Literatura académica sobre el tema "Cyclocurcumin"
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Artículos de revistas sobre el tema "Cyclocurcumin"
Losantos, Raúl, Jérémy Pecourneau, Maxime Mourer, Stéphane Parant, Andreea Pasc y 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 completoGasbarri, Carla y Guido Angelini. "Cyclocurcumin as Promising Bioactive Natural Compound: An Overview". Molecules 29, n.º 7 (24 de marzo de 2024): 1451. http://dx.doi.org/10.3390/molecules29071451.
Texto completoKesharwani, Rajesh K., Simran Kumari, Dev Bukhsh Singh y 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 febrero de 2020): 147–54. http://dx.doi.org/10.2174/2215083805666190808092031.
Texto completoAdhikary, Ramkrishna, Charles A. Barnes, Rachel L. Trampel, Samuel J. Wallace, Tak W. Kee y Jacob W. Petrich. "Photoinducedtrans-to-cisIsomerization of Cyclocurcumin". Journal of Physical Chemistry B 115, n.º 36 (15 de septiembre de 2011): 10707–14. http://dx.doi.org/10.1021/jp200080s.
Texto completoLi, Yunkui, Marirosa Toscano, Gloria Mazzone y 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 completoKim, Keunyoung, Jung-Jun Kim, Yeryeon Jung, Ji-Yoon Noh, Ahmed Shah Syed, Chul Young Kim, Moo-Yeol Lee, Kyung-Min Lim, Ok-Nam Bae y Jin-Ho Chung. "Cyclocurcumin, an Antivasoconstrictive Constituent ofCurcuma longa(Turmeric)". Journal of Natural Products 80, n.º 1 (9 de enero de 2017): 196–200. http://dx.doi.org/10.1021/acs.jnatprod.6b00331.
Texto completoMarazzi, Marco, Antonio Francés-Monerris, Maxime Mourer, Andreea Pasc y 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 completoNgo, Thien, Keunyoung Kim, Yiying Bian, Gwang-Jin An, Ok-Nam Bae, Kyung-Min Lim y Jin-Ho Chung. "Cyclocurcumin from Curcuma longa selectively inhibits shear stress-induced platelet aggregation". Journal of Functional Foods 61 (octubre de 2019): 103462. http://dx.doi.org/10.1016/j.jff.2019.103462.
Texto completoPecourneau, Jérémy, Raúl Losantos, Antonio Monari, Stéphane Parant, Andreea Pasc y 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 junio de 2021): 8112–26. http://dx.doi.org/10.1021/acs.joc.1c00598.
Texto completoLosantos, Raúl, Giacomo Prampolini y 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 completoTesis sobre el tema "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 completoBeyond 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
Actas de conferencias sobre el tema "Cyclocurcumin"
Hidayah, Rizka Nurul, Dewi Santosaningsih y 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". En INTERNATIONAL CONFERENCE ON ORGANIC AND APPLIED CHEMISTRY (ICOAC) 2022. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0197724.
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