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You searched for subject:(Antimalarials Design). Showing records 1 – 5 of 5 total matches.

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Stellenbosch University

1. De Jager, Josephus Jacobus. Design and synthesis of novel antimalarial agents.

Degree: MSc, 2014, Stellenbosch University

ENGLISH ABSTRACT: Malaria is a pestilent disease associated with massive socioeconomic burden of sub-Saharan Africa. This disease is caused by a blood infection of the… (more)

Subjects/Keywords: Industrial psychology; Antimalarials  – Development; Antimalarials  – Design

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APA (6th Edition):

De Jager, J. J. (2014). Design and synthesis of novel antimalarial agents. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/96071

Chicago Manual of Style (16th Edition):

De Jager, Josephus Jacobus. “Design and synthesis of novel antimalarial agents.” 2014. Masters Thesis, Stellenbosch University. Accessed October 18, 2019. http://hdl.handle.net/10019.1/96071.

MLA Handbook (7th Edition):

De Jager, Josephus Jacobus. “Design and synthesis of novel antimalarial agents.” 2014. Web. 18 Oct 2019.

Vancouver:

De Jager JJ. Design and synthesis of novel antimalarial agents. [Internet] [Masters thesis]. Stellenbosch University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10019.1/96071.

Council of Science Editors:

De Jager JJ. Design and synthesis of novel antimalarial agents. [Masters Thesis]. Stellenbosch University; 2014. Available from: http://hdl.handle.net/10019.1/96071


Northeastern University

2. Iyamu, Iredia David. Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents.

Degree: PhD, Department of Chemistry and Chemical Biology, 2016, Northeastern University

 Malaria is a mosquito-borne infectious disease, which remains a public health challenge globally. About half of the world population is at risk with 214 million… (more)

Subjects/Keywords: malaria; spirocyclic chromanes; dihydropyridines; naphthoquinones; Antimalarials; Heterocyclic compounds; Synthesis; Dihydropyridine; Synthesis; Naphthoquinone; Synthesis; Naphthalene; Drugs; Design

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APA (6th Edition):

Iyamu, I. D. (2016). Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20211573

Chicago Manual of Style (16th Edition):

Iyamu, Iredia David. “Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents.” 2016. Doctoral Dissertation, Northeastern University. Accessed October 18, 2019. http://hdl.handle.net/2047/D20211573.

MLA Handbook (7th Edition):

Iyamu, Iredia David. “Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents.” 2016. Web. 18 Oct 2019.

Vancouver:

Iyamu ID. Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2047/D20211573.

Council of Science Editors:

Iyamu ID. Design, synthesis and evaluation of spirocyclic chromanes, dihydropyridines, and naphthoquinones as antimalarial agents. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20211573


Tartu University

3. Viira, Birgit. Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria .

Degree: 2017, Tartu University

 Käesolev uurimus keskendub kahele ohtlikule infektsioonhaigusele: inimese immuunpuudulikkuse viirus tüüp 1 (HIV-1) ja malaaria. Uue ravimi väljatöötamine algusest lõppuni on aega nõudev ning kulukas protsess,… (more)

Subjects/Keywords: malaaria; HIV-1; pöördtranskriptaas; malaariavastased ravimid; immuunsüsteemi mõjustavad ravimid; antiviiruslik aktiivsus; ravimidisain; malaria; reverse transcriptase; antimalarials; immunomodulators; antiviral activity; drug design

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

APA (6th Edition):

Viira, B. (2017). Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/57134

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):

Viira, Birgit. “Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria .” 2017. Thesis, Tartu University. Accessed October 18, 2019. http://hdl.handle.net/10062/57134.

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

MLA Handbook (7th Edition):

Viira, Birgit. “Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria .” 2017. Web. 18 Oct 2019.

Vancouver:

Viira B. Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria . [Internet] [Thesis]. Tartu University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10062/57134.

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

Council of Science Editors:

Viira B. Design and modelling in early drug development in targeting HIV-1 reverse transcriptase and Malaria . [Thesis]. Tartu University; 2017. Available from: http://hdl.handle.net/10062/57134

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


ETH Zürich

4. Zürcher, Martina. Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine.

Degree: 2009, ETH Zürich

Subjects/Keywords: ANTIMALARIA-MITTEL (PHARMAZIE); ENZYMINHIBITOREN (BIOCHEMIE); ORGANISCHE SYNTHESE (CHEMIE); FEINSTRUKTUR VON KRISTALLEN; MOLECULAR MODELING + MOLECULAR DESIGN (CHEMIE); ANTIMALARIALS (PHARMACY); ENZYME INHIBITORS (BIOCHEMISTRY); ORGANIC SYNTHESIS (CHEMISTRY); FINE STRUCTURE OF CRYSTALS; MOLECULAR MODELING + MOLECULAR DESIGN (CHEMISTRY); info:eu-repo/classification/ddc/540; info:eu-repo/classification/ddc/610; Chemistry; Medical sciences, medicine

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

APA (6th Edition):

Zürcher, M. (2009). Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/151492

Chicago Manual of Style (16th Edition):

Zürcher, Martina. “Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine.” 2009. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/151492.

MLA Handbook (7th Edition):

Zürcher, Martina. “Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine.” 2009. Web. 18 Oct 2019.

Vancouver:

Zürcher M. Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine. [Internet] [Doctoral dissertation]. ETH Zürich; 2009. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/151492.

Council of Science Editors:

Zürcher M. Strukturbasiertes Design und Synthese von Inhibitoren der Plasmepsine und Falcipaine. [Doctoral Dissertation]. ETH Zürich; 2009. Available from: http://hdl.handle.net/20.500.11850/151492


ETH Zürich

5. Fäh, Christoph. Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere.

Degree: 2009, ETH Zürich

Subjects/Keywords: CYCLISCHE KETONE (ORGANISCHE CHEMIE); FLUORORGANISCHE VERBINDUNGEN; PROTEASENINHIBITOREN; ASPARTISCHE PROTEINASEN (ENZYME); ANTIMALARIA-MITTEL (PHARMAZIE); ARZNEIMITTELENTWICKLUNG + ARZNEIMITTELDESIGN + ARZNEIMITTELENTDECKUNG; CYCLIC KETONES (ORGANIC CHEMISTRY); FLUORINE-ORGANIC COMPOUNDS; PROTEASE INHIBITORS (BIOCHEMISTRY); ASPARTIC PROTEINASES (ENZYMES); ANTIMALARIALS (PHARMACY); DRUG DEVELOPMENT + DRUG DESIGN + DRUG DISCOVERY (PHARMACY); info:eu-repo/classification/ddc/540; info:eu-repo/classification/ddc/610; Chemistry; Medical sciences, medicine

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

APA (6th Edition):

Fäh, C. (2009). Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/151184

Chicago Manual of Style (16th Edition):

Fäh, Christoph. “Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere.” 2009. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/151184.

MLA Handbook (7th Edition):

Fäh, Christoph. “Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere.” 2009. Web. 18 Oct 2019.

Vancouver:

Fäh C. Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere. [Internet] [Doctoral dissertation]. ETH Zürich; 2009. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/151184.

Council of Science Editors:

Fäh C. Zyklische Difluorketone: neue Bausteine für Inhibitoren der Aspartylproteasen Plasmepsin I-IV und für die Darstellung auf C=O...C=O-Wechselwirkungen basierter Homodimere. [Doctoral Dissertation]. ETH Zürich; 2009. Available from: http://hdl.handle.net/20.500.11850/151184

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