the formulation of innovative materials (eg paints and coatings) in order to guarantee their durability in storage (working in collaboration with IFMAS).• Drugs: antibacterial and antifungal agents, particularly for the development of antimicrobial agents against drug-resistant bacteria for human health protection.Employing natural molecules to develop novel antifungal or antimicrobial classes can be challenging. Nevertheless, nature is known to inspire chemists in the synthesis of molecules with improved biological properties and within this project we have demonstrated that even the well known pyroglutamic acid is still to be exploited as a scaffold
Rabaud, Dorian. "Synthesis and development of new bio-sourced Low Molecular Weight Organogelators". Electronic Thesis or Diss., Sorbonne université, 2022. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2022SORUS463.pdf.
Texto completo da fonteOrganogels are supramolecular gels or physical gels formed from organogelators in organic solvents. These organogelators or low molecular weight organogelators (LMOGs) are small organic molecules (< 2000 Da) capable of self-assembly. This leads to the formation of elongated structures, mainly fibers, which form an entangled self-assembled fibrillar network (SAFiN), whose assembly mechanism is driven by non-covalent interactions. The objective of this thesis is to develop new organogelators from biobased building blocks. In a first step, we synthesized molecules based on tannic acid. By varying the nature of the groups and the chain lengths, we adapted the solubility of the molecules and mapped a family of molecules that, however, did not show interesting properties. Subsequently, we synthesized FDCA-based molecules containing amide functions. By varying the nature of the amine and the chain lengths, we discovered a new family of organogelators
Ruggieri, Francesca. "Putting nature back into drug discovery : selection, design and synthesis of bioinspired chemical libraries for the discovery of new antibacterials". Electronic Thesis or Diss., Université de Lille (2022-....), 2024. http://www.theses.fr/2024ULILS013.
Texto completo da fonteNatural products (NPs) have declined in popularity since the introduction of synthetic small molecules several years ago. Many are the reasons behind this choice, such as difficulties in access and supply, complexities of NP chemistry and the advent of combinatorial chemistry. However, NPs offer many interesting properties compared to conventional synthetic molecules, which confer both advantages and challenges for the drug discovery process. Usually, NPs are characterized by a higher number of sp3 carbons and stereogenic centres, large scaffold diversity and structural complexity. With half of the drugs approved by the FDA since 1994 being NPs or hemisynthetic derivatives and the recent stagnation in new drug research and development, it is becoming more and more evident that NPs should be reintroduced in the drug discovery process as a source of inspiration.Therefore, many strategies are now emerging for the construction of nature-inspired chemical libraries, such as “top-down” and “bottom-up” strategies. In “bottom-up” approaches, complexity is created starting from simple building blocks. On the other hand, “top-down” approaches are assumed to make structural modifications to an already complex NP.Our presented work describes two different approaches to enrich the chemical library of our research unit with NP-derived compounds. A “top-down” semisynthetic strategy was planned to obtain derivatives of lactucin and 11β,13-dihydrolactucin, two sesquiterpene lactones extracted from chicory roots. Thirty-six ester derivatives were synthesized in three steps (classical synthesis), together with two amine derivative libraries (using parallel synthesis). All the compounds were then tested against Mycobacterium tuberculosis and some promising hits were found (MICGFP < 1.2 μM). On the other hand, a “bottom-up” strategy allowed the synthesis of two analogues of the known natural antibiotic hygromycin A. This approach started from simple commercially available building blocks and employed a dearomatization strategy in the synthetic process.Together, we explored a broader chemical space, increased the structural diversity of our chemical library and discovered new potential antibacterial hits. Moreover, this work paves the way for the discovery of new antibacterial targets
Capítulos de livros sobre o assunto "Bio-Sourced molecules"
Kerton, Francesca M. "Ocean Resources for the Production of Renewable Chemicals and Materials". In Chemical Processes for a Sustainable Future, 443–58. The Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/bk9781849739757-00443.
Texto completo da fonteKrishnan, Mahalakshmi, Livya Catherene Martin, Parimalanandhini Duraisamy, Sangeetha Ravi, Beulaja Manikandan, Janarthanan Sundaram e Ramar Manikandan. "An Overview of Natural Steroid Sources and their Therapeutic Profile". In Steroids and their Medicinal Potential, 39–58. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/789815049336123010004.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Bio-Sourced molecules"
Refaa, Zakariaa, Mhamed Boutaous, Shihe Xin e Patrick Bourgin. "Towards the Enhancement of the Crystallization Kinetics of a Bio-Sourced and Biodegradable Polymer PLA (Poly (Lactic Acid))". In ASME 2014 4th Joint US-European Fluids Engineering Division Summer Meeting collocated with the ASME 2014 12th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fedsm2014-21952.
Texto completo da fonteBoutaous, Mhamed, Zakariaa Refaa, Matthieu Zinet, Shihe Xin e Patrick Bourgin. "Analysis of the Process-Structure-Behavior Interaction in Bio-Sourced Polymers: Role of the Crystallization Kinetics". In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-39729.
Texto completo da fonteKinaci, Emre, John Chea, Kirti Yenkie e Kylie Howard. "Converting Birch Bark Extracts into Bio-based Thermosets". In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/wcih1760.
Texto completo da fonte