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You searched for subject:(Combretastatin). Showing records 1 – 15 of 15 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 June 17, 2019. 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. 17 Jun 2019.

Vancouver:

Lin J. Design and Synthesis of New Antitumor Agents Containing Aniline and Enediyne substructures. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Jun 17]. 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 (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 June 17, 2019. 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. 17 Jun 2019.

Vancouver:

Zeng J. New Combretastatin A-4 enediyne derivatives induce Program Cell Death in Neuroblastoma SH-SY5Y cell line. [Internet] [Thesis]. NSYSU; 2015. [cited 2019 Jun 17]. 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. Hemerson Iury Ferreira MagalhÃes. Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07).

Degree: PhD, 2009, Universidade Federal do Ceará

A fenstatina, quimicamente designada de 4-metoxifenil-3,4,5-trimetoxifenilmetanona, denominada RR07, Ã uma bisarilcetona de esqueleto estilbenÃide que pode ser obtida a partir da combretastatina A4, com reconhecida… (more)

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

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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 Ceará. 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 Ceará. Accessed June 17, 2019. 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. 17 Jun 2019.

Vancouver:

MagalhÃes HIF. Propriedades anticÃncer da fenstatina, 4-metoxifenil-3,4,5-trimetoxifenilmetanona (RR07). [Internet] [Doctoral dissertation]. Universidade Federal do Ceará 2009. [cited 2019 Jun 17]. 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 Ceará 2009. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4032 ;


University of Kentucky

4. Madadi, Nikhil Reddy. Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents.

Degree: 2014, University of Kentucky

 Resveratrol has been reported as a potential anticancer agent but cannot be used as an antitumor drug due to its chemical and metabolic instability. We… (more)

Subjects/Keywords: combretastatin; resveratrol; triazole; tetrazole; cannabinoid; Chemicals and Drugs; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Madadi, N. R. (2014). Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents. (Doctoral Dissertation). University of Kentucky. Retrieved from http://uknowledge.uky.edu/pharmacy_etds/42

Chicago Manual of Style (16th Edition):

Madadi, Nikhil Reddy. “Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents.” 2014. Doctoral Dissertation, University of Kentucky. Accessed June 17, 2019. http://uknowledge.uky.edu/pharmacy_etds/42.

MLA Handbook (7th Edition):

Madadi, Nikhil Reddy. “Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents.” 2014. Web. 17 Jun 2019.

Vancouver:

Madadi NR. Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2019 Jun 17]. Available from: http://uknowledge.uky.edu/pharmacy_etds/42.

Council of Science Editors:

Madadi NR. Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: http://uknowledge.uky.edu/pharmacy_etds/42


Baylor University

5. Nguyen, Benson Lee. Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer.

Degree: Chemistry and Biochemistry., 2011, Baylor University

 Cancer is the second leading cause of death in the United States with over 550,000 deaths in 2009 and a devastating 7.9 million deaths worldwide… (more)

Subjects/Keywords: Combretastatin A-1 analogs.; Small molecule vascular disrupting agents.; Bioreductive triggers.; Cancer treatment.; Chemistry.

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APA (6th Edition):

Nguyen, B. L. (2011). Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/8092

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):

Nguyen, Benson Lee. “Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer. ” 2011. Thesis, Baylor University. Accessed June 17, 2019. http://hdl.handle.net/2104/8092.

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

MLA Handbook (7th Edition):

Nguyen, Benson Lee. “Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer. ” 2011. Web. 17 Jun 2019.

Vancouver:

Nguyen BL. Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer. [Internet] [Thesis]. Baylor University; 2011. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2104/8092.

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

Council of Science Editors:

Nguyen BL. Design and synthesis of combretastatin A-1 analogs, small molecule vascular disrupting agents, and bioreductive triggers as potential therapeutic agents for the treatment of cancer. [Thesis]. Baylor University; 2011. Available from: http://hdl.handle.net/2104/8092

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


Baylor University

6. [No author]. Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia.

Degree: 2018, Baylor University

 The tumor microenvironment provides a number of promising targets for selective treatment with anticancer agents. Aberrant tumor-associated neovascularization offers one such targeting opportunity. Compounds referred… (more)

Subjects/Keywords: Vascular disrupting agents. Combretastatin A-4. Indole. Hypoxia. Bioreductively activatable prodrug conjugates.

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APA (6th Edition):

author], [. (2018). Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/10433

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):

author], [No. “Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia. ” 2018. Thesis, Baylor University. Accessed June 17, 2019. http://hdl.handle.net/2104/10433.

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

MLA Handbook (7th Edition):

author], [No. “Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia. ” 2018. Web. 17 Jun 2019.

Vancouver:

author] [. Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia. [Internet] [Thesis]. Baylor University; 2018. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2104/10433.

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

Council of Science Editors:

author] [. Small-molecule inhibitors of tubulin polymerization as vascular disrupting agents and prodrugs targeting tumor-associated hypoxia. [Thesis]. Baylor University; 2018. Available from: http://hdl.handle.net/2104/10433

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

7. Cucca, Mélissa. Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis.

Degree: Docteur es, Chimie Organique, 2018, Clermont Auvergne

L'angiogénèse est un phénomène vital dans de nombreux processus physiologiques tels que le développement embryonnaire ou la cicatrisation. Mais c'est aussi un processus pathologique impliqué… (more)

Subjects/Keywords: VDA; Agents perturbateurs vasculaires; Arthrose; Ostéoarthrite; Angiogenèse; Néovascularisation; E7010; Combrétastatine A4; VDA; Oseoarthritis; Angiogenesis; E7010; Combretastatin A4

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

APA (6th Edition):

Cucca, M. (2018). Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis. (Doctoral Dissertation). Clermont Auvergne. Retrieved from http://www.theses.fr/2018CLFAC008

Chicago Manual of Style (16th Edition):

Cucca, Mélissa. “Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis.” 2018. Doctoral Dissertation, Clermont Auvergne. Accessed June 17, 2019. http://www.theses.fr/2018CLFAC008.

MLA Handbook (7th Edition):

Cucca, Mélissa. “Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis.” 2018. Web. 17 Jun 2019.

Vancouver:

Cucca M. Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis. [Internet] [Doctoral dissertation]. Clermont Auvergne; 2018. [cited 2019 Jun 17]. Available from: http://www.theses.fr/2018CLFAC008.

Council of Science Editors:

Cucca M. Conception, synthèse et évaluation in vitro de nouveaux agents perturbateurs vasculaires pour le traitement de l'arthrose : Design, synthesis and in vitro evaluation of news vascular disrupting agents for the treatment of osteoarthritis. [Doctoral Dissertation]. Clermont Auvergne; 2018. Available from: http://www.theses.fr/2018CLFAC008


University of Vienna

8. 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 (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 June 17, 2019. 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. 17 Jun 2019.

Vancouver:

Fürst R. Synthesis and biological evaluation of novel combretastatin-a4 analogs. [Internet] [Thesis]. University of Vienna; 2009. [cited 2019 Jun 17]. 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

9. 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, Universidade Federal de Pernambuco

 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, análogos… (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 . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/18477

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):

BARROS, Maria Ester de Sá Barreto. “Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4 .” 2015. Thesis, Universidade Federal de Pernambuco. Accessed June 17, 2019. http://repositorio.ufpe.br/handle/123456789/18477.

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

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. 17 Jun 2019.

Vancouver:

BARROS MEdSB. Estudos de Docking Molecular, síntese e atividade biológica de análogos da (-)- massoialactona e da combretastatina A-4 . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2015. [cited 2019 Jun 17]. Available from: http://repositorio.ufpe.br/handle/123456789/18477.

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

Council of Science Editors:

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

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

10. 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 June 17, 2019. 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. 17 Jun 2019.

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 2019 Jun 17]. 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


University of Pennsylvania

11. Levine, Dalia H. POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS.

Degree: 2010, University of Pennsylvania

 ABSTRACT POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS Dalia Hope Levine Dr. Daniel A. Hammer Nanoparticles are currently being developed as delivery vehicles… (more)

Subjects/Keywords: Polymersome; Polymer Vesicle; Doxorubicin; Combretastatin; Porphyrin; multi-functional; theranostic; Analytical, Diagnostic and Therapeutic Techniques and Equipment; Biomedical Engineering and Bioengineering; Chemical Engineering

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APA (6th Edition):

Levine, D. H. (2010). POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/405

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):

Levine, Dalia H. “POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS.” 2010. Thesis, University of Pennsylvania. Accessed June 17, 2019. https://repository.upenn.edu/edissertations/405.

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

MLA Handbook (7th Edition):

Levine, Dalia H. “POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS.” 2010. Web. 17 Jun 2019.

Vancouver:

Levine DH. POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2019 Jun 17]. Available from: https://repository.upenn.edu/edissertations/405.

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

Council of Science Editors:

Levine DH. POLYMERSOMES: MULTI-FUNCTIONAL TOOLS FOR IN VIVO CANCER THERANOSTIC APPLICATIONS. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/405

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


Université Paris-Sud – Paris XI

12. 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 (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 June 17, 2019. 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. 17 Jun 2019.

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 2019 Jun 17]. 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


Université Paris-Sud – Paris XI

13. Roche, Maxime. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.

Degree: Docteur es, Chimie thérapeutique, 2014, Université Paris-Sud – Paris XI

Les travaux rapportés dans ce mémoire concernent le développement de nouveaux couplages pallado-catalysés de N-tosylhydrazones ainsi que leurs applications à la synthèse d’analogues de l’isocombrétastatine… (more)

Subjects/Keywords: Combrétastatine; Antivasculaire; N-tosylhydrazone; Couplage pallado-catalysé; Réaction tandem; Couplage oxydatif; Combretastatin; Antivascular; N-tosylhydrazone; Palladium catalyzed cross-coupling; Tandem reaction; Oxidative coupling

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APA (6th Edition):

Roche, M. (2014). Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114843

Chicago Manual of Style (16th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed June 17, 2019. http://www.theses.fr/2014PA114843.

MLA Handbook (7th Edition):

Roche, Maxime. “Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4.” 2014. Web. 17 Jun 2019.

Vancouver:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2019 Jun 17]. Available from: http://www.theses.fr/2014PA114843.

Council of Science Editors:

Roche M. Couplages pallado-catalysés de N-tosylhydrazones : synthèse d’oléfines apparentées à l’isocombrétastatine A4 : Palladium catalyzed coupling of N-tosylhydrazones : synthesis of olefines related to isocombretastatin A4. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114843


University of Florida

14. Coomer, Alastair R. A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent.

Degree: MS, Veterinary Medical Sciences - Veterinary Medicine, 2007, University of Florida

 Osteosarcoma (OSA) accounts for up to 98% of all canine primary bone tumors and 5% to 6% of all canine malignancies. Radiation therapy forms an… (more)

Subjects/Keywords: Bones; Canines; Dogs; Dosage; Heterologous transplantation; Irradiation; Necrosis; Osteosarcoma; Radiotherapy; Tumors; bevacizumab, canine, carboplatin, combretastatin, human, intramuscular, murine, osteosarcoma, radiation, xenograft

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APA (6th Edition):

Coomer, A. R. (2007). A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0021812

Chicago Manual of Style (16th Edition):

Coomer, Alastair R. “A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent.” 2007. Masters Thesis, University of Florida. Accessed June 17, 2019. http://ufdc.ufl.edu/UFE0021812.

MLA Handbook (7th Edition):

Coomer, Alastair R. “A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent.” 2007. Web. 17 Jun 2019.

Vancouver:

Coomer AR. A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent. [Internet] [Masters thesis]. University of Florida; 2007. [cited 2019 Jun 17]. Available from: http://ufdc.ufl.edu/UFE0021812.

Council of Science Editors:

Coomer AR. A Murine Xenograft Model of Canine Osteosarcoma Anti-Tumor Effects of an Angiogenesis Inhibitor and Combinations of Radiation, Chemotherapy, and a Vascular Targeting Agent. [Masters Thesis]. University of Florida; 2007. Available from: http://ufdc.ufl.edu/UFE0021812

15. 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 June 17, 2019. 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. 17 Jun 2019.

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 2019 Jun 17]. 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

.