Relevant bibliographies by topics / 3’- chalcone

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic '3’- chalcone'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "3’- chalcone"

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Çelik, Gonca. "New chalcone-3-O-glycoside derivatives: Synthesis and characterization." Journal of Chemical Research 44, no. 9-10 (2020): 598–601. http://dx.doi.org/10.1177/1747519820915165.

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Seven novel carbohydrate conjugates of new chalcone-3- O-glycosides were synthesized and characterized. Starting from the substituted 3′-hydroxyarylmethylacetophenone derivatives (chalcones) with α-acetobromoglucose in anhydrous acetone were synthesized 2,3,4,6-tetra- O-acetyl-3′- O-β-d-glucopyranosyloxychalcones. Deblocking the latter with CH3ONa in dry methanol results in substituted chalcone-3- O-glycosides (3′- O-β-d-glucopyranosyloxychalcones). The structures of the newly synthesized chalcone-3- O-glycosides were characterized based on 1H nuclear magnetic resonance, 13C nuclear magnetic r
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Novilla, Arina, Mustofa Mustofa, Indwiani Astuti, Jumina Jumina, and Hery Suwito. "Cytotoxic Activity of Methoxy-4’amino Chalcone Derivatives Against Leukemia Cell Lines." Molecular and Cellular Biomedical Sciences 3, no. 1 (2019): 34. http://dx.doi.org/10.21705/mcbs.v3i1.44.

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Background: Chemotherapy is a common treatment for leukemia as well as in other cancer treatment. The lack of tumor selectivity and development of multi-drug resistance by chemotherapy caused the development of new strategy in cancer treatment become a pressing need. This study was performed to evaluate the anticancer activity and selectivity of seven derivatives of chalcones against K562 and HL-60 leukemia cell lines. Materials and Methods: The cytotoxicity of chalcone’s seven derivatives (compound 1-7) was tested by using MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxyme-thoxyphenyl)-2-(4-sul
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Ali, R., A. Rahim, and A. Islam. "Synthesis and Antimicrobial Activity of 7-Hydroxy-3',4'-Methylenedioxy- and 7-Benzyloxy-3',4'-Methylenedioxy Flavanones." Journal of Scientific Research 9, no. 3 (2017): 297–306. http://dx.doi.org/10.3329/jsr.v9i3.31229.

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7-Hydroxy-3',4'-methylenedioxy- and 7-benzyloxy-3',4'-methylenedioxy flavanones have been synthesized starting from 2,4-dihydroxyacetophenone. Subsequently biocidal activities of the flavanones have been investigated along with their corresponding chalcones against some bacterial and fungal strains. 2'-Hydroxy-4'-benzyloxy-3,4-methylenedioxy chalcone (5) and its corresponding flavanone (7) showed good antibacterial and antifungal activities against some selected bacterial and fungal strains. On the other hand, 2',4'-dihydroxy-3,4-methylenedioxy chalcone (4) showed no antibacterial and antifung
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Lukovic, Jovan, Marina Mitrovic, Ivanka Zelen, Petar Čanovic, Milan Zaric, and Ivana Nikolic. "Antitumor Effect of the Chalcone Analogue, (E) -1-(4-Ethoxy-3-Methoxyphenyl) -5- Methylhex-1-En-3-One on HeLa Cell Line." Serbian Journal of Experimental and Clinical Research 20, no. 3 (2019): 215–21. http://dx.doi.org/10.2478/sjecr-2018-0048.

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Abstract Chalcones represent precursor compounds for flavonoids biosynthesis in plants. Chalcones, 1,3-diaryl-2-propen-1-ones, have unique chemical structure with conjugated double bonds and delocalized π-electron system on both aromatic rings. Various studies have shown that chemical structure of chalcone is responsible for their antitumor effect. In our study, we have examined the antitumor effect of chalcone analogue (E) -1- (4-ethoxy-3-methoxyphenyl) -5-methylhex-1-en-3-one (CH) on HeLa cells. The antitumor efficiency of different CH concentrations was compared to the antitumor effects of
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Tantawy, Mohamed A., Farid M. Sroor, Magda F. Mohamed, et al. "Molecular Docking Study, Cytotoxicity, Cell Cycle Arrest and Apoptotic Induction of Novel Chalcones Incorporating Thiadiazolyl Isoquinoline in Cervical Cancer." Anti-Cancer Agents in Medicinal Chemistry 20, no. 1 (2020): 70–83. http://dx.doi.org/10.2174/1871520619666191024121116.

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Background: Chalcones are naturally occurring compounds found in various plant species which are widely used for the traditional popular treatments. Chalcones are distinguished secondary metabolites that are reported to display diverse biological activities such as antiviral, antiplatelet, anti-inflammatory, anticancer, antibacterial and antioxidant agents. The presence of a,ß-unsaturated carbonyl group in chalcones is assumed to be responsible for their bioactivity. In addition, heterocyclic compounds having nitrogen such as isoquinolines are of considerable interest as they constitute the co
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Coskun, Demet, Misir Ahmedzade, and Sevda Kirbag. "3-(Substituted Aryl)-1-benzofuranyl-2-propenones: Antimicrobial Properties of Some Chalcones-Type Compounds and their 2-Pyrazoline Derivatives." E-Journal of Chemistry 8, no. 4 (2011): 1574–81. http://dx.doi.org/10.1155/2011/806854.

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2-Acetylbenzofuran on condensation with furan-2-carboxaldehyde and pyrrole-2-carboxaldehyde in methanolic KOH solution yielded the corresponding benzofuran chalcones. These two compounds and nine benzofuran chalcones were synthesized before, were further reacted with hydrazine hydrate in ethanol which led to the formation of 2-pyrazoline derivatives. All the synthesized compounds were characterized by elemental analysis, melting point determination, infrared spectroscopy and nuclear magnetic resonance spectroscopy. Nine chalcone-type compounds and eleven 2-pyrazolines were evaluated for their
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Coşkun, Demet, Suat Tekin, Süleyman Sandal, and Mehmet Fatih Coşkun. "Synthesis, Characterization, and Anticancer Activity of New Benzofuran Substituted Chalcones." Journal of Chemistry 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/7678486.

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Benzofuran derivatives are of great interest in medicinal chemistry and have drawn considerable attention due to their diverse pharmacological profiles including anticancer activity. Similarly, chalcones, which are common substructures of numerous natural products belonging to the flavonoid class, feature strong anticancer properties. A novel series of chalcones, 3-aryl-1-(5-bromo-1-benzofuran-2-yl)-2-propanones propenones (3a–f), were designed, synthesized, and characterized.In vitroantitumor activities of the newly synthesized (3a–f) and previously synthesized (3g–j) chalcone compounds were
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Rezende-Júnior, Luís Mário, Leila Maria de Sousa Andrade, Antonio Linkoln Alves Borges Leal, et al. "Chalcones Isolated from Arrabidaea brachypoda Flowers as Inhibitors of NorA and MepA Multidrug Efflux Pumps of Staphylococcus aureus." Antibiotics 9, no. 6 (2020): 351. http://dx.doi.org/10.3390/antibiotics9060351.

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Bacterial resistance to antibiotics has become a public health issue around the world. The present study aimed to evaluate the antibacterial activity of chalcones isolated from flowers of Arrabidaea brachypoda, and their potential as efflux pump inhibitors of Staphylococcus aureus efflux pumps. Microdilution assays were performed with natural products from A. brachypoda. Chalcones 1, 3, 4, and 5 did not show intrinsic antimicrobial activity against all S. aureus strains tested, but they were able to potentiate the Norfloxacin action against the SA1199-B (norA) strain, with a better modulating
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Zhao, Haiying, Xueyou Zhu, Dong Wang, Shufeng Chen, and Zhanxi Bian. "Synthesis, Electrochemical, and Thermal Properties of [3]Ferrocenophane-Containing Chalcone Derivatives." Australian Journal of Chemistry 68, no. 7 (2015): 1035. http://dx.doi.org/10.1071/ch14529.

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[3]Ferrocenophane-containing chalcone derivatives with benzene ring (3a–3d) or naphthalene ring (3e–3f) were synthesized and characterized. The potentials for [3]ferrocenophane-containing chalcones cathodically shifted ~70–80 mV compared with those of ferrocene-containing chalcones, indicating easier oxidation by loss of an electron for the former. The thermal behaviours of the prepared compounds were studied by differential scanning calorimetry and polarizing optical microscopy. Compound 3f with terminal alkyl chain of 14 carbon atoms displayed mesophases, whereas other compounds were non-mes
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Sweeting, Stephen G., Charlie L. Hall, Jason Potticary, et al. "The solubility and stability of heterocyclic chalcones compared with trans-chalcone." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 1 (2020): 13–17. http://dx.doi.org/10.1107/s2052520619015907.

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Heterocyclic chalcones are a recently explored subgroup of chalcones that have sparked interest due to their significant antibacterial and antifungal capabilities. Herein, the structure and solubility of two such compounds, (E)-1-(1H-pyrrol-2-yl)-3-(thiophen-2-yl)prop-2-en-1-one and (E)-3-phenyl-1-(1H-pyrrol-2-yl)prop-2-en-1-one, are assessed. Single crystals of (E)-1-(1H-pyrrol-2-yl)-3-(thiophen-2-yl)prop-2-en-1-one were grown, allowing structural comparisons between the heterocyclic chalcones and (2E)-1,3-diphenylprop-2-en-1-one, trivially known as trans-chalcone. The two heterocyclic chalco
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Dissertations / Theses on the topic "3’- chalcone"

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Cerrejón-Palanco, Ana. "Desenvolvimento de protótipos antifúngicos contra Cryptococcus gattii utilizando modelos alternativos animais." Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/144294.

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Submitted by ANA CERREJÓN PALANCO null (anacerrejon@live.com) on 2016-09-29T21:40:59Z No. of bitstreams: 1 Mestrado-Ana-Cerrejón-Palanco.pdf: 2202083 bytes, checksum: 3d49fc49aae6a457cad301dea9e43240 (MD5)<br>Approved for entry into archive by Juliano Benedito Ferreira (julianoferreira@reitoria.unesp.br) on 2016-10-04T19:11:41Z (GMT) No. of bitstreams: 1 carrejonpalanco_a_me_arafcf.pdf: 2202083 bytes, checksum: 3d49fc49aae6a457cad301dea9e43240 (MD5)<br>Made available in DSpace on 2016-10-04T19:11:41Z (GMT). No. of bitstreams: 1 carrejonpalanco_a_me_arafcf.pdf: 2202083 bytes, checksum: 3d49
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Morand, Jean-Marc. "Étude métabolique de l'aza-3 chalcol (10184 CERM) chez le rat." Université Joseph Fourier (Grenoble), 1989. http://www.theses.fr/1989GRE18001.

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COSTA, José Elierson Barros. "Efeito antineoplásico do composto 4,2´,3´,4´-tetrametoxi chalcona em linhagem de neuroblastoma B103 de rato." Universidade Federal do Pará, 2014. http://repositorio.ufpa.br/jspui/handle/2011/5942.

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Submitted by Cleide Dantas (cleidedantas@ufpa.br) on 2014-10-30T11:55:11Z No. of bitstreams: 2 license_rdf: 22974 bytes, checksum: 99c771d9f0b9c46790009b9874d49253 (MD5) Dissertacao_EfeitoAntineoplasicoComposto.pdf: 1843144 bytes, checksum: 2c1a12d9e05779f464daf3de28979f2c (MD5)<br>Approved for entry into archive by Ana Rosa Silva (arosa@ufpa.br) on 2014-10-30T13:57:12Z (GMT) No. of bitstreams: 2 license_rdf: 22974 bytes, checksum: 99c771d9f0b9c46790009b9874d49253 (MD5) Dissertacao_EfeitoAntineoplasicoComposto.pdf: 1843144 bytes, checksum: 2c1a12d9e05779f464daf3de28979f2c (MD5)<br>Made av
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Cordeiro, Marlon Norberto Sechini. "Síntese, caracterização e avaliação da atividade biológica de nitrichalconas e de chalconas derivadas da 6-acetil-2h-1,4-benzoxazin-3(4H)-ona." reponame:Repositório Institucional da UFSC, 2013. https://repositorio.ufsc.br/xmlui/handle/123456789/122776.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciencias Fisicas e Matemáticas, Programa de Pós-Graduação em Química, Florianópolis, 2013.<br>Made available in DSpace on 2014-08-06T17:21:39Z (GMT). No. of bitstreams: 1 325488.pdf: 3321580 bytes, checksum: 54d833ad499c25ebc1352a3008f4dce1 (MD5) Previous issue date: 2013<br>Este trabalho teve como objetivo a síntese e caracterização de duas séries de chalconas, uma derivada da CH8 (previamente patenteada pelo grupo), contendo o grupo nitro na posição 3 ou 3' (série ML) e a outra derivada da 6-acetil-2H-1,4-benzoxazin
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Yauri, Cruz Carlos Alberto. "Evaluación de la actividad in vitro de 3 chalconas sintéticas contra parásitos intracelulares de Leishmania infantum." Bachelor's thesis, Universidad Nacional Mayor de San Marcos, 2019. https://hdl.handle.net/20.500.12672/11122.

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Determina la actividad anti-Leishmania de tres chalconas de origen sintético contra parásitos de Leishmania infantum, causantes de leishmaniosis visceral. La identidad de las chalconas fue confirmada a través de espectros RMN de protón y fueron etiquetadas como “chalcona 40”, “chalcona 4β” y “chalcona 4γ”. Se desarrollaron tres modelos de evaluación in vitro los cuales emplearon promastigotes procíclicos, amastigotes axénicos y amastigotes intramacrofágicos. Adicionalmente se evaluó la citotoxicidad de los compuestos utilizando macrófagos peritoneales de ratón BALB/C y la línea celular “Raw Ce
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Mousinho, Kristiana Cerqueira. "Estudo do Potencial AnticÃncer de um Derivado de Chalcona, 1-(4-Nitrofenil)-3-Fenilprop-2-En-1-Ona, In vitro e In vivo." Universidade Federal do CearÃ, 2010. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=10509.

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CoordenaÃÃo de AperfeiÃoamento de NÃvel Superior<br>A substÃncia 1-(4-Nitrofenil)-3-fenilprop-2-en-1-ona (CG) Ã um derivado de chalcona, sintetizado a partir da reaÃÃo quÃmica entre a acetofenona e para-nitro benzaldeÃdo. Para avaliar o seu potencial anticÃncer foi realizado um estudo farmacolÃgico de suas propriedades antitumorais em vÃrios modelos biolÃgicos in vitro e in vivo. A CG apresentou potente atividade citotÃxica nas 5 linhagens tumorais testadas, inibindo a proliferaÃÃo das cÃlulas tumorais pelo ensaio do MTT e em cÃlulas mononucleares do sangue perifÃrico (PMCB) humano atravÃs do
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Mousinho, Kristiana Cerqueira. "Estudo do potencial anticâncer de um derivado de Chalcona, 1-(4-Nitrofenil)-3-Fenilprop-2-En-1-Ona, in vitro e in vivo." reponame:Repositório Institucional da UFC, 2010. http://www.repositorio.ufc.br/handle/riufc/5787.

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MOUSINHO, Kristiana Cerqueira. Estudo do potencial anticâncer de um derivado de Chalcona, 1-(4-Nitrofenil)-3-Fenilprop-2-En-1-Ona, in vitro e in vivo. 2010. 170 f. Tese (Doutorado em Farmacologia) - Universidade Federal do Ceará. Faculdade de Medicina, Fortaleza, 2010.<br>Submitted by denise santos (denise.santos@ufc.br) on 2013-09-11T13:50:16Z No. of bitstreams: 1 2012_tese_kcmousinho.pdf: 6059203 bytes, checksum: 15a549b1f793c7ea358dc9fbab7fb2cb (MD5)<br>Approved for entry into archive by denise santos(denise.santos@ufc.br) on 2013-09-11T16:40:53Z (GMT) No. of bitstreams: 1 2012_tese_kcmous
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GRISCOM, LAURENT. "Synthese et proprietes optiques des verres de chalco-halogenures : spectroscopie a 1,3 microns et addition de photons des ions nd 3 + et pr 3 +." Rennes 1, 1999. http://www.theses.fr/1999REN10191.

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Des sources lumineuses sont, a ce jour activement recherchees a 1,3 m pour augmenter la capacite des reseaux de telecommunications par fibres optiques. Pour cela, des compositions de verres dopes aux terres rares et optimises du point de leurs proprietes optiques sont necessaires. Les verres de chalcogenures ayant des indices de refraction eleves et une transparence dans l'infrarouge qui s'etend au-dela de 10 m possedent les qualites necessaires pour operer a cette longueur d'onde. Les verres de chalco-halogenures, avec les elements ge-ga-s-csx ou x = c1, br, i ont ete synthetise au laboratoir
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Maluleka, Marole Maria. "Synthesis, biological evaluation and molecular docking studies of novel indole- and benzofuran-chalcone and benzofuran-quinazoline hybrids as anticancer agents." Thesis, 2019. http://hdl.handle.net/10500/25821.

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Text in English<br>Specially prepared 2-amino-5-bromo-3-iodoacetophenone and 5-bromo-2-hydroxy-3 iodoacetophenone were subjected to Claisen-Schmidt aldol condensation with benzaldehyde derivatives followed by sequential and/or one-pot palladium catalyzed Sonogashira cross coupling and heteroannulation of the 3-alkynylated intermediates to afford indole-chalcones and benzofuran-chalcones, respectively. The indole-chalcones derivatives were, in turn, subjected to trifluoroacetic anhydride in tetrahydrofuran under reflux to afford the corresponding 3-trifluoroacetyl substituted indole-chalcone d
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Huang, Chun-Chang, and 黃俊彰. "Synthesis of Naturally Occurring Chalcones Containing 2-Hydroxy-3-methylbut-3-enyl Group." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/46447875158362080023.

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Book chapters on the topic "3’- chalcone"

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Schomburg, Dietmar, and Dörte Stephan. "Naringenin-chalcone synthase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_206.

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Seitz, H. U., and J. Gleitz. "Regulation of Chalcone Synthase with Regard to Anthocyanin Biosynthesis." In Primary and Secondary Metabolism of Plant Cell Cultures II. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74551-5_10.

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Ninomiya, Masayuki, and Mamoru Koketsu. "Minor Flavonoids (Chalcones, Flavanones, Dihydrochalcones, and Aurones)." In Natural Products. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_62.

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Lenardão, Eder João, Claudio Santi, and Luca Sancineto. "Nonbonded Interaction: The Chalcogen Bond." In New Frontiers in Organoselenium Compounds. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-92405-2_4.

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Iwaoka, Michio. "Chalcogen Bonds in Protein Architecture." In Challenges and Advances in Computational Chemistry and Physics. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14163-3_9.

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"4,2′-Dihydroxy-6″,6″-dimethylpyrano[2″,3″,4′,3′]-chalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1073.

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"2′-Hydroxy-4-methoxyfurano (3′,4′-4″,5″) chalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1070.

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"2′-Hydroxy-4,5′-dimethoxyfurano (3′,4′-4″,5″) chalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1071.

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"Melafolone (2′,4′-Dihydroxy-3′,6′-dimethoxy-5′-(2-methylbutyryloxy) chalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1069.

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"4-Benzyloxy-2′-hydroxy-5′-methoxyfurano (3′,4′-4″,5″) chalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1072.

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Conference papers on the topic "3’- chalcone"

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Wang, Luyao, Hongye Zhao, Dan Wu, Long Qin, Yuou Teng, and Kui Lu. "Synthesis and biological evaluation of the novel antitumor agent 3'-monosubstituted chalcone derivatives." In 3rd International Conference on Material, Mechanical and Manufacturing Engineering (IC3ME 2015). Atlantis Press, 2015. http://dx.doi.org/10.2991/ic3me-15.2015.101.

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Aguiar, Antônio S. N., Jaqueline E. Queiroz, Pollyana P. Firmino, et al. "Experimental and theoretical study of the chalcone molecule (E)-3-(2,6-difluorophenyl)-1-(furan-2-yl)-prop-2-en-1-one." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202033.

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In this work, we synthesized chalcone (E)-3-(2,6-difluorophenyl)-1-(furan-2-yl)-prop-2-en-1-one (DTP) via Claisen-Schmidt condensation. The supramolecular arrangement of the obtained compound was characterized by X-ray diffraction and Hirshfeld surface, and its crystalline structure was determined. The DTP molecule was studied using the Density Functional Theory, at the theoretical level M06-2X/6-311G ++G, in order to obtain information about its structural and electronic properties. A map of molecular electrostatic potential was obtained to predict the types of interactions and their acid-bas
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Arianingrum, Retno, and Indyah Sulistyo Arty. "The effect of bromo chalcone [1-(4’-bromophenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propene-1-on] on T47D breast cancer cells." In 2ND INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). Author(s), 2018. http://dx.doi.org/10.1063/1.5065031.

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Tippin, Matthew A., Dong Jun Fu, Liankun Song, Victor Pham, and Xaolin Zi. "Abstract 5083: BSCHL-2046, a lead chalcone derivative from a newly synthesized library, is a potent neddylation inhibitor against the growth of prostate cancer cell lines." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-5083.

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Tippin, Matthew A., Dong Jun Fu, Liankun Song, Victor Pham, and Xaolin Zi. "Abstract 5083: BSCHL-2046, a lead chalcone derivative from a newly synthesized library, is a potent neddylation inhibitor against the growth of prostate cancer cell lines." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-5083.

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Liu, Zhongbo, Xuesen Li, Anna Simoneau, and Xiaolin Zi. "Abstract 5678: Kavalactone yangonin induces autophagy, inhibits TSC-mediated translation initiation and acts synergistically with a kava chalcone flavokawain A on growth inhibition in bladder cancer UMUC-3 cells." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-5678.

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Shutalev, Anatoly, Anastasia Fesenko, and Pavel Solovyev. "Addition of Thiocyanic Acid to Chalcones: Practical Synthesis of 1,3-Diaryl-3-isothiocyanatopropan-1-ones." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a017.

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Zhang, Tianshun, Qiushi Wang, Hitoshi Ashida, Ann Bode, and Zigang Dong. "Abstract 4798: The Ashitaba (Angelica keiskei) chalcones 4-hydroxyderricin and xanthoangelol suppress melanomagenesis by targeting BRAF and PI3-K." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-4798.

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Zhang, Tianshun, Qiushi Wang, Hitoshi Ashida, Ann Bode, and Zigang Dong. "Abstract 4798: The Ashitaba (Angelica keiskei) chalcones 4-hydroxyderricin and xanthoangelol suppress melanomagenesis by targeting BRAF and PI3-K." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-4798.

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Seshadri, Gayatri, Jonathan K. Chun, and Andrew B. Bocarsly. "Interfacial chemistry as a controlling element in photoinduced charge transfer in n-type cadmium chalconide/Fe(CN) 64-/3-cells (Invited Paper)." In Optical Materials Technology for Energy Efficiency and Solar Energy, edited by Anne Hugot-Le Goff, Claes-Goeran Granqvist, and Carl M. Lampert. SPIE, 1992. http://dx.doi.org/10.1117/12.130577.

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You might also be interested in the extended bibliographies on the topic '3’- chalcone' for particular source types:
Journal articles
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