RESUMEN
Theophylline still occupies a dominant place in asthma therapy. Unfortunately its adverse central nervous system (CNS) stimulant effects can dramatically limit its use, and adjustments in the dosage are often needed. We have synthesized a new series of imidazo[1,2-alpha]pyrazine derivatives which are much more potent bronchodilators than theophylline in vivo and do not exhibit the CNS stimulatory profile. In vitro studies on isolated rat uterus and guinea pig trachea confirm the high potentialities of these derivatives. 6-Bromo-8-(methylamino)imidazo[1,2-alpha]-pyrazine-3-carbonitrile (23) is identified as the most potent compound of the series. As in the case of theophylline, phosphodiesterase inhibition appears unlikely to be the unique mechanism of action of this series of heterocycles.
Asunto(s)
Broncodilatadores/síntesis química , Imidazoles/síntesis química , Pirazinas/síntesis química , Animales , Broncodilatadores/farmacología , Imidazoles/farmacología , Técnicas In Vitro , Masculino , Ratones , Actividad Motora/efectos de los fármacos , Inhibidores de Fosfodiesterasa/farmacología , Pirazinas/farmacología , Relación Estructura-Actividad , Teofilina/farmacologíaRESUMEN
Molecular biotransformation of 2-phenylthiazolidine (1) and its m-bromo derivative (2) in the mouse is followed by autoradiographic studies and assessed by analysis of urinary metabolites. Cysteamine (4) is one of the metabolites of compounds 1 and 2. Radioprotective activity and efficacy over a period of time of 1, 2, and 4 correlate closely with distribution and metabolism.
Asunto(s)
Protectores contra Radiación/metabolismo , Tiazoles/metabolismo , Animales , Benzaldehídos/metabolismo , Biotransformación , Cromatografía en Capa Delgada , Cisteamina/metabolismo , Ratones , TiazolidinasRESUMEN
A series of imidazo[1,2-alpha]pyrazine derivatives was synthesized by condensation of alpha-halogenocarbonyl compounds and aminopyrazines. Various compounds resulted from competitive reactions or reagent isomerization and demonstrated in vitro uterine-relaxing and in vivo antibronchospastic activities. On isolated atria, 5-bromoimidazo-[1,2-alpha]pyrazine showed positive chronotropic and inotropic properties; the latter was associated with an increase in the cyclic AMP tissue concentration. Potentiation of the isoproterenol positive inotropic effect of 5-bromoimidazo[1,2-alpha]pyrazine and the lack of blockade of the 5-bromoimidazo[1,2-alpha]pyrazine positive inotropic effect by propranolol suggested phosphodiesterase-inhibiting properties.
Asunto(s)
Espasmo Bronquial/tratamiento farmacológico , Corazón/efectos de los fármacos , Imidazoles/farmacología , Pirazinas/farmacología , Contracción Uterina/efectos de los fármacos , Animales , Función Atrial , Fenómenos Químicos , Química , AMP Cíclico/metabolismo , Relación Dosis-Respuesta a Droga , Interacciones Farmacológicas , Femenino , Cobayas , Frecuencia Cardíaca/efectos de los fármacos , Imidazoles/síntesis química , Isoproterenol/farmacología , Masculino , Contracción Miocárdica/efectos de los fármacos , Propranolol/farmacología , Ratas , Estimulación Química , Relación Estructura-ActividadRESUMEN
The synthesis of original imidazo[1,2-a]pyridines bearing a thioether side chain at the 3 position and their antiviral activity are reported. From the synthesized compounds, 4, 15, and 21 were highly active against human cytomegalovirus with a therapeutic index superior to 150. These compounds also showed pronounced activity against varicella-zoster virus. Their structure-activity relationship is discussed.
Asunto(s)
Antivirales/síntesis química , Imidazoles/síntesis química , Piridinas/síntesis química , Animales , Antivirales/química , Antivirales/farmacología , Línea Celular , Chlorocebus aethiops , Citomegalovirus/efectos de los fármacos , Evaluación Preclínica de Medicamentos , Células HeLa , Herpesvirus Humano 3/efectos de los fármacos , Humanos , Imidazoles/química , Imidazoles/farmacología , Concentración 50 Inhibidora , Piridinas/química , Piridinas/farmacología , Relación Estructura-Actividad , Células VeroRESUMEN
The synthesis and the antiviral activities of C-3 acyclic nucleoside analogues of imidazo[1,2-a]pyridine and pyrimidine are reported. From these compounds, 20, 21, 22, 23, 28, and 34 showed a specific activity against cytomegalovirus and/or varicella-zoster virus.
Asunto(s)
Antivirales/síntesis química , Nucleósidos/síntesis química , Piridinas/química , Piridinas/síntesis química , Pirimidinas/síntesis química , Animales , Antivirales/farmacología , Chlorocebus aethiops , Células HeLa , Humanos , Nucleósidos/farmacología , Piridinas/farmacología , Pirimidinas/farmacología , Relación Estructura-Actividad , Células Tumorales Cultivadas , Células VeroRESUMEN
1. Experiments have been performed in order to analyse the mechanism whereby SCA40, a new imidazo[1,2-a]pyrazine derivative relaxes airway smooth muscle. 2. SCA40 (0.01-10 microM) caused a complete and concentration-dependent relaxation of guinea-pig isolated trachea contracted with 20 mM KCl but failed to inhibit completely the spasmogenic effects of 80 mM KCl. 3. Quinine (30 microM) antagonized the relaxant activity of SCA40 in 20 mM KCl-contracted guinea-pig isolated trachea. The ATP-sensitive K(+)-channel blocker, glibenclamide (3 microM), did not antagonize the relaxant activity of SCA40 in either 20 mM KCl or 1 microM carbachol-contracted isolated trachea. 4. SCA40 (0.01-10 microM) and isoprenaline (0.1 nM-10 microM) caused a complete and concentration-dependent relaxation of guinea-pig isolated trachea contracted with carbachol 1 microM. 5. The large-conductance Ca(2+)-activated K(+)-channel blocker, charybdotoxin (60-180 nM), non-competitively antagonized the relaxant activity of isoprenaline on 1 microM carbachol-contracted trachea. The inhibition was characterized by rightward shifts of the isoprenaline concentration-relaxation curves with depression of their maxima. 6. The relaxant activity of SCA40 in 1 microM carbachol-contracted trachea was antagonized by charybdotoxin (60-600 nM) in an apparently competitive manner. The concentration-relaxation curves to SCA40 were shifted to the right with no significant alteration in the maximum response. 7. It is concluded that SCA40 is a novel potassium channel opener which is a potent relaxant of guinea-pig airway smooth muscle in vitro. The relaxant activity of SCA40 does not involve ATP-sensitive K+-channels but rather large-conductance Ca2'-activated K+-channels or other charybdotoxin sensitive K+-channels.
Asunto(s)
Imidazoles/farmacología , Canales de Potasio/efectos de los fármacos , Pirazinas/farmacología , Venenos de Escorpión/farmacología , Tráquea/metabolismo , Animales , Carbacol/farmacología , Caribdotoxina , Gliburida/farmacología , Cobayas , Técnicas In Vitro , Isoproterenol/farmacología , Masculino , Contracción Muscular/efectos de los fármacos , Relajación Muscular/efectos de los fármacos , Tono Muscular/efectos de los fármacos , Cloruro de Potasio/farmacología , Tráquea/efectos de los fármacosRESUMEN
1. Experiments have been performed to investigate the cardiovascular actions in the rat of SCA40, a novel potassium channel opener which is a potent relaxant of guinea-pig airway smooth muscle in vivo and in vitro. 2. SCA40 (0.01-30 microM) caused a complete and concentration-dependent relaxation of rat isolated thoracic aorta contracted with 20 mM KCl but failed to inhibit completely the spasmogenic effects of 80 mM KCl. 3. The ATP-sensitive K(+)-channel blocker, glibenclamide (3 microM), failed to antagonize the relaxant action of SCA40 on 20 mM KCl-contracted rat isolated thoracic aorta. 4. SCA40 (0.001-100 microM) had dual effects on rat isolated atria. At low concentrations, SCA40 produced a concentration-dependent decrease in the rate and force of contractions. At higher concentrations (greater than 1 microM) SCA40 induced concentration-dependent increases of atrial rate and force. 5. In vivo, in normotensive Wistar rats, SCA40 elicited a dose-dependent (1-100 micrograms kg-1) decrease in mean arterial pressure which was accompanied by a moderate dose-dependent increase in heart rate. SCA40 (100 micrograms kg-1) had a slightly greater hypotensive effect than cromakalim (100 micrograms kg-1) but the duration of the hypotension was longer with cromakalim than with SCA40. 6. The hypotensive effect of SCA40 was not reduced by propranolol, atropine, NG-nitro-L-arginine methyl ester (L-NAME) or glibenclamide. 7. It is concluded that the mechanism by with SCA40 relaxes vascular smooth muscle in vitro and in vivo involves activation of K(+)-channels distinct from glibenclamide-sensitive ATP-sensitive K(+)-channels.
Asunto(s)
Sistema Cardiovascular/efectos de los fármacos , Imidazoles/farmacología , Parasimpatolíticos/farmacología , Canales de Potasio/efectos de los fármacos , Pirazinas/farmacología , Animales , Aorta Torácica/efectos de los fármacos , Presión Sanguínea/efectos de los fármacos , Cardiotónicos/farmacología , Relación Dosis-Respuesta a Droga , Interacciones Farmacológicas , Atrios Cardíacos/efectos de los fármacos , Frecuencia Cardíaca/efectos de los fármacos , Isoproterenol/farmacología , Masculino , Relajación Muscular/efectos de los fármacos , Músculo Liso Vascular/efectos de los fármacos , Contracción Miocárdica/efectos de los fármacos , Propranolol/farmacología , Ratas , Ratas WistarRESUMEN
Theophylline and other methylxanthines display a large number of biological effects, some of which are clinically important. The effects of these compounds are commonly ascribed to an inhibition of cyclic AMP breakdown. However, it becomes actually evident that another mechanism, namely adenosine receptor antagonism, could be responsible for certain methylxanthine effects. It could be of interest to find new compounds displaying only one of these mechanisms, either phosphodiesterase inhibition or adenosine receptor antagonism. We have studied several synthetic imidazol[1,2a]pyrazines, some of which display theophylline-like pharmacological properties at lower doses than theophylline. We showed that some of these compounds inhibited mitogen-induced [3H]-thymidine uptake by human lymphocytes, which is consistent with increases in cyclic AMP levels: the most efficient compounds were those which were better phosphodiesterase inhibitors than theophylline and poorer adenosine receptor antagonists.
Asunto(s)
Teofilina/farmacología , Xantinas/farmacología , 3',5'-AMP Cíclico Fosfodiesterasas/antagonistas & inhibidores , Adenosina/análogos & derivados , Adenosina/farmacología , Adenosina-5'-(N-etilcarboxamida) , Adenilil Ciclasas/metabolismo , Adulto , Animales , Femenino , Humanos , Técnicas In Vitro , Masculino , Ratones , Pirazinas/farmacología , Receptores de Superficie Celular/efectos de los fármacos , Receptores Purinérgicos , Timidina/metabolismoRESUMEN
Crucial conditions for the pharmacological use of active compounds are their ability to cross the biological barriers and reach their intracellular target. In the case of two antiviral pyridopurine derivatives, 1 and 2, this included essentially the membranes and the nucleic acids. Thus the interactions of 1 and 2 with model membranes and oligonucleotides were studied using NMR spectroscopy. It was found that these hydrophobic molecules can be incorporated into the model membranes at the terminal methyl group level, inducing dynamic perturbations in the bilayer. In the presence of the synthetic oligonucleotide ACATGT, both molecules can intercalate aspecifically in AT and GC systems. Inclusion complexes of 1 and 2 beta-cyclodextrins with a 1:1 stoichiometry, were also prepared. This led to to propose two galenic forms 1 and 2, i.e. included in phospholipid vesicles in the form of a beta-cyclodextrin complex
Asunto(s)
Aminas/química , Ciclodextrinas/química , Preparaciones Farmacéuticas/química , Dimiristoilfosfatidilcolina/química , Alimentos , Espectroscopía de Resonancia MagnéticaRESUMEN
Gd-DOTA contrast enhancement of MR images was evaluated on induced mammary tumors in female rats. A single intravenous injection of the carcinogenic N-nitrosourea ENU was administered to Wistar rats; this simple treatment led to a high percentage of mammary tumors without causing death. All the induced tumors were adenocarcinoma and their heterogeneousness depended on their size. The induced tumors did not have intra- or extravascular inflammatory spaces caused by heterotopic lesions, as is the case with implanted tumors. Before injection of Gd-DOTA, appearance of the patchy internal structure was clearly demonstrated on spin-echo images performed with long repetition times. Three doses of the paramagnetic contrast agent (0.1, 0.2, and 0.5 mmol/kg) were evaluated on two different T1-weighted MR sequences. Images were recorded before and repeatedly after intravenous injection of Gd-DOTA, and signal intensities and relaxation times were measured. On images acquired with the spin-echo 500/28 as well as the inversion-recovery 928/26/300 sequences, the results showed that 0.2 mmol/kg Gd-DOTA was the optimal dose for contrast enhancement and for clear visualization of the heterogeneousness of the mammary tumor.
Asunto(s)
Adenocarcinoma/diagnóstico , Gadolinio , Compuestos Heterocíclicos , Imagen por Resonancia Magnética/métodos , Neoplasias Mamarias Experimentales/diagnóstico , Compuestos Organometálicos , Animales , Medios de Contraste/administración & dosificación , Femenino , Ratas , Ratas Endogámicas , Factores de TiempoRESUMEN
Changing different parameters involved in imaging procedures, paramagnetic substances provide contrast enhancement in MRI. Contrast agents presently studied in animals and clinical trials, are either salts or complexes of mineral ions either nitroxide stable free radicals. Their development should extend the possibilities of tissular characterization and functional or metabolic evaluation of the MRI.
Asunto(s)
Medios de Contraste , Espectroscopía de Resonancia Magnética , Animales , Medios de Contraste/efectos adversos , Radicales Libres , Gases , Humanos , MineralesRESUMEN
Asthma is a complex disease characterised by bronchoconstriction and airways inflammation. Recent advances in medicinal chemistry will surely lead to a better reappraisal of therapeutic strategies. 8-(Methylamino)imidazo(1,2-a)pyrazines with substitution either on position 2 or 3 powerful relaxing agents in vitro as well as in vivo in animals. 6-Bromo-8-(methylamino)imidazo[1,2-a]pyrazine- 2-carbonitrile, SCA40, is a new and potent bronchodilator. Chemical synthesis of such a series of derivatives involves a condensation reaction with formation of the imidazole ring and/or diverse electrophilic substitutions. Chemical reactivity of the heterocycle can be modulated by introduction on position 8 of electrodonating groups that highly favor electrophilic substitution on position 3. Interestingly, lithiation studies on the heterocycle exhibit regioselectivity, leading either to an halogen exchange when position 3 is occupied by a bromine atom or an ortho-directed metalation in accord with the presence of an halogen on position 6.
Asunto(s)
Broncodilatadores/síntesis química , Imidazoles/síntesis química , Pirazinas/síntesis química , Broncodilatadores/química , Broncodilatadores/farmacología , Imidazoles/química , Imidazoles/farmacología , Pirazinas/química , Pirazinas/farmacología , Relación Estructura-ActividadRESUMEN
Three potentially antiviral imidazo[1,2-a]pyridine derivatives of increasing hydrophilicity were tested in their interactions with model membranes and synthetic oligonucleotides. It was shown that the most hydrophobic derivative [1], located in the depth of the bilayer only induces minor membrane damages. The molecule [2], only poorly hydrophobic, integrates also the bilayer in the medium part of the chains while the most hydrophilic [3] exhibits fluidizing and slightly detergent properties. In the presence of synthetic oligonucleotide ACATGT no intercallation of the three derivatives was evidenced. By considering their antiviral activity in the absence of evident mitogenic properties, another mechanism of action was proposed.
Asunto(s)
Antivirales/química , Imidazoles/química , Piridinas/química , Membrana Dobles de Lípidos/química , Espectroscopía de Resonancia Magnética , Membranas Artificiales , Oligonucleótidos/químicaRESUMEN
Experiments have been performed in order to analyse the mechanism whereby SCA40, a new imidazo[1,2-a]pyrazine derivative relaxes airway smooth muscle. We investigated the effect of different toxins, known to be K(+)-channel blockers on guinea-pig smooth muscle relaxant activity of SCA40. The small conductance Ca(2+)-activated K(+)-channel blocker apamin (100 nM) did not antagonize the relaxant activity of SCA40 in 1 microM carbachol-contracted isolated guinea pig trachea. The large conductance Ca(2+)-activated K(+)-channel blocker, iberiotoxin (30, 60 and 180 nM) antagonized the relaxant activity of SCA40 in an apparently competitive manner. The concentration-relaxation curves to SCA40 were shifted to the right with no significant alteration in the maximum response. The relaxant activity of SCA40 in 1 microM carbachol-contracted isolated trachea was antagonized by both charybdotoxin (60 nM) and iberiotoxin (60 nM), but the antagonism induced by iberiotoxin appears to be more potent than that induced by charybdotoxin. It is concluded that the potent relaxant activity of SCA40 on guinea-pig airway smooth muscle in vitro involves a charybdotoxin and iberiotoxin sensitive K(+)-channel.
Asunto(s)
Apamina/farmacología , Imidazoles/farmacología , Relajación Muscular/efectos de los fármacos , Músculo Liso/fisiología , Parasimpatolíticos/farmacología , Péptidos/farmacología , Pirazinas/farmacología , Venenos de Escorpión/farmacología , Animales , Caribdotoxina , Cobayas , Técnicas In Vitro , Masculino , Canales de Potasio/metabolismo , TráqueaRESUMEN
The smooth muscle relaxant activity and other pharmacological properties of imidazo[1,2-alpha]pyrazine derivatives were compared with those of theophylline. Imidazo[1,2-alpha]pyrazine derivatives exhibited a potent smooth muscle relaxant activity regardless of the agent which had elicited the contraction and thus showed a broad spectrum of non specific smooth muscle relaxant activity. In the isolated guinea-pig atria, imidazo[1,2-alpha]pyrazine derivatives exhibited potent inotropic and chronotropic activities. As opposed to theophylline, the imidazo[1,2-alpha]pyrazine derivatives tested were unable to antagonize the adenosine-induced inhibition of spontaneous contractile activity of rabbit ileum. Furthermore, as opposed to theophylline, these derivatives did not exhibit a marked diuretic activity. Thus it appears that they do not act as adenosine receptor antagonists. Imidazo[1,2-alpha]pyrazine derivatives inhibited the total cAMP-phosphodiesterase (cAMP-PDE) and the total cGMP-phosphodiesterase (cGMP-PDE) activities of bovine trachea but with relatively low potencies, sharing a discrepancy between their activity on isolated tissues and their ability to inhibit PDE. It is suggested that imidazo[1,2-alpha]pyrazine derivatives may selectively inhibit type III and/or type IV phosphodiesterase isoenzymes involved in the regulation of the mechanical activity of cardiac and smooth muscle tissues.
Asunto(s)
Imidazoles/farmacología , Parasimpatolíticos/farmacología , Inhibidores de Fosfodiesterasa/farmacología , Pirazinas/farmacología , Adenosina/antagonistas & inhibidores , Adenosina/farmacología , Animales , Calcio/farmacología , Fármacos Cardiovasculares/farmacología , Bovinos , Diuresis/efectos de los fármacos , Cobayas , Atrios Cardíacos/efectos de los fármacos , Frecuencia Cardíaca/efectos de los fármacos , Íleon/efectos de los fármacos , Técnicas In Vitro , Masculino , Contracción Muscular/efectos de los fármacos , Relajación Muscular/efectos de los fármacos , Músculo Liso/efectos de los fármacos , Contracción Miocárdica/efectos de los fármacos , Conejos , Ratas , Ratas Wistar , Teofilina/farmacología , Tráquea/efectos de los fármacosRESUMEN
N-1 and N-2 substituted pyrazolo[4,5-g]pyrido[1,2-a]benzimidazoles were prepared regioselectively, and cytotoxicities evaluated in vitro against K562 and HL60 cells. All compounds displayed weaker activity than doxorubicin against sensitive lines, but showed the same activity against resistant cell lines (multidrug resistance+, (MDR+); K562R and HL60R) indicating no resistance phenomena.
Asunto(s)
Antineoplásicos/síntesis química , Bencimidazoles/síntesis química , Antibióticos Antineoplásicos/farmacología , Antineoplásicos/farmacología , Bencimidazoles/farmacología , Doxorrubicina/farmacología , Células HL-60 , Humanos , Células K562 , Espectroscopía de Resonancia Magnética , Células Tumorales CultivadasRESUMEN
The longitudinal relaxivities of seven water-soluble nitroxide derivatives of low-molecular weight have been measured at 5 degrees C and 37 degrees C in water and in serum between 0.01 and 200 MHz. The nuclear magnetic relaxation dispersion (NMRD) profiles show a clear relationship between the relaxivity observed in serum and the relative balance of the hydrophobic/hydrophilic character of the paramagnetic molecules. From the data analysis, contributions arising from a population of nitroxides characterized by reduced mobility can be extracted. The values of the correlation times are consistent with a system involving nitroxides adsorbed at the surface of albumin and magnetically interacting with the protons of hydrogen bonded water molecules.
Asunto(s)
Óxidos de Nitrógeno/química , Óxidos N-Cíclicos , Radicales Libres , Humanos , Espectroscopía de Resonancia Magnética , Peso Molecular , Óxidos de Nitrógeno/sangre , Marcadores de Spin , Relación Estructura-Actividad , AguaRESUMEN
Benzonitriles have been evaluated as potential antiradiation agents in mice. They have an interesting radioprotective activity, in particular 3,5-dinitrobenzonitrile, one of the non-sulfur-containing radioprotective compounds which presents a consistent DRF (DRF = 1.35).
Asunto(s)
Nitrilos/síntesis química , Protectores contra Radiación/síntesis química , Animales , Relación Dosis-Respuesta en la Radiación , Ratones , Nitrilos/farmacología , Factores de TiempoRESUMEN
Access to the original series of pyrido[1',2':1,2]imidazo[4,5-h]quinazoline was developed from a 1,3-dicarbonyl unit with some "N-C-N" bisnucleophilic reagents and the derivatives obtained were evaluated for in vitro cytotoxic activities against HL60 and A2780 cells. All compounds exhibited cytotoxic activities on resistant cell lines (MDR+; HL60R and A2780R) with no resistance phenomena.
Asunto(s)
Antineoplásicos/síntesis química , Antineoplásicos/farmacología , Bencimidazoles/síntesis química , Bencimidazoles/farmacología , Quinazolinas/síntesis química , Quinazolinas/farmacología , Animales , Supervivencia Celular/efectos de los fármacos , Resistencia a Antineoplásicos , Genes MDR/genética , Células HL-60 , Humanos , Inmunohistoquímica , Indicadores y Reactivos , Ratones , Células Tumorales CultivadasRESUMEN
Several diaza-analogs of phenanthrene derived from 3-amino, 5-amino, 6-amino, 8-aminoquinolines, and 5-aminoisoquinoline were prepared to evaluate their antiplasmodial activities. All compounds showed mild to good activitiy in vitro, both on a Nigerian chloroquino-sensitive strain and on the chloroquino-resistant FcB1-Columbia and FcM29 strains. The position of the intracyclic nitrogen atom is shown to be crucial for the activities (best results are obtained with a 1,10-phenanthroline skeleton). In regard to the particular properties of this structure (metalloprotease inhibition activitiy by chelating divalent metal ions), the potential chelating site of the molecule was blocked. In this case, the biological activity of the compound was greatly enhanced, showing that the mechanism of action of such a compound is probably not correlated to metalloprotease inhibition activity.