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Paclitaxel was isolated from the bark of <i>Taxus brevifolia</i> in the late 1960s. It exerts its biological effect by promoting tubulin polymerization and stabilizing the resulting microtubules. Paclitaxel has become one of the most important current drugs for the treatment of breast and ovarian cancers. Studies aimed at understanding the biologically active conformation of paclitaxel bound on β–tubulin are described. In this work, the synthesis of isotopically labeled taxol analogs is described and the REDOR studies of this compound complexed to tubulin agrees with the hypothesis that palictaxel adopts T-taxol conformation. Based on T-taxol conformation, macrocyclic analogs of taxol have been prepared and their biological activities were evaluated. The results show a direct evidence to support T-taxol conformation. (+) Discodermolide is a polyketide isolated from the Caribbean deep sea sponge <i>Discodermia dissoluta</i> in 1990. Similar to paclitaxel, discodermolide interacts with tubulin and stabilizes the microtubule <i>in vivo</i>. Studies aimed at understanding the biologically active conformation of discodermolide bound on β–tubulin are described. In this work, the synthesis of fluorescent labeled discodermolide analogs is described and their biological activities were evaluated. Synthetic approaches to fluorescent labeled and isotopically labeled discodermolide analogs discodermolide are also described. / Ph. D.

The complex natural product paclitaxel (Taxol®), first isolated from Taxus brevifolia, is a member of a large family of taxane diterpenoids. Paclitaxel is extensively used for the treatment of solid tumors, particularly those of the breasts and ovaries. In order to obtain additional information about the mechanism of action of paclitaxel and the environment of the paclitaxel-binding site, several fluorescent analogs of paclitaxel were synthesized, and their biological activities have been evaluated. For the investigation of possible synergistic effects, concurrent modifications on selected positions have been performed and their biological evaluation were studied. / Ph. D.

The conformation of paclitaxel in the bound state on the protein has been proposed to be the T-taxol conformation, and paclitaxel analogs constrained to the T-taxol conformation proved to be significantly more active than paclitaxel in both cytotoxicity and tubulin polymerization assays, thus validating the T-taxol conformation as the tubulin-binding conformation. In this work, eight compounds containing an aza-tricyclic moiety as a mimic of the baccatin core of paclitaxel have been designed and synthesized as water-soluble simplified paclitaxel analogs, among which 3.50-3.52 and 3.55 were conformationally constrained analogs designed to bind to the paclitaxel binding site of tubulin, based on their similarity to the T-taxol conformation. The open-chain analogs 3.41-3.43 and 3.57 and the bridged analogs 3.50-3.52 and 3.55 were evaluated for their antiproliferative activities against the A2780 cell lines. Analogs 3.50-3.52 and 3.55 which were designed to adopt the T-taxol conformation showed similar antiproliferative activities compared to their open-chain counterparts. They were all much less active than paclitaxel. In the second project, a series of paclitaxel analogs with various thio-containing linkers at C-2′ and C-7 positions were designed and synthesized in our lab. These analogs were attached to the surfaces of gold nanoparticles by CytImmune Sciences for the development of mutifunctional tumor-targeting agents. The native analogs and the gold bound analogs were evaluated for their antiproliferative activities against the A2780 cell line. All the compounds tested showed comparable or better activities than paclitaxel. Stability studies were performed for selected analogs in hydrolysis buffer, which showed that the analogs released paclitaxel in buffer over time. In the third project, the synthesis of a conformationally constrained paclitaxel analog which was designed to mimic the REDOR-taxol conformation was attempted. Two synthetic routes were tried and significant progress was made toward the synthesis of the conformationally constrained analog. However, both of the current synthetic routes failed to produce the key intermediate that would serve as the precursor for a ring-closing metathesis reaction to furnish the macrocyclic ring. / Ph. D.

Yes / 5,7-Dihydro-3,9,10,11-tetramethoxybenz[c,e]oxepin-4-ol 1, prepared from a dibenzyl ether precursor via Pd-catalysed intramolecular direct arylation, possesses broad-spectrum in vitro cytotoxicity towards various tumour cell lines, and induces vascular shutdown, necrosis and growth delay in tumour xenografts in mice at sub-toxic doses. The biological properties of 1 and related compounds can be attributed to their ability to inhibit microtubule assembly at the micromolar level, by binding reversibly to the same site of the tubulin αβ-heterodimer as colchicine 2 and the allocolchinol, N-acetylcolchinol 4.

Paclitaxel is one of the most successful anti-cancer drugs, particularly in the treatment of breast cancer and ovarian cancer. For the investigation of the interaction between paclitaxel and MD-2 protein, and development of new antagonists for lipopolysaccharide, several C10 A-nor-paclitaxel analogs have been synthesized and their biological activities have been evaluated. In order to reduce the myelosuppression effect of the paclitaxel, several C3â ² and C4 paclitaxel analogs have been synthesized and their biological evaluation have been studied. / Master of Science

Die vorliegende Arbeit beinhaltet verschiedene Aspekte der Embryogenese des Pfeilschwanzkrebses Limulus polyphemus (Chelicerata, Xiphosura), darunter die frühe Neurogenese, die Axogenese, eine Analyse der "Kopf"segmentierung bei Cheliceraten und anderen Arthropoden, sowie das Expressionsmuster des Homöoboxgens Distal-less insbesondere in neuronalen Zusammenhängen. Darüber hinaus wurde eine neue Embryonalstadieneinteilung geleistet. Markierungen mit Phalloidin sowie weiterer neurospezifischer Marker ergaben, daß die frühe Neurogenese bei Limulus polyphemus durch die Immigration von Zellclustern erfolgt. Die Zellen nehmen eine flaschenförmige Gestalt annehmen, bevor sie sich aus dem ventralen Neuroektoderm lösen. Die Anzahl der Zellen pro Zellcluster steigt mit fortschreitender Entwicklung. Die Zellcluster konzentrieren sich in in Zentrum jedes Hemisegmentes, und in ihrem dorsalen Bereich beginnt die rasch voranschreitende Axogenese. Die Untersuchung der "Kopf"segmentierung mittels alpha-Tubulin-Markierungen bei Limulus polyphemus, Triops cancriformis (Crustacea) und Lepisma saccharina (Hexapoda) ergab sowohl bei der Entwicklung des circumoesophagealen Neuropilringes und der Innervierung der dazugehörigen Anhangspaare als auch hinsichtlich des Verlaufs des Stomatogastrischen Nervensystems beachtliche Übereinstimmungen, die entgegen der klassischen Auffassung den Schluß zulassen, daß das Deutocerebrum der Cheliceraten keineswegs reduziert wurde oder mit dem Tritocerebrum verschmolzen ist, sondern die Chelicere innerviert. Somit wäre das Chelicerenneuromer homolog zum Deutocerebrum der Crustacea und Hexapoda (1. Antenne). Der Vergleich des Expressionsmuster des Homöoboxgens Distal-less bei Limulus und Lepisma saccharina ergab neben den typischen Expressionen in auswachsenden Extremitäten- und andern Anhangsknospen bei beiden Vertretern Expressionen in neuronalen Zusammenhängen (im Lobus opticus, Ganglien bei Limulus oder in das ZNS umgebende Zellen bei Lepisma), an den verschiedensten Positionen späterer Sinnesorgane wie Mechano- oder Chemorezeptoren. Doppelmarkierungen mit Synorf-1 deuten darauf hin, daß es sich bei den Dll-positiven Zellen zum größten Anteil um Glia-Zellen handelt. / The following study contains different aspects of the embryology of the horseshoe crab Limulus polyphemus (Chelicerata, Xiphosura) with the main focus on early neurogenesis, axogenesis and the "head"segmentation in chelicerates and other arthropods. The expression pattern of the homeobox gene Distal-less was examined with main focus on neuronal correlations. In addition, a new staging was provided. Phalloidin stainings and other markers showed that the early neurogenesis in Limulus polyphemus happens via immigration of cell clusters. Cellclusters in the prosoma contain cells that become bottle shaped before they immigrate from the ventral neuroectoderm. The number of these cells increases during further development, and the cells concentrate in the middle of each hemisegment. Axogenesis starts at the dorsal edge of these concentrated cellclusters and progresses quite fast building the typical ladder like CNS of arthropods. The investigation of the "head"segmentation using alpha-tubulin stainings in Limulus polyphemus, Triops cancriformis (Crustacea), and Lepisma saccharina (Hexapoda) showed remarkable similarities in the development of the circumesophageal neuropil ring, the related appendages, and the course of the stomatogastric nerves. These results lead to the thesis that the deutocerebrum of chelicerates is neither completely reduced nor totally merged into the tritocerebrum but innervates the chelicerae which contradicts the classical view. According to these results the neuromer of the chelicerae would be homologous to the deutocerebrum of Crustaceans and Hexapods (first antennae). The expression pattern of the homeobox gene Distal-less was examined and compared in Limulus polyphemus and Lepisma saccharina. Beside the typical expression pattern in the developing appendages a participation of the gene in development of the nervous system was observed. Dll positve cells were found in or at least in direct contact with the CNS (optical lobe, ganglia in Limulus or surrounding the entire CNS including the brain of Lepisma), at different positions of later mechano- and chemoreceptors (lateral spines, bristles, flabellum, Johnstons organ etc.). Double stainings using Dll and Synorf-1 showed that at least most of these Dll-postive cells are most likely glia cells.