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You searched for subject:(Combretastatin A 4). Showing records 1 – 8 of 8 total matches.

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NSYSU

1. Lin, Jia-ying. Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures.

Degree: Master, Chemistry, 2012, NSYSU

 A series of anilines and enediynes containing Combretastatin A-4 analogues were synthesized. The growth inhibitory activity of these analogues were evaluated against three human cancer… (more)

Subjects/Keywords: Combretastatin A-4; enediyne; aniline; IC50

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lin, J. (2012). Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0719112-113520

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lin, Jia-ying. “Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures.” 2012. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0719112-113520.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lin, Jia-ying. “Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures.” 2012. Web. 15 Apr 2021.

Vancouver:

Lin J. Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0719112-113520.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lin J. Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0719112-113520

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


NSYSU

2. Zeng, Jun-Yan. New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line.

Degree: Master, Biological Sciences, 2015, NSYSU

 Antimitotic drug, combretastatin A-4 (CA-4) is a natural plant extract exhibits powerful anticancer and anti-angiogenesis activity by targeting microtubule formation. CA-4 enediyne derivatives, such as… (more)

Subjects/Keywords: Combretastatin A-4; LO-OMe; LO-NH2; PARP; Caspase-3; Apoptosis; Autophagy; p62; LC3

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zeng, J. (2015). New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019115-165758

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zeng, Jun-Yan. “New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line.” 2015. Thesis, NSYSU. Accessed April 15, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019115-165758.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zeng, Jun-Yan. “New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line.” 2015. Web. 15 Apr 2021.

Vancouver:

Zeng J. New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line. [Internet] [Thesis]. NSYSU; 2015. [cited 2021 Apr 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019115-165758.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zeng J. New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019115-165758

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

3. Nguyen, Thi Thanh Binh. Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4.

Degree: Docteur es, Biomolécules, pharmacologie, thérapeutique, 2012, Université Claude Bernard – Lyon I

La combretastatine A-4 (CA-4), produit naturel isolé d’un arbuste d’Afrique du sud (Combretum caffrum K.), a montré des propriétés antitumorales intéressantes. Grâce à sa capacité… (more)

Subjects/Keywords: Combretastatine A-4; Dérivés hétérocycliques; Anticancer; Antitubuline; Antiprolifératif; Antimitotique; Kératinocyte; Nanoparticules lipidiques solides; Combretastatin A-4; Heterocyclic derivatives; Anticancer; Antitubuline; Antiproliferative; Antimitotic; Keratinocyte; Solid lipid nanoparticles; 615.19

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APA (6th Edition):

Nguyen, T. T. B. (2012). Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10306

Chicago Manual of Style (16th Edition):

Nguyen, Thi Thanh Binh. “Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed April 15, 2021. http://www.theses.fr/2012LYO10306.

MLA Handbook (7th Edition):

Nguyen, Thi Thanh Binh. “Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4.” 2012. Web. 15 Apr 2021.

Vancouver:

Nguyen TTB. Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2012LYO10306.

Council of Science Editors:

Nguyen TTB. Synthèse, évaluation biologique et vectorisation de dérivés hétérocycliques de la combretastatine A-4 : Synthesis, biological evaluation and vectorisation of heterocyclic derivatives of combretastatin A-4. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10306

4. BARROS, Maria Ester de Sá Barreto. Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4.

Degree: 2015, Federal University of Pernambuco

CNPQ

A primeira parte deste trabalho envolveu o estudo de docking molecular, a síntese, e a avaliação das atividades antitumorais e anti-inflamatórias de lactonas -insaturadas,… (more)

Subjects/Keywords: Docking molecular; Atividade antitumoral; -lactonas; -insaturadas; Combretastatina A-4; Z-estilbenos; Molecular docking; Anti-tumoral activity; -unsaturaded; -lactones; Combretastatin A-4; Z-stilbenes

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APA (6th Edition):

BARROS, M. E. d. S. B. (2015). Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4. (Masters Thesis). Federal University of Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/18477

Chicago Manual of Style (16th Edition):

BARROS, Maria Ester de Sá Barreto. “Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4.” 2015. Masters Thesis, Federal University of Pernambuco. Accessed April 15, 2021. https://repositorio.ufpe.br/handle/123456789/18477.

MLA Handbook (7th Edition):

BARROS, Maria Ester de Sá Barreto. “Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4.” 2015. Web. 15 Apr 2021.

Vancouver:

BARROS MEdSB. Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4. [Internet] [Masters thesis]. Federal University of Pernambuco; 2015. [cited 2021 Apr 15]. Available from: https://repositorio.ufpe.br/handle/123456789/18477.

Council of Science Editors:

BARROS MEdSB. Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4. [Masters Thesis]. Federal University of Pernambuco; 2015. Available from: https://repositorio.ufpe.br/handle/123456789/18477


University of Vienna

5. Fürst, Rita. Synthesis and biological evaluation of novel combretastatin-a4 analogs.

Degree: 2009, University of Vienna

Der Naturstoff Combretastatin A-4 (CA-4) wurde 1982 erstmals, gemeinsam mit verwandten Verbindungen aus einer afrikanischen Weidenart, Combretum caffrum, isoliert. Die Verbindung zeigt sehr starke antimitotische… (more)

Subjects/Keywords: 35.52 Präparative Organische Chemie; Combretastatin-A4 / AVE8062 / Diazomethan / Cyclopropan-Synthese / Mikrotubuli / Colchicin; Combretastatin A-4 / diazomethane / cyclopropane synthesis / AVE8062 / microtubules / colchicine

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Fürst, R. (2009). Synthesis and biological evaluation of novel combretastatin-a4 analogs. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/3911/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Fürst, Rita. “Synthesis and biological evaluation of novel combretastatin-a4 analogs.” 2009. Thesis, University of Vienna. Accessed April 15, 2021. http://othes.univie.ac.at/3911/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Fürst, Rita. “Synthesis and biological evaluation of novel combretastatin-a4 analogs.” 2009. Web. 15 Apr 2021.

Vancouver:

Fürst R. Synthesis and biological evaluation of novel combretastatin-a4 analogs. [Internet] [Thesis]. University of Vienna; 2009. [cited 2021 Apr 15]. Available from: http://othes.univie.ac.at/3911/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Fürst R. Synthesis and biological evaluation of novel combretastatin-a4 analogs. [Thesis]. University of Vienna; 2009. Available from: http://othes.univie.ac.at/3911/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Paris-Sud – Paris XI

6. Tréguier, Bret. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.

Degree: Docteur es, Chimie, 2012, Université Paris-Sud – Paris XI

Lors de son développement, une tumeur ne peut survivre sans passer par une étape invasive afin de subvenir à ses besoins en nutriment et en… (more)

Subjects/Keywords: Antivasculaire; Inhibition de la polymérisation de la tubuline; Bioisostérie; Couplage pallado-catalysé; Cyclisation; Ényne; Combretastatin A-4; Antivascular; Cytotoxicity; Tubulin polymerization inhibition; Bioisosterism; Pallado-catalyzed cross coupling; Cyclization; Enyne

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tréguier, B. (2012). Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA114805

Chicago Manual of Style (16th Edition):

Tréguier, Bret. “Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 15, 2021. http://www.theses.fr/2012PA114805.

MLA Handbook (7th Edition):

Tréguier, Bret. “Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation.” 2012. Web. 15 Apr 2021.

Vancouver:

Tréguier B. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2012PA114805.

Council of Science Editors:

Tréguier B. Développement de nouveaux analogues structuraux de l’isocombrétastatine A-4 : conception, synthèse et évaluation biologique : Development of news isocombretastatin A-4 derivatives : design, synthesis and biological evaluation. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA114805

7. Hemerson Iury Ferreira MagalhÃes. Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07).

Degree: 2009, Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em Farmacologia; UFC; BR

CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior

A fenstatina, quimicamente designada de 4-metoxifenil-3,4,5-trimetoxifenilmetanona, denominada RR07, Ã uma bisarilcetona de esqueleto estilbenÃide que pode ser… (more)

Subjects/Keywords: AntineoplÃsicos; phenstatin, combretastatin A-4; tubulin; cytotoxic; antitumor activity; FARMACOLOGIA

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APA (6th Edition):

MagalhÃes, H. I. F. (2009). Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07). (Doctoral Dissertation). Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em Farmacologia; UFC; BR. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4032

Chicago Manual of Style (16th Edition):

MagalhÃes, Hemerson Iury Ferreira. “Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07).” 2009. Doctoral Dissertation, Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em Farmacologia; UFC; BR. Accessed April 15, 2021. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4032.

MLA Handbook (7th Edition):

MagalhÃes, Hemerson Iury Ferreira. “Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07).” 2009. Web. 15 Apr 2021.

Vancouver:

MagalhÃes HIF. Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07). [Internet] [Doctoral dissertation]. Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em Farmacologia; UFC; BR; 2009. [cited 2021 Apr 15]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4032.

Council of Science Editors:

MagalhÃes HIF. Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07). [Doctoral Dissertation]. Universidade Federal do CearÃ; Programa de PÃs-GraduaÃÃo em Farmacologia; UFC; BR; 2009. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4032

8. Faouzi, Abdelfattah. Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors.

Degree: Docteur es, Chimie thérapeutique et médicinale, 2017, Lyon

 En 2015, on estime le nombre de nouveaux cas de cancer à plus de 385000 et le nombre de décès à 149500. Ces chiffres, plus… (more)

Subjects/Keywords: Cancer; Combrétastatine A-4; Antitubuline; CK2; DYRK; Indénobenzo[b]thiophène; Inhibiteurs de CK2; Inhibiteurs de DYRK; Cancer; Combretastatin A-4; Tubulin inhibitors; CK2; DYRK; Indenobenzo[b]thiophene; CK2 inhibitors; DYRK inhibitors; 570

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Faouzi, A. (2017). Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2017LYSE1233

Chicago Manual of Style (16th Edition):

Faouzi, Abdelfattah. “Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors.” 2017. Doctoral Dissertation, Lyon. Accessed April 15, 2021. http://www.theses.fr/2017LYSE1233.

MLA Handbook (7th Edition):

Faouzi, Abdelfattah. “Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors.” 2017. Web. 15 Apr 2021.

Vancouver:

Faouzi A. Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors. [Internet] [Doctoral dissertation]. Lyon; 2017. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2017LYSE1233.

Council of Science Editors:

Faouzi A. Synthèses et évaluations biologiques d’analogues de la combrétastatine A-4 et d’inhibiteurs de kinases DYRK : Syntheses and biological evaluations of combretastatine A-4 analogs and DYRK kinases inhibitors. [Doctoral Dissertation]. Lyon; 2017. Available from: http://www.theses.fr/2017LYSE1233

.