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1.
Eur J Med Chem ; 43(6): 1270-5, 2008 Jun.
Article in English | MEDLINE | ID: mdl-17854952

ABSTRACT

New hexahydropyrimido[5,4-c]quinoline-2,5-diones and 2-thioxohexahydropyrimido[5,4-c]quinoline-5-ones were prepared in two steps from ethyl 4-phenyl-6-methyl-2-oxo tetrahydropyrimidine-5-carboxylates or 4-phenyl-6-methyl-2-thioxotetrahydropyrimidine-5-carboxylates, previously prepared by Biginelli reaction using appropriate aldehyde, urea derivatives and ethyl acetoacetate. Their antioxidant properties were evaluated by two methods: scavenging effect on 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals and scavenging effect on hydroxyl radicals. The results show that the compounds containing thiourea moiety have better activity.


Subject(s)
Antioxidants/chemical synthesis , Antioxidants/pharmacology , Quinolones/chemical synthesis , Quinolones/pharmacology , Free Radical Scavengers/chemical synthesis , Free Radical Scavengers/pharmacology , Hydroxyl Radical/chemistry , Magnetic Resonance Spectroscopy , Spectrophotometry, Infrared
2.
J Chromatogr B Analyt Technol Biomed Life Sci ; 856(1-2): 113-20, 2007 Sep 01.
Article in English | MEDLINE | ID: mdl-17588506

ABSTRACT

A biochromatographic approach is developed to measure for the first time changes in enthalpy, heat capacity change and protonation for the binding of nor-NOHA to arginase in a wide temperature range. For this, the arginase enzyme was immobilized on a chromatographic support. It was established that this novel arginase column was stable during an extended period of time. The affinity of nor-NOHA to arginase is high and changes slightly with the pH, because the number of protons linked to binding is low. The determination of the enthalpy change at different pH values suggested that the protonated group in the nor-NOHA-arginase complex exhibits a heat protonation of approximately -33 kJ/mol. This value agrees with the protonation of an imidazole group. Our result confirmed that active-site residue Hist 141 is protonated as imidazolium cation. Hist 141 can function as a general acid to protonate the leaving amino group of L-ornithine during catalysis. The thermodynamic data showed that nor-NOHA-arginase binding, for low temperature (<15 degrees C), is enthalpically unfavourable and being dominated by a positive entropy change. This result suggests that dehydration at the binding interface and charge-charge interactions contribute to the nor-NOHA-arginase complex formation. The temperature dependence of the free energy of binding is weak because of the enthalpy-entropy compensation caused by a large heat capacity change, DeltaC(p)=-2.43 kJ/mol/K, of arginase. Above 15 degrees C, the thermodynamic data DeltaH and DeltaS became negative due to van der Waals interactions and hydrogen bonding which are engaged at the complex interface confirming strong enzyme-inhibitor hydrogen bond networks. As well, by the use of these thermodynamic data and known correlations it was clearly demonstrated that the binding of nor-NOHA to arginase produces slight conformational changes in the vicinity of the active site. Our work indicated that our biochromatographic approach could soon become very attractive for studying other enzyme-ligand binding.


Subject(s)
Arginase/metabolism , Arginine/analogs & derivatives , Enzymes, Immobilized/metabolism , Histidine/metabolism , Arginine/metabolism , Catalysis , Hydrogen Bonding , Hydrogen-Ion Concentration , Protein Binding , Thermodynamics
3.
Bioorg Med Chem ; 15(6): 2269-82, 2007 Mar 15.
Article in English | MEDLINE | ID: mdl-17275315

ABSTRACT

A number of coumarins exhibit interesting pharmacological activities and are therefore of therapeutic use. We report here the synthesis and the structural analysis of new N-substituted 4-amino-3-(2-methylbenzyl)coumarins (compounds 8a-8e) that present structural analogies with estrothiazine and 11- or 7-substituted 17beta-estradiol. These derivatives were tested with respect to estrogenic activity on the estrogen receptor positive (ER+) human MCF-7 breast cancer cell line. Two of the reported compounds (8a and 8b) stimulated specifically the proliferation of MCF-7 cells, but not that of estrogen receptor negative (ER-) human MDA-MB-231 breast cancer cells, suggesting that their mitogenic activity is mediated by ER. Accordingly, the stimulating effect of 8a and 8b was suppressed by the pure antiestrogen fulvestrant. Besides, 8a and 8b induced ER down-regulation similar to that produced by classical ER agonists or pure antagonists. The effects of the compounds under study on ER-mediated transcription were assessed on (ER+) MVLN cells, that is, MCF-7 cells stably transfected with a pVit-tk-Luc reporter plasmid. Derivatives 8a and 8b, and surprisingly compound 8c, enhanced ER-mediated gene transactivation in that model. Finally, no coumarin was able to compete with tritiated 17beta-estradiol ([(3)H]E(2)) for ER binding, suggesting unconventional interactions with the receptor, such as interactions with the second binding pocket or with the coactivator-binding region. To conclude, observations performed in this study on compound 8c reveal that estrogenic activity can be dissociated from enhancement of cell proliferation. Furthermore, ERE-driven transactivation of transcription seems to be a condition necessary, but not sufficient, for estrogen-induced stimulation of cell growth.


Subject(s)
Antineoplastic Agents/pharmacology , Breast Neoplasms/pathology , Coumarins/chemical synthesis , Estrogens/pharmacology , Cell Proliferation/drug effects , Coumarins/chemistry , Coumarins/pharmacology , Humans , Ligands , Luciferases/metabolism , Models, Molecular , Molecular Structure , Promoter Regions, Genetic , Receptors, Estrogen/genetics , Receptors, Estrogen/metabolism , Thymidine Kinase/genetics , Thymidine Kinase/metabolism , Transcription, Genetic , Transcriptional Activation/drug effects , Tumor Cells, Cultured/drug effects
4.
Electrophoresis ; 26(17): 3247-55, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16143977

ABSTRACT

Novel features of DNA structure, recognition and discrimination have been recently elucidated through the solution structural characterization of DNA aptamers that bind cofactors, amino acids and peptides with high affinity and specificity. Multidimensional nuclear magnetic resonance methodologies have been successfully applied to solve the solution structures. In this work, it was demonstrated that capillary electrophoresis was a powerful tool allowing the fundamental study of the binding mechanism between a DNA aptamer and three ligands, adenosine and adenylate compounds, i.e., adenosine diphosphate (ADP) and adenosine triphosphate (ATP). In order to gain further insight into this binding, thermodynamic measurements under different values of parameters (such as salt nature and its concentration (x) in the run buffer) were carried out. The results showed that dehydration at the binding interface, van der Waals interactions, H-bonding and adjustment of the aptamer recognition surface were implied in the aptamer-ligand association. As well, it was demonstrated that the addition in the medium of the sodium monovalent cation Na(+) or the nickel divalent cation Ni(2+) decreased the complex formation. Separation efficiency and peak shape can also be improved by Mg(2+) divalent cation, which increased the mass transfer kinetics during the ligand-aptamer binding process. A significant separation for the worst separated pair of peaks on the electropherogram ((ADP, ATP) peak pair) was thus achieved.


Subject(s)
Adenosine Diphosphate/metabolism , Adenosine Triphosphate/metabolism , Cations/chemistry , Electrophoresis, Capillary/methods , Oligonucleotides/metabolism , Base Sequence , Hydrogen Bonding , Oligonucleotides/isolation & purification , Thermodynamics
5.
Talanta ; 65(3): 814-8, 2005 Feb 15.
Article in English | MEDLINE | ID: mdl-18969873

ABSTRACT

In a previous manuscript [C. Andre, A. Berthelot, J.F. Robert, M. Thomassin, Y.C. Guillaume, J. Pharm. Bio. Med., in press], the Mg(2+) effect on the testosterone displacement equilibrium from its human serum albumin (HSA) binding site by DHEA was investigated using a thermodynamic approach. In this paper, a novel concept based on the competitive Langmuir distribution isotherms was proposed to calculate the association constant of the HSA-hormone binding and to confirm the Mg(2+) role on the testosterone displacement equilibrium from its HSA binding site by DHEA. Thus, both the HSA-hormone binding and the displacement equilibrium processes were reanalysed. The results obtained confirmed that:

6.
Eur J Med Chem ; 39(11): 931-7, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15501542

ABSTRACT

We report here the synthesis of aromatic coumarins and aromatic alpha-quinolones which were evaluated in vitro for their protective potentialities against tert-butyl hydroperoxide (t-BHP)-induced oxidative damage on human liver cell death, i.e., human hepatoma HepG2 cell line and human hepatocytes in primary culture. We found that the presence of a benzylidene at the 3-position or a heterocycle with N and S heteroatoms on the benzopyrone or quinolone system was essential for the protective effect of these compounds against t-BHP-induced decrease in viability of cells. We found also that a methoxy group on the aromatic ring systems decreased this potential. t-BHP-induced cytotoxicity in primary cultures of human hepatocytes could be therefore prevented by these compounds suggesting that they could display hepatoprotective effects in humans.


Subject(s)
4-Hydroxycoumarins/chemical synthesis , Carcinoma, Hepatocellular/drug therapy , Cell Survival/drug effects , Hepatocytes/drug effects , Liver Neoplasms/drug therapy , Oxidative Stress/drug effects , Quinolines/chemical synthesis , 4-Hydroxycoumarins/pharmacology , Cells, Cultured , Humans , Protective Agents/chemical synthesis , Protective Agents/pharmacology , Quinolines/pharmacology , tert-Butylhydroperoxide/adverse effects
7.
J AOAC Int ; 86(2): 222-8, 2003.
Article in English | MEDLINE | ID: mdl-12723909

ABSTRACT

The mechanism of the binding of D,L dansyl amino acids to teicoplanin was investigated. Na+ was used as an indicator of the interactions between the solutes and teicoplanin. The number (n) of sodium ions, Na+, excluded from the solute-teicoplanin interface when analyte transfer occurred was determined. A thermodynamic study and enthalpy-entropy compensation were performed to further explore the interaction mechanism. From these results, it was shown that teicoplanin was balanced between 2 conformational states characterized by distinct enantioselective properties. This approach indicates that liquid chromatography (LC) is a useful tool to extract physicochemical and molecular information from retention data. Thus, LC can be used as a complementary technique with the conventional techniques of molecular interaction analysis.


Subject(s)
Amino Acids/chemistry , Anti-Bacterial Agents/chemistry , Dansyl Compounds/chemistry , Sodium/chemistry , Teicoplanin/chemistry , Algorithms , Chromatography, Liquid , Indicators and Reagents , Stereoisomerism , Thermodynamics
8.
Article in English | MEDLINE | ID: mdl-12401375

ABSTRACT

Human serum albumin (HSA) serves as a carrier protein to transport triazine herbicides to molecular targets. In this paper, a theoretical treatment was developed to describe the HSA-triazine herbicides association. A determination of the association constant, K, as well as the degree of complexation n(c) (the percent of complex guest) was carried out. Enthalpy-entropy compensation was also analyzed in relation to this mathematical model to confirm the herbicide complexation behavior with HSA. The role of the sodium cation (Na(+)) on this association was investigated. It was expected that the sodium ion would act on the herbicide-HSA association process by modifying the surface tension of the bulk solvent and increase the K and n(c) values. The results showed that for patients who suffer from Na(+) desequilibrium, the triazine-HSA binding would change and as well the toxicological effect of these herbicides.


Subject(s)
Herbicides/metabolism , Serum Albumin/metabolism , Triazines , Humans , Sodium/metabolism , Thermodynamics
9.
Anal Chem ; 74(6): 1217-22, 2002 Mar 15.
Article in English | MEDLINE | ID: mdl-11922287

ABSTRACT

Slalom chromatography (SC) is used for the separation of large double-stranded DNA molecules. In this technique, the progression of the DNA fragments through the closed column packing follows the flow direction and is like a snake edging is way into long grass. A novel mathematical model is developed in this paper to describe this hydrodynamic phenomenon. The results obtained provided a model for the resolution between two adjacent peaks on a chromatogram. As well, a chromatographic response function was used to obtain the most efficient separation conditions for a mixture of DNA fragments with sizes higher than 15 kbp in a minimum analysis time.

10.
Biol Pharm Bull ; 25(3): 335-41, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11913529

ABSTRACT

Pharmacological studies were carried out to characterize further the endocrinological profile and the binding mode to the estrogen receptor (ER) of 6,12-dihydro-3-methoxy-1-benzopyrano[3,4-b][1,4]benzothiazin-6-one (1). Binding experiments were conducted with highly purified recombinant human estrogen receptors hERa and beta. Potent estrogenic activity of compound 1 was assessed by testing its ability to down-regulate ERs and to enhance estrogen receptor element (ERE)-dependent transcription. The latest step of our work dealt with the synthesis of the 9-fluorinated derivative 15 for ionic microscopy experiments to determine the intracellular localization of compound 1. Although 1 failed to compete with [3H]E2 for binding to both ER isoforms, evidence was reported that it interacted with hERalpha in MCF-7 cells (ER down-regulation/ERE-dependent luciferase induction). Hence, an appropriate conformation of the hormone binding domain, most probably conferred by co-regulators of ER, is required for the onset of an activity of the compound 1. Estrogenic activity was weak but on the order of magnitude of that of coumestrol (slightly weaker). The synthesis of the 9-methoxylated derivative 16 and its pharmacological evaluation led us to propose a binding mode of 1 on hERalpha. Compound 1 appears to interact with ERa mainly through interactions of its 3-methoxy substituent with the residue His-524 of the hormone binding domain.


Subject(s)
Receptors, Estrogen/agonists , Thiazines/pharmacology , Cell Line , Humans , Magnetic Resonance Spectroscopy , Radioligand Assay , Receptors, Estrogen/metabolism , Recombinant Proteins/agonists , Spectrometry, Mass, Electrospray Ionization , Thiazines/chemistry
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