Gotowa bibliografia na temat „Justicidine C”
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Artykuły w czasopismach na temat "Justicidine C"
Boluda, Carlos José, José Piñero, Marialina Romero, María Gabriela Cabrera-Serra, Basilio Valladares, Zulma Aragón, Hermelo López, José A. Pérez i Juan M. Trujillo. "Anti-leishmanial Activity of Justicidone and its Synthetic Precursors". Natural Product Communications 2, nr 2 (luty 2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200212.
Pełny tekst źródłaBoluda, Carlos J., Juan M. Trujillo, José A. Pérez, Hermelo López, Zulma Aragón i Raquel G. Díaz. "Semisynthesis of Justicidone and a 1,2-Quinone Lignan. Cytotoxic Activity of Some Natural and Synthetic Lignans". Natural Product Communications 4, nr 2 (luty 2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400214.
Pełny tekst źródłaLuo, Jiaoyang, Yichen Hu, Jia'an Qin i 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, nr 3 (29.12.2016): 604–11. http://dx.doi.org/10.1002/jssc.201600961.
Pełny tekst źródłaPark, Ju-Eun, Juyeun Lee, Seung-Yong Seo i Dongyun Shin. "Regioselective route for arylnaphthalene lactones: convenient synthesis of taiwanin C, justicidin E, and daurinol". Tetrahedron Letters 55, nr 4 (styczeń 2014): 818–20. http://dx.doi.org/10.1016/j.tetlet.2013.12.014.
Pełny tekst źródłaHitotsuyanagi, Yukio, Masatsugu Kobayashi, Masamoto Fukuyo, Koichi Takeya i Hideji Itokawa. "A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans chinensin, justicidin B, and Taiwanin C". Tetrahedron Letters 38, nr 48 (grudzień 1997): 8295–96. http://dx.doi.org/10.1016/s0040-4039(97)10204-0.
Pełny tekst źródłaPark, Ju-Eun, Juyeun Lee, Seung-Yong Seo i Dongyun Shin. "ChemInform Abstract: Regioselective Route for Arylnaphthalene Lactones: Convenient Synthesis of Taiwanin C (I), Justicidin E (II), and Daurinol (III)." ChemInform 45, nr 28 (26.06.2014): no. http://dx.doi.org/10.1002/chin.201428220.
Pełny tekst źródłaHITOTSUYANAGI, Y., M. KOBAYASHI, M. FUKUYO, K. TAKEYA i H. ITOKAWA. "ChemInform Abstract: A Facile Synthesis of the 4-Aza-Analogues of 1-Arylnaphthalene Lignans Chinensin, Justicidin B, and Taiwanin C." ChemInform 29, nr 7 (24.06.2010): no. http://dx.doi.org/10.1002/chin.199807171.
Pełny tekst źródłaAl-Abdallat, Ayed M., Batool K. Adayileh, Jamal S. Sawwan, Rida Shibli, Tamara S. Al-Qudah, Bashaer Abu-Irmaileh, Randa N. Albdaiwi, Jehad Almaliti i Yasser Bustanji. "Secondary Metabolites Profiling, Antimicrobial and Cytotoxic Properties of Commiphora gileadensis L. Leaves, Seeds, Callus, and Cell Suspension Extracts". Metabolites 13, nr 4 (10.04.2023): 537. http://dx.doi.org/10.3390/metabo13040537.
Pełny tekst źródłaSeko, Shinzo, Yoo Tanabe i 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, nr 47 (styczeń 1990): 6883–86. http://dx.doi.org/10.1016/s0040-4039(00)97197-1.
Pełny tekst źródłaKOBAYASHI, K., Y. KANNO, S. SEKO i 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, nr 12 (20.08.2010): no. http://dx.doi.org/10.1002/chin.199312257.
Pełny tekst źródłaRozprawy doktorskie na temat "Justicidine 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.
Pełny tekst źródłaBreast 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