Literatura científica selecionada sobre o tema "Cyclocurcumin"
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Artigos de revistas sobre o assunto "Cyclocurcumin"
Losantos, Raúl, Jérémy Pecourneau, Maxime Mourer, Stéphane Parant, Andreea Pasc e Antonio Monari. "trans–cis Photoisomerization of a biomimetic cyclocurcumin analogue rationalized by molecular modelling". Physical Chemistry Chemical Physics 23, n.º 22 (2021): 12842–49. http://dx.doi.org/10.1039/d1cp01224j.
Texto completo da fonteGasbarri, Carla, e Guido Angelini. "Cyclocurcumin as Promising Bioactive Natural Compound: An Overview". Molecules 29, n.º 7 (24 de março de 2024): 1451. http://dx.doi.org/10.3390/molecules29071451.
Texto completo da fonteKesharwani, Rajesh K., Simran Kumari, Dev Bukhsh Singh e Sandeep Tripathi. "A Docking Simulation Study of Some Herbal Molecules Against Influenza A Virus by Targeting Neuraminidase". Current Traditional Medicine 6, n.º 2 (27 de fevereiro de 2020): 147–54. http://dx.doi.org/10.2174/2215083805666190808092031.
Texto completo da fonteAdhikary, Ramkrishna, Charles A. Barnes, Rachel L. Trampel, Samuel J. Wallace, Tak W. Kee e Jacob W. Petrich. "Photoinducedtrans-to-cisIsomerization of Cyclocurcumin". Journal of Physical Chemistry B 115, n.º 36 (15 de setembro de 2011): 10707–14. http://dx.doi.org/10.1021/jp200080s.
Texto completo da fonteLi, Yunkui, Marirosa Toscano, Gloria Mazzone e Nino Russo. "Antioxidant properties and free radical scavenging mechanisms of cyclocurcumin". New Journal of Chemistry 42, n.º 15 (2018): 12698–705. http://dx.doi.org/10.1039/c8nj01819g.
Texto completo da fonteKim, Keunyoung, Jung-Jun Kim, Yeryeon Jung, Ji-Yoon Noh, Ahmed Shah Syed, Chul Young Kim, Moo-Yeol Lee, Kyung-Min Lim, Ok-Nam Bae e Jin-Ho Chung. "Cyclocurcumin, an Antivasoconstrictive Constituent ofCurcuma longa(Turmeric)". Journal of Natural Products 80, n.º 1 (9 de janeiro de 2017): 196–200. http://dx.doi.org/10.1021/acs.jnatprod.6b00331.
Texto completo da fonteMarazzi, Marco, Antonio Francés-Monerris, Maxime Mourer, Andreea Pasc e Antonio Monari. "Trans-to-cis photoisomerization of cyclocurcumin in different environments rationalized by computational photochemistry". Physical Chemistry Chemical Physics 22, n.º 8 (2020): 4749–57. http://dx.doi.org/10.1039/c9cp06565b.
Texto completo da fonteNgo, Thien, Keunyoung Kim, Yiying Bian, Gwang-Jin An, Ok-Nam Bae, Kyung-Min Lim e Jin-Ho Chung. "Cyclocurcumin from Curcuma longa selectively inhibits shear stress-induced platelet aggregation". Journal of Functional Foods 61 (outubro de 2019): 103462. http://dx.doi.org/10.1016/j.jff.2019.103462.
Texto completo da fontePecourneau, Jérémy, Raúl Losantos, Antonio Monari, Stéphane Parant, Andreea Pasc e Maxime Mourer. "Synthesis and Photoswitching Properties of Bioinspired Dissymmetric γ-Pyrone, an Analogue of Cyclocurcumin". Journal of Organic Chemistry 86, n.º 12 (8 de junho de 2021): 8112–26. http://dx.doi.org/10.1021/acs.joc.1c00598.
Texto completo da fonteLosantos, Raúl, Giacomo Prampolini e Antonio Monari. "A Portrait of the Chromophore as a Young System—Quantum-Derived Force Field Unraveling Solvent Reorganization upon Optical Excitation of Cyclocurcumin Derivatives". Molecules 29, n.º 8 (12 de abril de 2024): 1752. http://dx.doi.org/10.3390/molecules29081752.
Texto completo da fonteTeses / dissertações sobre o assunto "Cyclocurcumin"
Pecourneau, Jérémy. "Réponses photoinduites d'analogue biomimétique de la cyclocurcumine : vers des thérapies assistées par la lumière". Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0205.
Texto completo da fonteBeyond photodynamic therapy (PDT), there are several light-assisted therapeutic alternatives, including photothermal therapy (PTT) and photoisomerization, whose mechanical action would induce cellular damage within the membranes. Also, molecules able to simultaneously absorb two photons would overcome the need for high energy excitation per photon while maintaining sufficient tissue penetration. In this context, we were interested in designing and studying biomimetic analogues of cyclocurcumin (CC), a natural E/Z photoswitch. Guided by molecular modeling, those novel donor-acceptor compounds were structurally designed to increase the effective two-photon absorption cross section (σ2).First, we synthesized two classes of CC analogues bearing acceptor (oxo and malonitrile) and donor (hydroxy, alkoxy and amine) groups as well as a PEG arm to increase their hydrophilicity. Free in solution, the oxo derivatives show a reversible photoinduced isomerization, without any thermal isomerization in the dark, whereas the malonitrile derivatives do not photoswitch but undergo a vibrational relaxation. This is leading to a temperature increase, of interest in photothermal therapy. Finally, confined in a lipidic environment (liposomes bilayers and Langmuir monolayers), the direct E→Z isomerization kinetics of oxo compounds is strongly slowed down and no Z→E back isomerization is observed. Those compounds also showed a certain efficiency to disrupt membrane fluidity, more or less pronounced depending on the form, Z or E, the length of the alkoxy chain or the presence of the PEG unit. The malonitrile derivatives exhibit a diminished photothermal effect in lipid bilayers after several irradiation cycles.Taken together, this study is a proof of concept for the potential of photoinduced responses of cyclocurcumin analogs for disruption of membrane fluidity towards potential use in vivo
Trabalhos de conferências sobre o assunto "Cyclocurcumin"
Hidayah, Rizka Nurul, Dewi Santosaningsih e Roihatul Muti’ah. "Bioinformatics study of curcumin, demethoxycurcumin, bisdemethoxycurcumin and cyclocurcumin compounds in Curcuma longa as an antiviral agent via nucleocapsid on SARS-CoV-2 inhibition". In INTERNATIONAL CONFERENCE ON ORGANIC AND APPLIED CHEMISTRY (ICOAC) 2022. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0197724.
Texto completo da fonte