Lição

Comme pour la cérémonie d’ouverture des Jeux Olympiques de Londres le 27 juillet 2012, organisée par le réalisateur de Trainspotting et de Slumdog Millionaire Danny Boyle, qui fit une récapitulation de tous les grands événements qui identifient la Grande-Bretagne et sa population : l’invention de nombreux sports, la révolution industrielle, la reine d’Angleterre et James Bond, l’humour , la littérature , l’inventeur des www (world wide web), l’écographie, les Hôpitaux , les nurses et les nounous , la musique , je me propose de cerner l’identité et l’âme françaises grâce à leurs caractéristiques et à des clichés, complétés par des nouvelles d’actualité, sans pour autant faire un hymne à la France. Notons au passage que la 1ère langue des J.O est le français, en hommage au baron Pierre de Coubertin. L’Article 23 de la Charte du Comité International Olympique a donné au français le status de langue officielle (comme l’anglais) depuis les J.O d’Athènes de 2004. De plus, les sportifs français ont remporté 34 médailles, essentiellement en natation (avec des nageurs qui s’entrainent surtout à Nice et à Marseille), au pistolet, au judo, en saut à la perche, en équitation, en hand-ball, en volley ball féminin, en taekwondo féminin, en cyclisme féminin... ; nous n’avons rien gagné en escrime. Ils ont été encouragés par F. Hollande, par Christine Lagarde, Présidente du FMI, ex-membre de l’équipe de France de natation synchronisée et par la Ministre des sports Valérie Fourneyrou. Nos sportifs et leurs supporteurs sont rentrés en France par l’Eurostar. Pour intéresser la classe, je m’efforce de parler d’événements que nos élèves auront vu à la télé ou sur Internet afin que ceux-ci puissent participer et donner leur point de vue, en les poussant à vérifier leurs informations dans les médias actuels.

Steroselective synthesis of imidazolidin-4-ones from α-amino amides of the antimalarial primaquine and substituted benzaldehydes

Imidazolidin-4-ones are commonly employed as skeletal modifications in bioactive oligopeptides, either as proline surrogates or for protection of the N-terminal amino acid against aminopeptidase-catalysed hydrolysis . We have been working on the synthesis of imidazolidin-4-ones of the antimalarial primaquine , through acylation of primaquine with an α-amino acid and subsequent reaction of the resulting α-aminoamide with a ketone or aldehyde. Thus, when using racemic primaquine, an optically pure chiral α-amino acid and an aldehyde as starting materials, four imidazolidin-4-one diastereomers are to be expected (Scheme 1). However, we have recently observed that imidazolidin-4-one synthesis was stereoselective when 2-carboxybenzaldehyde (2CBA)* was used, as only two diastereomers were produced2. Computational studies have shown that the imine formed prior to ring closure had, for structures derived from 2CBA, a quasi-cyclic rigid structure2. This rigid conformation is stabilized by an intramolecular hydrogen bond involving the C=O oxygen atom of the 2-carboxyl substituent in 2CBA and the N-H group of the α-amino amide moiety2. These findings led us to postulate that the 2-carbonyl substituent in the benzaldehyde moiety was the key for the stereoselective synthesis of the imidazolidin-4-ones2.

Anti-pneumoscystis carinni activitiy of primaquine imidazolidin-4-ones

Pneumocystis pneumonia (PCP) is one of the most frequent causes of mortality among HIV-infected patients. Primaquine (PQ) is an antimalarial 8-aminoquinoline effective against PCP when given in combination with clindamycin. This has drawn the attention of Medicinal Chemists towards the anti-PCP activity of 8-aminoquinolines, not only confined to those exhibiting antimalarial activity [1]. It is thought that anti-PCP 8-aminoquinolines exert their anti-PCP activity by acting on the electronic transport and redox system of the P. carinii pathogen [1]. Recently, our research group has been developing imidazolidin-4-one derivatives of PQ (Scheme 1), targeting novel compounds with improved therapeutic action, namely, higher resistance to metabolic inactivation, lower toxicity and equal or higher antimalarial activity than that of the parent drug [2,3]. These imidazolidin-4-ones were seen to block the transmission of rodent malaria, caused by Plasmodium berghei on BalbC mice, to the mosquito vector Anopheles stephensi [3]. The anti-PCP activity of our PQ derivatives is now under study and preliminary in vitro assays [4] show that some of the compounds exhibit slight to moderate activity after a 72 h incubation period against P. carinii. In one case, the IC50 was comparable to that of parent PQ. Both these studies and forthcoming results from ongoing biological assays will be presented and discussed.

Abordagem tradicional ao cálculo de custos: a necessidade da medida da produção

Neste texto são analisadas técnicas e/ou métodos para calcular custos sustentando a percepção de que as empresas em geral e as pequenas e médias empresas (PME) em particular, necessitam de conhecer os custos dos produtos que fabricam e vendem e/ou dos serviços que prestam...

Development and biological evaluation of API-ILs based on anti-bacterial and anti-fungal drugs

In recent years Ionic Liquids (ILs) are being applied in life sciences. ILs are being produce with active pharmaceutical drugs (API) as they can reduce polymorphism and drug solubility problems [1] Also ILs are being applied as a drug delivery device in innovative therapies What is appealing in ILs is the ILs building up platform, the counter-ion can be carefully chosen in order to avoid undesirable side effects or to give innovative therapies in which two active ions are paired. This work shows ILs based on ampicillin (an anti-bacterial agent) and ILs based on Amphotericin B. Also we show studies that indicate that ILs based on Ampicillin could reverse resistance in some bacteria. The ILs produced in this work were synthetized by the neutralization method described in Ferraz et. al. [2] Ampicillin anion was combined with the following organic cations 1-ethyl-3-methylimidazolium, [EMIM]; 1-hydroxy-ethyl-3-methylimidazolium, [C2OHMIM]; choline, [cholin]; tetraethylammonium, [TEA]; cetylpyridinium, [C16pyr] and trihexyltetradecylphosphonium, [P6,6,6,14]. Amphotericin B was combined with [C16pyr], [cholin] and 1-metohyethyl-3-methylimidazolium, [C3OMIM]. The ILs-APIs based on ampicillin[2] were tested against sensitive Gram-negative bacteria Escherichia coli ATCC 25922 and Klebsiella pneumonia (clinical isolated), as well as on Gram positive Staphylococcus Aureus ATCC 25923, Staphylococcus epidermidis and Enterococcus faecalis. The arising resistance developed by bacteria to antibiotics is a serious public health threat and needs new and urgent measures. We study the bacterial activity of these compounds against a panel of resistant bacteria (clinical isolated strains): E. coli CTX M9, E. coli TEM CTX M9, E. coli TEM1, E. coli CTX M2, E. coli AmpC Mox2. In this work we demonstrate that is possible to produce ILs from anti-bacterial and anti-fungal compounds. We show here that the new ILs can reverse the bacteria resistance. With the careful choice of the organic cation, it is possible to create important biological and physic-chemical properties. This work also shows that the ion-pair is fundamental in ampicillin mechanism of action.

Para a história do ensino contabilistico de Lisboa e do porto no Portugal de oitocentos

Na segunda metade do século XIX foram fundados nas duas maiores cidades do país, Lisboa e Porto, nos anos de 1869 e 1886, respectivamente, dois estabelecimentos de ensino público de contabilidade: o Instituto Comercial de Lisboa e o Instituto Industrial e Comercial do Porto. ...

Projectos de investimento: principais conceitos

Projectos de investimento significa um eventual investimento em activos fixos do qual se espera que remunere quem é proprietário do capital. Para garantir isto aplicam-se vários indicadores que auxilia quem toma decisões económicas e financeiras a granatir a viabilidade do investimento.

As operações com terceiros no direito cooperativo português (comentário ao acórdão do Supremo Tribunal de Justiça de 18 de dezembro de 2007)

Partindo de um Ácrodão do Supremo Tribunal de Justiça que decidiu sobre o destino dos benefícios resultantes nas operações com terceiros nas cooperativas...