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Showing 1 to 20 of 49 for “"thiazole"”.

  1. Strategies for thiazole/oxazole-modified microcin discovery

    … rapidly growing family of natural products, the thiazole/oxazole-modified microcins (TOMMs), and discuss novel methods used to correlate the gene clusters to natural products from this family of metabolites. In chapter 2, I establish the sequence diversity and structural capability of bacteria …

    uiuc Repository record for Strategies for thiazole/oxazole-modified microcin discovery (opens in a new tab)

  2. Synthesis and biophysical evaluation of thiazole orange derivatives as DNA binding ligands

    … by G-quadruplex binding ligands such as Thiazole orange (TO). Compared with other G-quadruplex binding ligands, TO has an intriguing tunable fluorescence property. Upon binding to DNA, the fluorescence of TO can increase up to 1000-fold, making it an attractive probe for studying …

    u-pacific Repository record for Synthesis and biophysical evaluation of thiazole orange derivatives as DNA binding ligands (opens in a new tab)

  3. Exploring Prokaryotic Thiamin Biosynthesis: Mechanistic Studies On Thiamin Thiazole Synthase And Pyrimidine Synthase

    Thiamin (Vitamin B1) is made from a coupling a thiazole and a pyrimidine unit, which are assembled separately. Studies have shown that the biosyntheses of thiazole and pyrimidine are different in prokaryotes versus eukaryotes. Understanding of thiamin biosynthesis is still incomplete and a lot of …

    cornell Repository record for Exploring Prokaryotic Thiamin Biosynthesis: Mechanistic Studies On Thiamin Thiazole Synthase And Pyrimidine Synthase (opens in a new tab)

  4. Synthesis and biological evaluation of thiazole and metergoline derivatives as antimycobacterial and antiplasmodial agents

    … SAR studies were conducted on the 2-amino-4-aryl thiazole scaffold by synthesizing a series of derivatives with different motifs at the various positions of the scaffold. These derivatives exhibited moderate antiplasmodial activity in the CQS strain of P. falciparum, and good antimycobacterial …

    cape-town Repository record for Synthesis and biological evaluation of thiazole and metergoline derivatives as antimycobacterial and antiplasmodial agents (opens in a new tab)

  5. ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI

    … antibacterial activity of a new series of phenylthiazole antibiotics against a panel of clinically-relevant ‘ESKAPE’ pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species). The lead compound 1 was …

    purdue-thes Repository record for ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI (opens in a new tab)

  6. Design, synthesis and characterization of thiazole-based conjugated polymers and their applications to n-channel organic electronics

    … solar cells. Among many electron-poor units, thiazoles stand out as a promising building block for high performance organic semiconductors. This dissertation discusses the development of thiazole-based π-conjugated semiconducting polymers to enhance the electron field-effect mobilities by …

    gatech Repository record for Design, synthesis and characterization of thiazole-based conjugated polymers and their applications to n-channel organic electronics (opens in a new tab)

  7. Spécificité mutationnelle du 2-formylamino 4-(5-nitro 2 furyl) thiazole dans le gène lacI d'escherichia coli

    Afin de mieux comprendre la spécificité mutationnelle des 5-nitrofuranes, nous avons étudié les mutations induites par le 2-formylamino-4-(5-nitro-2-furyl) thiazol (FANFT), un 5-nitrofurane, dans la région NC+ du gène lacl d’Escherichia coli. Le traitement de la souche TC3960 avec 50 |nM de FANFT …

    moncton Repository record for Spécificité mutationnelle du 2-formylamino 4-(5-nitro 2 furyl) thiazole dans le gène lacI d'escherichia coli (opens in a new tab)

  8. On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides

    Thiazole/oxazole-modified microcins (TOMMs) comprise a family of ribosomally synthesized and post-translationally modified peptides (RiPPs) that all contain thiazole and oxazole heterocycles derived from cysteine, serine, and threonine residues, respectively. The thiazole/oxazole heterocycle is …

    uiuc Repository record for On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides (opens in a new tab)

  9. Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process

    … (COD=1,5- cyclooctadiene), with thiophene, thiazole, 4-methyl thiazole and 5-methyl thiazole yields the C-S addition metallacycles (Me₃P)₃Ir-(CH=CHCH=S)CI (I), \ (Me3P)3Ir-(CH=NCH=CHS)CI (II), (Me3P)3Ir-CCH=NC(CH3)=CHS)CI (III) and (Me3P)3Ir (CH=NCH=C(CH3)S)CI (IV), respectively. These …

    vt Repository record for Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process (opens in a new tab)

  10. Mechanistic aspects of thiamine biosynthesis in escherichia coli

    … required for the biosynthesis of the thiazole moiety is derived from cleavage of the C??C? bond of tyrosine in a reaction catalysed by the radical S-adenosyl-L-methionine (SAM) enzyme, tyrosine lyase (ThiH). The aromatic by-product of this reaction in vivo was unequivocally …

    soton Repository record for Mechanistic aspects of thiamine biosynthesis in escherichia coli (opens in a new tab)

  11. Pharmacophore-directed retrosynthesis (PDR) and Density functional theory studies applied to the potent ion channel inhibitor waixenicin A : synthetic studies toward a more stable salarin C congener, thia-salarin C, through the lens of PDR.

    … that replacing the endocyclic oxazole with a thiazole would reduce the rate of the Wasserman rearrangement, as previously shown in simpler systems, improving the stability while ideally not altering the potent anticancer activity given the minor change in conformation as determined by DFT. …

    baylor Repository record for Pharmacophore-directed retrosynthesis (PDR) and Density functional theory studies applied to the potent ion channel inhibitor waixenicin A : synthetic studies toward a more stable salarin C congener, thia-salarin C, through the lens of PDR. (opens in a new tab)

  12. I. A search for organic compounds as colorimetric quantitative reagents for inorganic ions ; II. A study of the reaction between 2 acetamino 6 amino benzo thiazole and chloroiridic acid

    The reaction between 2 acetamino 6 amino benzo thiazole and chloroiridio acid is not sensitive enough to be of importance as a colorimetric quantitative reaction. IrCl₆-- can be detected with this organic compound if iridium is present in as much as 0.02 mg. per ml. of solution providing ferric …

    vt Repository record for I. A search for organic compounds as colorimetric quantitative reagents for inorganic ions ; II. A study of the reaction between 2 acetamino 6 amino benzo thiazole and chloroiridic acid (opens in a new tab)

  13. Studies of thiamine biosynthesis

    … (Hmp-PP) and 4-methyl-5-(?-hydroxyethyl)thiazole phosphate (Thz-P). The thiazole moiety is biosynthesised from 1-deoxyxylulose-5-phosphate, tyrosine, and cysteine, and at least six genes are required including thiH, thiG, thiS, and thiF. Whilst in aerobes, the C2-N3 fragment of Thz-P …

    soton Repository record for Studies of thiamine biosynthesis (opens in a new tab)

  14. Analysis of the effect of various ligands on the hydrolysis of ruthenium (III) complexes and interpretation of kinetics of hydrolysis profiles by UV-visible spectrophotometry

    … ligands utilized in this project are imidazole, thiazole, and 1H-1,2,4-triazole. Among these, ruthenium imidazole has passed the Phase I clinical trials. For the ruthenium-imidazole (RIM) complex and the ruthenium-thiazole (RTZ) complex, rates of the hydrolysis reaction are determined by fitting …

    emich Repository record for Analysis of the effect of various ligands on the hydrolysis of ruthenium (III) complexes and interpretation of kinetics of hydrolysis profiles by UV-visible spectrophotometry (opens in a new tab)

  15. Reactions of 4-chloro-2,6-dimethoxypyrimidine and 2-chlorothiazole with carbanion nucleophiles

    … Photostimulated reaction of 2-chlorothiazole (2) with the potassium enolate of pinacolone proceeds by a radical-chain mechanism to give the substitution product resulting from chloride displacement. However, when 2 is allowed to react with pinacolone enolate in the dark a completely …

    vt Repository record for Reactions of 4-chloro-2,6-dimethoxypyrimidine and 2-chlorothiazole with carbanion nucleophiles (opens in a new tab)

  16. Metabolic Stability And Pharmacokinetics In Lead Optimization Of Potential Anti-Psychostimulant Pharmacotherapies

    … [3-(4-(4-cyclohexylpiperazin-1-yl)butyl)benzo[d]thiazole-2(3h)-thione] a highly selective sigma receptor antagonist using a validated UPLC/MS method. However due to its poor in vivo and in vitro performance further research was halted. Several analogs were then synthesized by blocking the …

    mississippi Repository record for Metabolic Stability And Pharmacokinetics In Lead Optimization Of Potential Anti-Psychostimulant Pharmacotherapies (opens in a new tab)

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