Literatura académica sobre el tema "Justicidin C"
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Artículos de revistas sobre el tema "Justicidin C"
Luo, Jiaoyang, Yichen Hu, Jia'an Qin y Meihua Yang. "Ultra high performance liquid chromatography-electrospray ionization-tandem mass spectrometry and pharmacokinetic analysis of justicidin B and 6′-hydroxy justicidin C in rats". Journal of Separation Science 40, n.º 3 (29 de diciembre de 2016): 604–11. http://dx.doi.org/10.1002/jssc.201600961.
Texto completoPark, Ju-Eun, Juyeun Lee, Seung-Yong Seo y Dongyun Shin. "Regioselective route for arylnaphthalene lactones: convenient synthesis of taiwanin C, justicidin E, and daurinol". Tetrahedron Letters 55, n.º 4 (enero de 2014): 818–20. http://dx.doi.org/10.1016/j.tetlet.2013.12.014.
Texto completoHitotsuyanagi, Yukio, Masatsugu Kobayashi, Masamoto Fukuyo, Koichi Takeya y Hideji Itokawa. "A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans chinensin, justicidin B, and Taiwanin C". Tetrahedron Letters 38, n.º 48 (diciembre de 1997): 8295–96. http://dx.doi.org/10.1016/s0040-4039(97)10204-0.
Texto completoPark, Ju-Eun, Juyeun Lee, Seung-Yong Seo y Dongyun Shin. "ChemInform Abstract: Regioselective Route for Arylnaphthalene Lactones: Convenient Synthesis of Taiwanin C (I), Justicidin E (II), and Daurinol (III)." ChemInform 45, n.º 28 (26 de junio de 2014): no. http://dx.doi.org/10.1002/chin.201428220.
Texto completoHITOTSUYANAGI, Y., M. KOBAYASHI, M. FUKUYO, K. TAKEYA y H. ITOKAWA. "ChemInform Abstract: A Facile Synthesis of the 4-Aza-Analogues of 1-Arylnaphthalene Lignans Chinensin, Justicidin B, and Taiwanin C." ChemInform 29, n.º 7 (24 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199807171.
Texto completoAl-Abdallat, Ayed M., Batool K. Adayileh, Jamal S. Sawwan, Rida Shibli, Tamara S. Al-Qudah, Bashaer Abu-Irmaileh, Randa N. Albdaiwi, Jehad Almaliti y Yasser Bustanji. "Secondary Metabolites Profiling, Antimicrobial and Cytotoxic Properties of Commiphora gileadensis L. Leaves, Seeds, Callus, and Cell Suspension Extracts". Metabolites 13, n.º 4 (10 de abril de 2023): 537. http://dx.doi.org/10.3390/metabo13040537.
Texto completoSeko, Shinzo, Yoo Tanabe y Gohfu Suzukamo. "A novel synthesis of α- and β-halonaphthalenes via regioselective ring cleavage of aryl(gem-dihalocyclopropyl)methanols and its application to total synthesis of lignan lactones, justicidin e and taiwanin c". Tetrahedron Letters 31, n.º 47 (enero de 1990): 6883–86. http://dx.doi.org/10.1016/s0040-4039(00)97197-1.
Texto completoBoluda, Carlos José, José Piñero, Marialina Romero, María Gabriela Cabrera-Serra, Basilio Valladares, Zulma Aragón, Hermelo López, José A. Pérez y Juan M. Trujillo. "Anti-leishmanial Activity of Justicidone and its Synthetic Precursors". Natural Product Communications 2, n.º 2 (febrero de 2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200212.
Texto completoBoluda, Carlos J., Juan M. Trujillo, José A. Pérez, Hermelo López, Zulma Aragón y Raquel G. Díaz. "Semisynthesis of Justicidone and a 1,2-Quinone Lignan. Cytotoxic Activity of Some Natural and Synthetic Lignans". Natural Product Communications 4, n.º 2 (febrero de 2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400214.
Texto completoKOBAYASHI, K., Y. KANNO, S. SEKO y H. SUGINOME. "ChemInform Abstract: Photoinduced Molecular Transformations. Part 135. New Synthesis of Taiwanin C and Justicidin E Based on a Radical Cascade Process Involving β-Scission of Alkoxyl Radicals Generated from 3- and 8- Aryl-1-ethyl-1,2-dihydrocyclobuta(b)na". ChemInform 24, n.º 12 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199312257.
Texto completoTesis sobre el tema "Justicidin C"
Ourhzif, El-Mahdi. "Synthèse et évaluation pharmacologique de composés originaux de la famille des méthoxynaphtalènes et lignanes arylnaphtalènes à visée antitumorale". Electronic Thesis or Diss., Université Clermont Auvergne (2021-...), 2022. http://www.theses.fr/2022UCFAC016.
Texto completoBreast cancer is the most common malignant tumor in women, and the first in terms of incidence (2.1 million new cases worldwide in 2018). An increasing problem is the resistance of some cancer cells to different treatments. Due to its major impact on the population, this disease represents a critical public health problem that requires additional research at the molecular level in order to define specific therapies. The plant kingdom remains an essential source for many researchers in order to find new biologically active molecules, which can lead to the discovery of active ingredients. It is in this approach that the work carried out by our research group, in the field of the extraction and synthesis of analgesic and anticancer substances from plants used in traditional pharmacopoeia, led us to consider serial pharmacomodulations on analogues of « Guieranone A », a natural molecule isolated from the leaves of the Guiera senegalensis plant which is widely used in traditional African medicine for its therapeutic properties and which has remarkable antiproliferative activities on various tumor lines and in particular on breast cancer (MCF-7 hormone-dependent line, IC50 = 3.42 ± 0.090 µM). We have therefore developed a synthetic approach using 3,4-dimethoxy benzaldehyde as a starting material and involving Stobbe and Wittig-Horner-Emmons reactions. The synthetic reactions developed on this basis, as well as the molecules prepared, have opened a synthetic route to lignans and aza-lignans, compounds of biological and / or pharmacological interest well represented in many aromatic and medicinal plants (AMP), of the genus Justicia and Vitex. By this way, Justicidin C, Cilinaphthalide B, and Methoxy-vitedoamine A were prepared via a chloroformylation reaction followed by a Suzuki-Miyaura coupling reaction