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You searched for subject:(Antimalarials ). Showing records 91 – 113 of 113 total matches.

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University of Pretoria

91. [No author]. The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 .

Degree: 2007, University of Pretoria

Please read the abstract in the section 00front of this document Advisors/Committee Members: Prof C E Medlen (advisor).

Subjects/Keywords: Developing countries; Drug resistance; Antimalarials; Malaria therapy; Malaria prevention; Malaria; UCTD

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APA (6th Edition):

author], [. (2007). The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-01052007-161743/

Chicago Manual of Style (16th Edition):

author], [No. “The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 .” 2007. Doctoral Dissertation, University of Pretoria. Accessed October 18, 2019. http://upetd.up.ac.za/thesis/available/etd-01052007-161743/.

MLA Handbook (7th Edition):

author], [No. “The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 .” 2007. Web. 18 Oct 2019.

Vancouver:

author] [. The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 . [Internet] [Doctoral dissertation]. University of Pretoria; 2007. [cited 2019 Oct 18]. Available from: http://upetd.up.ac.za/thesis/available/etd-01052007-161743/.

Council of Science Editors:

author] [. The antiplasmodial activities of the tetramethylpiperidyl-substituted phenazines, B4119 and B4158 . [Doctoral Dissertation]. University of Pretoria; 2007. Available from: http://upetd.up.ac.za/thesis/available/etd-01052007-161743/


Hong Kong University of Science and Technology

92. Chan, Wing Chi. Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives.

Degree: 2005, Hong Kong University of Science and Technology

 The history and development of the Chinese peroxidic sesquiterpene qinghaosu or artemisinin, and its conversion into the current derivatives artemether and artesunate which are used… (more)

Subjects/Keywords: Artemisia  – Mechanism of action; Artemisia  – Therapeutic use; Antimalarials; Drugs  – Analysis

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APA (6th Edition):

Chan, W. C. (2005). Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b880220 ; http://repository.ust.hk/ir/bitstream/1783.1-4039/1/th_redirect.html

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):

Chan, Wing Chi. “Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives.” 2005. Thesis, Hong Kong University of Science and Technology. Accessed October 18, 2019. https://doi.org/10.14711/thesis-b880220 ; http://repository.ust.hk/ir/bitstream/1783.1-4039/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Chan, Wing Chi. “Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives.” 2005. Web. 18 Oct 2019.

Vancouver:

Chan WC. Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2005. [cited 2019 Oct 18]. Available from: https://doi.org/10.14711/thesis-b880220 ; http://repository.ust.hk/ir/bitstream/1783.1-4039/1/th_redirect.html.

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

Council of Science Editors:

Chan WC. Chemical studies on mechanism of action of the Chinese antimalarial artemisinin and its derivatives. [Thesis]. Hong Kong University of Science and Technology; 2005. Available from: https://doi.org/10.14711/thesis-b880220 ; http://repository.ust.hk/ir/bitstream/1783.1-4039/1/th_redirect.html

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

93. Tesfaselassie, Elias Sibhatu. Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance.

Degree: MS(M.S.) in Chemistry, Chemistry, 2015, Portland State University

  Malaria is considered as one of the most prevalent and debilitating diseases affecting humans. Plasmodium falciparum is the most virulent form of the parasite… (more)

Subjects/Keywords: Triazoles  – Synthesis; Antimalarials  – Synthesis; Chloroquine; Medicinal-Pharmaceutical Chemistry

…discovery .28 2.7. Triazole-based antimalarials ..32 2.8… …triazole-based antimalarials ..39 3.1. First-generation click compounds… …based antimalarials .50 4.1. The first-generation click compounds ...50 4.2… …aminoquinoline antimalarials …..63 5.2. Fluoxetine as reversal agent… …hybrid molecule …...31 Figure 2.6. Triazole-based antimalarials …33… 

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APA (6th Edition):

Tesfaselassie, E. S. (2015). Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance. (Masters Thesis). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/2506

Chicago Manual of Style (16th Edition):

Tesfaselassie, Elias Sibhatu. “Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance.” 2015. Masters Thesis, Portland State University. Accessed October 18, 2019. https://pdxscholar.library.pdx.edu/open_access_etds/2506.

MLA Handbook (7th Edition):

Tesfaselassie, Elias Sibhatu. “Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance.” 2015. Web. 18 Oct 2019.

Vancouver:

Tesfaselassie ES. Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance. [Internet] [Masters thesis]. Portland State University; 2015. [cited 2019 Oct 18]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/2506.

Council of Science Editors:

Tesfaselassie ES. Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance. [Masters Thesis]. Portland State University; 2015. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/2506


University of Cape Town

94. Abrahams, Meryl Arlene. Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum.

Degree: Image, Division of Clinical Pharmacology, 1997, University of Cape Town

 With the increase in recent years in the prevalence of malaria, and in drug resistance of Plasmodium falciparum, there has been much interest in natural… (more)

Subjects/Keywords: Antimalarials; Artemisia - therapeutic use; Malaria - drug therapy; Plasmodium falciparum - drug effects

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APA (6th Edition):

Abrahams, M. A. (1997). Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/26263

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):

Abrahams, Meryl Arlene. “Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum.” 1997. Thesis, University of Cape Town. Accessed October 18, 2019. http://hdl.handle.net/11427/26263.

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

MLA Handbook (7th Edition):

Abrahams, Meryl Arlene. “Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum.” 1997. Web. 18 Oct 2019.

Vancouver:

Abrahams MA. Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum. [Internet] [Thesis]. University of Cape Town; 1997. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11427/26263.

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

Council of Science Editors:

Abrahams MA. Bioassay-guided fractionation of Artemisia afra for in vitro antimalarial activity against Plasmodium falciparum. [Thesis]. University of Cape Town; 1997. Available from: http://hdl.handle.net/11427/26263

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


University of North Carolina – Greensboro

95. McDonald, Molly C. Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase.

Degree: 2009, University of North Carolina – Greensboro

 Orotidine-5'-monophosphate decarboxylase (ODCase) is an enzyme that catalyzes the final step during the de novo synthesis of uridine-5'-monophosphate (UMP). Several UMP derivatives modified at the… (more)

Subjects/Keywords: Enzyme Inhibitors – Research.; Antineoplastic agents – Research.; Antimalarials – Research.; Pyrimidine nucleotides – Metabolism.

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APA (6th Edition):

McDonald, M. C. (2009). Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=2345

Chicago Manual of Style (16th Edition):

McDonald, Molly C. “Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase.” 2009. Masters Thesis, University of North Carolina – Greensboro. Accessed October 18, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=2345.

MLA Handbook (7th Edition):

McDonald, Molly C. “Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase.” 2009. Web. 18 Oct 2019.

Vancouver:

McDonald MC. Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2009. [cited 2019 Oct 18]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=2345.

Council of Science Editors:

McDonald MC. Synthesis of C6-substituted uridine-5'-monophosphate derivatives as potential inhibitors of orotidine-5'-monophosphate decarboxylase. [Masters Thesis]. University of North Carolina – Greensboro; 2009. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=2345


ETH Zürich

96. Anner, Georg. Zur Kenntnis der Chinovasäure.

Degree: 1943, ETH Zürich

Subjects/Keywords: ANTIMALARIA-MITTEL (PHARMAZIE); ANTIMALARIALS (PHARMACY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Anner, G. (1943). Zur Kenntnis der Chinovasäure. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/135256

Chicago Manual of Style (16th Edition):

Anner, Georg. “Zur Kenntnis der Chinovasäure.” 1943. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/135256.

MLA Handbook (7th Edition):

Anner, Georg. “Zur Kenntnis der Chinovasäure.” 1943. Web. 18 Oct 2019.

Vancouver:

Anner G. Zur Kenntnis der Chinovasäure. [Internet] [Doctoral dissertation]. ETH Zürich; 1943. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/135256.

Council of Science Editors:

Anner G. Zur Kenntnis der Chinovasäure. [Doctoral Dissertation]. ETH Zürich; 1943. Available from: http://hdl.handle.net/20.500.11850/135256

97. Menard, Sandie. Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials.

Degree: Docteur es, Microbiologie, 2017, Université Toulouse III – Paul Sabatier

Le paludisme reste l'une des plus redoutables maladies infectieuses avec plus de 200 millions d'infections et près de 430 000 décès chaque année, principalement des… (more)

Subjects/Keywords: Plasmodium falciparum; Cameroun; Résistance; Antipaludiques; Artémisinine; Marqueurs moléculaires; Transmission; Moustique; Anopheles; Plasmodium falciparum; Cameroon; Resistance; Antimalarials; Artemisinin; Molecular markers; Transmission; Mosquito; Anopheles

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APA (6th Edition):

Menard, S. (2017). Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2017TOU30116

Chicago Manual of Style (16th Edition):

Menard, Sandie. “Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials.” 2017. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed October 18, 2019. http://www.theses.fr/2017TOU30116.

MLA Handbook (7th Edition):

Menard, Sandie. “Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials.” 2017. Web. 18 Oct 2019.

Vancouver:

Menard S. Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2017. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2017TOU30116.

Council of Science Editors:

Menard S. Plasmodium falciparum et résistance aux antipaludiques : aperçu et conséquences des facteurs impliqués dans la sélection et la diffusion des parasites résistants : Plasmodium falciparum and resistance to antimalarials. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2017. Available from: http://www.theses.fr/2017TOU30116

98. Wattanavijitkul, Thitima. Population pharmacokinetics of pyronaridine in the treatment of malaria.

Degree: PhD, Pharmacy, 2010, University of Iowa

  A novel pyronaridine-artesunate (PA) combination is being developed as a 3:1 fixed ratio oral combination against P. falciparum and P. vivax malaria. Pyronaridine (PYR)… (more)

Subjects/Keywords: Antimalarials; Pharmacokinetics; Population Pharmacokinetics; Pyramax; Pyronaridine; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Wattanavijitkul, T. (2010). Population pharmacokinetics of pyronaridine in the treatment of malaria. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/622

Chicago Manual of Style (16th Edition):

Wattanavijitkul, Thitima. “Population pharmacokinetics of pyronaridine in the treatment of malaria.” 2010. Doctoral Dissertation, University of Iowa. Accessed October 18, 2019. https://ir.uiowa.edu/etd/622.

MLA Handbook (7th Edition):

Wattanavijitkul, Thitima. “Population pharmacokinetics of pyronaridine in the treatment of malaria.” 2010. Web. 18 Oct 2019.

Vancouver:

Wattanavijitkul T. Population pharmacokinetics of pyronaridine in the treatment of malaria. [Internet] [Doctoral dissertation]. University of Iowa; 2010. [cited 2019 Oct 18]. Available from: https://ir.uiowa.edu/etd/622.

Council of Science Editors:

Wattanavijitkul T. Population pharmacokinetics of pyronaridine in the treatment of malaria. [Doctoral Dissertation]. University of Iowa; 2010. Available from: https://ir.uiowa.edu/etd/622


Indian Institute of Science

99. Pavithra, S. Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum.

Degree: 2006, Indian Institute of Science

 Molecular chaperones have emerged in recent years as major players in many aspects of cell biology. Molecular chaperones are also known as heat shock proteins… (more)

Subjects/Keywords: Plasmodium Falciparum - Protein; Protein Structure; Heat Shock Protein 90; Cellular Organism; Molecular Chaperones; Malarial Parasite - Chaperone Networks; Parasite Development - Plasmodium Falciparum Heat Shock Proteins; Hsp90; Chaperone; Antimalarials; Malaria; Geldanamycin (GA); Biochemistry

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APA (6th Edition):

Pavithra, S. (2006). Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/433

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):

Pavithra, S. “Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum.” 2006. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://hdl.handle.net/2005/433.

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

MLA Handbook (7th Edition):

Pavithra, S. “Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum.” 2006. Web. 18 Oct 2019.

Vancouver:

Pavithra S. Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum. [Internet] [Thesis]. Indian Institute of Science; 2006. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2005/433.

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

Council of Science Editors:

Pavithra S. Functional Role Of Heat Shock Protein 90 From Plasmodium Falciparum. [Thesis]. Indian Institute of Science; 2006. Available from: http://hdl.handle.net/2005/433

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


Indian Institute of Science

100. Kumar, Gyanendra. Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery.

Degree: 2007, Indian Institute of Science

 Malaria, caused by the parasite Plasmodium, continues to exact high global morbidity and mortality rate next only to tuberculosis. It causes 300-500 million clinical infections… (more)

Subjects/Keywords: Anti-Malarial Drugs; Anti-Bacterial Drugs; Fatty Acids - Biosynthesis; Malaria - Drugs; Bacteria - Drugs; Plasmodium Falciparum; Groundnuts - Vitamin B1; Enoyl ACP Reductase; Malaria Parasite; Antimalarials; Malaria Vaccine; FabZ; Enoyl Acyl Carrier Protein Reductase (ENR); PfFabZ; Biochemistry

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APA (6th Edition):

Kumar, G. (2007). Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/589

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):

Kumar, Gyanendra. “Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery.” 2007. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://hdl.handle.net/2005/589.

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

MLA Handbook (7th Edition):

Kumar, Gyanendra. “Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery.” 2007. Web. 18 Oct 2019.

Vancouver:

Kumar G. Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery. [Internet] [Thesis]. Indian Institute of Science; 2007. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2005/589.

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

Council of Science Editors:

Kumar G. Computational And Biochemical Studies On The Enzymes Of Type II Fatty Acid Biosynthesis Pathway : Towards Antimalarial And Antibacterial Drug Discovery. [Thesis]. Indian Institute of Science; 2007. Available from: http://hdl.handle.net/2005/589

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

101. Key, Rebecca E. Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 Callophycolide A is a meroditerpene isolated from Callophycus serratus, a Fijian red macroalgae. Callophycolide A has been shown to inhibit bacterial growth, and it exhibits… (more)

Subjects/Keywords: Callophycus serratus; Hydrolytic kinetic resolution (HKR); Total synthesis; Antimalarials; Natural products

…Mode of action of quinoline-containing antimalarials . . . . . 6 1.3.3 Artemisinin… …intraerythrotic infection stage [19]. The oldest group of antimalarials contain a quinoline… …the antimalarials derived from quinoline offer advantages and disadvantages, which are due… …antimalarials As mentioned previously, quinoline-containing antimalarials are solely active against… …it is logical that the mode of action (MOA) for antimalarials is to interrupt… 

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APA (6th Edition):

Key, R. E. (2015). Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53976

Chicago Manual of Style (16th Edition):

Key, Rebecca E. “Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus.” 2015. Doctoral Dissertation, Georgia Tech. Accessed October 18, 2019. http://hdl.handle.net/1853/53976.

MLA Handbook (7th Edition):

Key, Rebecca E. “Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus.” 2015. Web. 18 Oct 2019.

Vancouver:

Key RE. Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1853/53976.

Council of Science Editors:

Key RE. Progress toward the synthesis of a family of antimalarial diterpenes: potential utilization of Co-salen-catalyzed hydrolytic kinetic resolution (HKR) to form chiral intermediates in the metabolites of Callophycus serratus. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53976

102. Liebman, Katherine May. New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments.

Degree: PhD, Chemistry, 2014, Portland State University

  Intermittent fevers caused by Plasmodium parasites have been known for millennia, and have caused untold human suffering. Today, millions of people are afflicted by… (more)

Subjects/Keywords: Quinoline; Chloroquine; Plasmodium falciparum; Antimalarials  – Therapeutic use  – History; Medicinal-Pharmaceutical Chemistry

…1 1.2: The early history of quinoline antimalarials: How chloroquine came to be… …7 Figure 4: Synthetic antimalarials from the Bayer research team at Elberfeld… …2013). 1.2: The early history of quinoline antimalarials: How chloroquine came to be… …x28;Akoachere, 2005; Meissner, 2006). The first useful synthetic antimalarials… …Synthetic antimalarials from the Bayer research team at Elberfeld. Figure 4: Synthetic… 

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APA (6th Edition):

Liebman, K. M. (2014). New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments. (Doctoral Dissertation). Portland State University. Retrieved from http://pdxscholar.library.pdx.edu/open_access_etds/2114

Chicago Manual of Style (16th Edition):

Liebman, Katherine May. “New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments.” 2014. Doctoral Dissertation, Portland State University. Accessed October 18, 2019. http://pdxscholar.library.pdx.edu/open_access_etds/2114.

MLA Handbook (7th Edition):

Liebman, Katherine May. “New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments.” 2014. Web. 18 Oct 2019.

Vancouver:

Liebman KM. New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments. [Internet] [Doctoral dissertation]. Portland State University; 2014. [cited 2019 Oct 18]. Available from: http://pdxscholar.library.pdx.edu/open_access_etds/2114.

Council of Science Editors:

Liebman KM. New 4-Aminoquinoline Compounds to Reverse Drug Resistance in <i>P. falciparum</i> Malaria, and a Survey of Early European Antimalarial Treatments. [Doctoral Dissertation]. Portland State University; 2014. Available from: http://pdxscholar.library.pdx.edu/open_access_etds/2114


Indian Institute of Science

103. Dende, Chaitanya. Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model.

Degree: 2015, Indian Institute of Science

 Malaria accounts for 198 million cases worldwide; with a high mortality rate. 584000 deaths were reported in 2013. Malaria is a re-emerging disease globally due… (more)

Subjects/Keywords: Antimalarials; Curcumin Adjunct Therapy; Curcumin-Arteether Combination Therapy; Murine Models; Arether-Curcumin Combination Therapy; Cerebral Malarial; Nanocurcumin; Curcumin Antimalarial; Malaria; Curcumin-Artemisinin Combination Therapy; Cucurmin Therapy; PLGA Nanocurcumin; Curcumin-arteether; Areether-curcumin; Biochemistry

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APA (6th Edition):

Dende, C. (2015). Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3553 ; http://etd.iisc.ernet.in/abstracts/4421/G27331-Abs.pdf

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):

Dende, Chaitanya. “Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model.” 2015. Thesis, Indian Institute of Science. Accessed October 18, 2019. http://etd.iisc.ernet.in/2005/3553 ; http://etd.iisc.ernet.in/abstracts/4421/G27331-Abs.pdf.

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

MLA Handbook (7th Edition):

Dende, Chaitanya. “Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model.” 2015. Web. 18 Oct 2019.

Vancouver:

Dende C. Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model. [Internet] [Thesis]. Indian Institute of Science; 2015. [cited 2019 Oct 18]. Available from: http://etd.iisc.ernet.in/2005/3553 ; http://etd.iisc.ernet.in/abstracts/4421/G27331-Abs.pdf.

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

Council of Science Editors:

Dende C. Adjunct Therapy with Curcumin for the Treatment of Malaria : Studies in a Murine Model. [Thesis]. Indian Institute of Science; 2015. Available from: http://etd.iisc.ernet.in/2005/3553 ; http://etd.iisc.ernet.in/abstracts/4421/G27331-Abs.pdf

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

104. Cobb, Ryan E. Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs.

Degree: MS, 0300, 2011, University of Illinois – Urbana-Champaign

 Malaria represents one of the most significant threats to global health today, with half of the world???s population currently at risk. Although there exist several… (more)

Subjects/Keywords: FR-900098; antimalarials; N-acetyltransferase; FrbF; deoxyxylulose-5-phosphate reductoisomerase (Dxr)

…research group first identified the two compounds as potential antimalarials [48]. In… …fosmidomycin and FR-900098 as potent antimalarials and subsequent clinical trials, interest in… …further illustrating the promise of reverse analogs as more potent antimalarials [69]… …even more potent antimalarials. With the recent elucidation and heterologous expression of… …x28;FR900098) as antimalarials. Journal of medicinal chemistry 2010, 53, 5342-5346… 

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APA (6th Edition):

Cobb, R. E. (2011). Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26343

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):

Cobb, Ryan E. “Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed October 18, 2019. http://hdl.handle.net/2142/26343.

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

MLA Handbook (7th Edition):

Cobb, Ryan E. “Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs.” 2011. Web. 18 Oct 2019.

Vancouver:

Cobb RE. Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2142/26343.

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

Council of Science Editors:

Cobb RE. Toward the synthesis and evaluation of novel N-acylated FR-900098 analogs. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26343

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


ETH Zürich

105. Marxer, Adrian. Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure.

Degree: 1940, ETH Zürich

Subjects/Keywords: ANTIMALARIA-MITTEL (PHARMAZIE); HUSTENMITTEL + NIESMITTEL (PHARMAZIE); FABALES (BOTANIK); ANTIMALARIALS (PHARMACY); ANTITUSSIVES + STERNUTATORIES (PHARMACY); FABALES (BOTANY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Marxer, A. (1940). Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/135322

Chicago Manual of Style (16th Edition):

Marxer, Adrian. “Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure.” 1940. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/135322.

MLA Handbook (7th Edition):

Marxer, Adrian. “Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure.” 1940. Web. 18 Oct 2019.

Vancouver:

Marxer A. Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure. [Internet] [Doctoral dissertation]. ETH Zürich; 1940. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/135322.

Council of Science Editors:

Marxer A. Zur Kenntnis der Glycyrrhetinsäure, des Hederagenins und der Chinovasäure. [Doctoral Dissertation]. ETH Zürich; 1940. Available from: http://hdl.handle.net/20.500.11850/135322


University of Florida

106. Van Essen, Frank William, 1947- ( Dissertant ). Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes.

Degree: 1975, University of Florida

Nosema algerae Vavra and Undeen , a microsporidian

Subjects/Keywords: Body tissues; Infections; Insects; Larvae; Microsporidia; Muscle tissues; Nosema; Parasites; Predators; Species; Antimalarials; Entomology and Nematology thesis Ph. D; Nosema  – Disease and pest resistance

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APA (6th Edition):

Van Essen, Frank William, 1. (. D. ). (1975). Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UF00098163

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):

Van Essen, Frank William, 1947- ( Dissertant ). “Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes.” 1975. Thesis, University of Florida. Accessed October 18, 2019. http://ufdc.ufl.edu/UF00098163.

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

MLA Handbook (7th Edition):

Van Essen, Frank William, 1947- ( Dissertant ). “Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes.” 1975. Web. 18 Oct 2019.

Vancouver:

Van Essen, Frank William 1(D). Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes. [Internet] [Thesis]. University of Florida; 1975. [cited 2019 Oct 18]. Available from: http://ufdc.ufl.edu/UF00098163.

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

Council of Science Editors:

Van Essen, Frank William 1(D). Susceptibility of non-target organisms to Nosema algerae Vavra and Undeen, a microsporidian parasite of mosquitoes. [Thesis]. University of Florida; 1975. Available from: http://ufdc.ufl.edu/UF00098163

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


University of Gothenburg / Göteborgs Universitet

107. Tärning, Joel. Piperaquine - Bioanalys, drug metabolism and pharmacokinetics.

Degree: 2007, University of Gothenburg / Göteborgs Universitet

 Malaria is one of the most abundant parasitic diseases in the world affecting many of the poorest economies. The estimated prevalence is 300 to 700… (more)

Subjects/Keywords: Piperaquine; malaria; Plasmodium falciparum; antimalarials; ACT; pharmacokinetics; NONMEM; population pharmacokinetics; NCA; bioavailability; enterohepatic circulation; metabolism; metabolites; animal models; bioanalysis; regression models; validation; HPLC; LC-MS/MS; H-NMR; FTICR-MS

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APA (6th Edition):

Tärning, J. (2007). Piperaquine - Bioanalys, drug metabolism and pharmacokinetics. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/7196

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):

Tärning, Joel. “Piperaquine - Bioanalys, drug metabolism and pharmacokinetics.” 2007. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 18, 2019. http://hdl.handle.net/2077/7196.

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

MLA Handbook (7th Edition):

Tärning, Joel. “Piperaquine - Bioanalys, drug metabolism and pharmacokinetics.” 2007. Web. 18 Oct 2019.

Vancouver:

Tärning J. Piperaquine - Bioanalys, drug metabolism and pharmacokinetics. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2007. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2077/7196.

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

Council of Science Editors:

Tärning J. Piperaquine - Bioanalys, drug metabolism and pharmacokinetics. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2007. Available from: http://hdl.handle.net/2077/7196

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

108. Nyadong, Leonard. Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates.

Degree: PhD, Chemistry and Biochemistry, 2009, Georgia Tech

 Ambient mass spectrometry (MS) is a new and growing sub-field in MS which has opened new research avenues, particularly for applications relating to the analysis… (more)

Subjects/Keywords: Direct analysis in real time; Counterfeit drugs; Antimalarials; Artemisinins; Desorption electrospray ionization; Ambient mass spectrometry; Mass spectrometry; Mass spectrometry Forensic applications; Chemistry, Forensic

ANTIMALARIALS VIA NONCOVALENT COMPLEX FORMATION… …67 CHAPTER 4. DIRECT QUANTITATION OF ACTIVE INGREDIENTS IN SOLID ARTESUNATE ANTIMALARIALS… …CHARACTERIZING COUNTERFEIT ARTEMISININ-BASED ANTIMALARIALS ............................178 APPENDIX A… …61 xvi Figure 3.5. Reactive DESI spectra of artemisinin-based antimalarials tablets… 

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APA (6th Edition):

Nyadong, L. (2009). Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31694

Chicago Manual of Style (16th Edition):

Nyadong, Leonard. “Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates.” 2009. Doctoral Dissertation, Georgia Tech. Accessed October 18, 2019. http://hdl.handle.net/1853/31694.

MLA Handbook (7th Edition):

Nyadong, Leonard. “Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates.” 2009. Web. 18 Oct 2019.

Vancouver:

Nyadong L. Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1853/31694.

Council of Science Editors:

Nyadong L. Ambient ionization mass spectrometry for the forensic screening of pharmaceuticals and the determination of potential drug candidates. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/31694


ETH Zürich

109. Baumgartner, Corinne. Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe.

Degree: 2007, ETH Zürich

Subjects/Keywords: ANTIMALARIA-MITTEL (PHARMAZIE); SYNTHASEN (ENZYME); PROTEINE, POLYPEPTIDE, ENZYME, ENZYMINHIBITOREN, PEPTIDE (PHARMAZIE); ANTIMALARIALS (PHARMACY); SYNTHASES (ENZYMES); PROTEINS, POLYPEPTIDES, ENZYMES, ENZYME INHIBITORS, PEPTIDES (PHARMACY); info:eu-repo/classification/ddc/610; Medical sciences, medicine

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APA (6th Edition):

Baumgartner, C. (2007). Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/150102

Chicago Manual of Style (16th Edition):

Baumgartner, Corinne. “Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe.” 2007. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/150102.

MLA Handbook (7th Edition):

Baumgartner, Corinne. “Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe.” 2007. Web. 18 Oct 2019.

Vancouver:

Baumgartner C. Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe. [Internet] [Doctoral dissertation]. ETH Zürich; 2007. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/150102.

Council of Science Editors:

Baumgartner C. Strukturbasiertes Design und Synthese von Inhibitoren des Enzyms IspF als potentielle Antimalaria-Wirkstoffe. [Doctoral Dissertation]. ETH Zürich; 2007. Available from: http://hdl.handle.net/20.500.11850/150102


ETH Zürich

110. Tonazzi, Sandro. Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren.

Degree: 2014, ETH Zürich

Subjects/Keywords: ARZNEIMITTELSYNTHESE; HARNDESINFEKTIONSMITTEL + HARNWEGDESINFEKTIONSMITTEL (PHARMAZIE); ENZYMINHIBITOREN (BIOCHEMIE); ANTIMALARIA-MITTEL (PHARMAZIE); SYNTHESIS OF PHARMACEUTICAL DRUGS; URINARY ANTISEPTICS (PHARMACY); ENZYME INHIBITORS (BIOCHEMISTRY); ANTIMALARIALS (PHARMACY); info:eu-repo/classification/ddc/540; info:eu-repo/classification/ddc/610; Chemistry; Medical sciences, medicine

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APA (6th Edition):

Tonazzi, S. (2014). Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154644

Chicago Manual of Style (16th Edition):

Tonazzi, Sandro. “Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren.” 2014. Doctoral Dissertation, ETH Zürich. Accessed October 18, 2019. http://hdl.handle.net/20.500.11850/154644.

MLA Handbook (7th Edition):

Tonazzi, Sandro. “Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren.” 2014. Web. 18 Oct 2019.

Vancouver:

Tonazzi S. Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/20.500.11850/154644.

Council of Science Editors:

Tonazzi S. Strukturbasiertes Design und Synthese von Arylsulfat-Sulfotransferase- (ASST) und Serin-Hydroxymethyltransferase- (SHMT) Inhibitoren. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/154644

111. Didaskalou, Athanasios. Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών.

Degree: 2013, Democritus University of Thrace (DUTH); Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ)

Drug eruptions are a specific body reaction to drugs with manifestations in the skin and mucosae. These are characterized by many different lesions as they… (more)

Subjects/Keywords: Σταθερό φαρμακευτικό εξάνθημα; Ιλαροειδές εξάνθημα; Κνιδωτικό εξάνθημα; Λειχηνοειδές εξάνθημα; Φυσσαλιδώδες εξάνθημα; Φωτοδερματοπάθειες; Αλλεργική αγγειίτιδα; Δισκοειδής ερυθυματώδης λύκος; Πολύμορφο ερύθημα; Οζώδες ερύθημα; Τοξική επιδερμιδική νεκρόλυση; Πέμφιγα; Ερπητοειδής δερματίτιδα; Καλόηθες λεμφοκυττάρωμα του δέρματος; Αλογονοδερματοπάθειες; Αργυρίαση; Αρσενική κερατίαση; Αντιβιοτικά; Ιστολογικές αλλοιώσεις; Αιτιοπαθογένεια; Φάρμακα; Ηλεκτρονικό μικροσκόπιο; Ιστοπαθολογική μελέτη; Fixed drug eruption; Morbilliform eruption; Urticarial allergic eruption; Lichenoid; Vesicular eruption; Photodermatitis; Allergic vasculitis; Discoid lupus erythematosus; Erythema multiforme; Erythema nodosum; Toxic epidermal necrolysis; Benign lymphocytoma cutis; Halogenodermas; Argyria; Arsenic keratosis; Drug eruptions; Antibiotics; NSAID; Analgesis; Drugs; Diuretics; Tranquilizers; Antihypertansive's; Antimalarials; Antidiabetics; Laxatives; Anticoagulants; Anesthetics; Halogens; Anti-thyroid drugs; Contraceptives; Anti TB drugs; Histologic patterns

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APA (6th Edition):

Didaskalou, A. (2013). Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών. (Thesis). Democritus University of Thrace (DUTH); Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/34875

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):

Didaskalou, Athanasios. “Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών.” 2013. Thesis, Democritus University of Thrace (DUTH); Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ). Accessed October 18, 2019. http://hdl.handle.net/10442/hedi/34875.

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

MLA Handbook (7th Edition):

Didaskalou, Athanasios. “Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών.” 2013. Web. 18 Oct 2019.

Vancouver:

Didaskalou A. Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών. [Internet] [Thesis]. Democritus University of Thrace (DUTH); Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ); 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10442/hedi/34875.

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

Council of Science Editors:

Didaskalou A. Κωδικοποίηση των ευρημάτων της κλινικής και ιστοπαθολογικής μελέτης των φαρμακευτικών εξανθημάτων και ενανθημάτων σε σχέση με την αιτιοπαθογένεια και την πρόγνωση αυτών. [Thesis]. Democritus University of Thrace (DUTH); Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ); 2013. Available from: http://hdl.handle.net/10442/hedi/34875

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


ETH Zürich

112. 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 (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


ETH Zürich

113. 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

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