Synthesis of 2-amino-1,4-dihydro-4-quinolinones and diaminomethylene Meldrum’s acids derivatives as potential potassium channel openers

in Journal of Heterocyclic Chemistry (2002), 39

Synthesis of 2-Diethoxyphosphoryl-2-Methyl-5-Phenyl-3,4-Dihydro-2H-Pyrrole-1-Oxide (DEPMPO-Ph): a New Radical Spin-Trap

in Symposium Drug Discovery Strategies: from Leads to Drugs (2001, November 16)

The synthesis of a new radical spin trap is presented here: the 2-Diethoxyphosphoryl-2-Methyl-5-Phenyl-3,4-Dihydro-2H-Pyrrole-1-Oxide (DEPMPO-Ph)

Synthesis of 75Se-2-phenyl-1,2-benzisoselenazol-3-(2H)-one (PZ 51; EBSELEN*). A novel biologically active organo-selenium compound

in Journal of Labelled Compounds & Radiopharmaceuticals (1986), 23(1), 59-65

The preparation of 75Se-ebselen (75Se-PZ 51) in a high radiochemica] yield (~40 %) and with a specific act'ivity of 240 mCi/mM (8.9 GBq/mM) is described.

Synthesis of [18F]FDG with alkaline hydrolysis on a low polarity solid phase support.

in Journal of Labelled Compounds & Radiopharmaceuticals (1997), 40

Synthesis of [Gamma-32p]Thiamine Triphosphate

in Analytical Biochemistry (1988), 169(2), 274-278

We developed a novel chemical synthesis of thiamine triphosphate which allows us to incorporate 32P in the gamma position. The reaction is based on the condensation of [32P]orthophosphoric acid and ... [more ▼]

We developed a novel chemical synthesis of thiamine triphosphate which allows us to incorporate 32P in the gamma position. The reaction is based on the condensation of [32P]orthophosphoric acid and thiamine diphosphate in the presence of ethyl chloroformate. After purification by two ion-exchange purification steps, the thiamine derivative has a specific radioactivity of 10 Ci/mmol. The average final yield synthesis is about 10%. [less ▲]

Synthesis of a series of 4H-1,2,4-pyridothiadiazine 1,1-dioxides and their evaluation as new potassium channel openers

Conference (1994, March)

Synthesis of a simplified bryostatin C-ring analogue that binds to the CRD2 of human PKC-alpha and construction of a novel BC-analogue by an unusual Julia olefination process

in Organic Letters (2003), 5(4), 499-502

[GRAPHICS] The synthesis of two truncated bryostatin analogues 2 and 3 is described. High-field NMR measurements on the C-ring analogue 3 in (CH3CN)-H-2 containing 25% (H2O)-H-2 have shown that it binds ... [more ▼]

[GRAPHICS] The synthesis of two truncated bryostatin analogues 2 and 3 is described. High-field NMR measurements on the C-ring analogue 3 in (CH3CN)-H-2 containing 25% (H2O)-H-2 have shown that it binds to the CRD2 of human PKC-alpha at virtually the same position as phorbol-13-acetate (PA) and bryostatin 1 (1). NMR titration studies have also revealed that 3 binds to the CRD2 with a potency similar in magnitude to PA but much less potently than 1. [less ▲]

Synthesis of adherent hydrophilic polypyrrole coatings onto (semi)conducting surfaces

in Chemistry of Materials (2007), 19(9), 2364-2371

Hydrophilic and adherent polypyrrole coatings were prepared by a two-step electrochemical method. First, alpha-pyrrole, omega-acrylate polyethylene oxide (Py-PEO-A) dual macromonomer was synthesized by ... [more ▼]

Hydrophilic and adherent polypyrrole coatings were prepared by a two-step electrochemical method. First, alpha-pyrrole, omega-acrylate polyethylene oxide (Py-PEO-A) dual macromonomer was synthesized by anionic polymerization and electrografted onto (semi)conducting substrates by cathodic polymerization of the acrylic end-group. The obtained adherent coating is hydrophilic and thus swells in water and bears a pyrrole ring, a precursor of the conducting polymer. In a second step, the coating is anodically polarized in a mixture of Py and Py-PEO to give the hydrophilic and adherent polypyrrole. Properties such as morphology, adherence, electroactivity, and hydrophilicity of these coatings were investigated by conventional methods and compared to those of pure polypyrrole coatings. These novel coatings exhibit efficient protein adsorption repellency and are thus good candidates for applications in biomaterials and biosensors. [less ▲]

Synthesis of amonabactins by Aeromonas hydrophila : implication of NRPS of a unique iterate-alternative type

Poster (2011)

Synthesis of amphiphilic copolymers of poly(ethylene oxide) and poly(epsilon-caprolactone) with different architectures, and their role in the preparation of stealthy nanoparticles

in Advanced Functional Materials (2006), 16(11), 1506-1514

Well-defined copolymers of biocompatible poly(epsilon-caprolactone) (PCL) and poly(ethylene oxide) (PEO) are synthesized by two methods. Graft copolymers with a gradient structure are prepared by ring ... [more ▼]

Well-defined copolymers of biocompatible poly(epsilon-caprolactone) (PCL) and poly(ethylene oxide) (PEO) are synthesized by two methods. Graft copolymers with a gradient structure are prepared by ring-opening copolymerization of epsilon-caprolactone (FCL) with a PEO macromonomer of the epsilon CL-type. The epsilon CL polymerization is initiated by a PEO macroinitiator to prepare diblock copolymers. These amphiphilic copolymers are used as stabilizers for biodegradable poly(DL-lactide) (PLA) nanoparticles prepared by a nanoprecipitation technique. The effect of the copolymer characteristic features (architecture, composition, and amount) on the nanoparticle formation and structure is investigated. The average size, size distribution, and stability of aqueous suspensions of the nanoparticles is measured by dynamic light scattering. For comparison, an amphiphilic random copolymer, poly(methyl methacrylate-co-methacrylic acid) (P(MMA-co-MA)), is synthesized. The stealthiness of the nanoparticles is analyzed in relation to the copolymer used as stabilizer. For this purpose, the activation of the complement system by nanoparticles is investigated in vitro using human serum. This activation is much less important whenever the nanoparticles are stabilized by a PEO-containing copolymer rather than by the P(MMA-co-MA) amphiphile. The graft copolymers with a gradient structure and the diblock copolymers with similar macromolecular characteristics (molecular weight and hydrophilicity) are compared on the basis of their capacity to coat PLA nanoparticles and to make them stealthy. [less ▲]