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1.
Sci Justice ; 57(5): 349-360, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28889864

RESUMEN

In recent years there has been growing interest in environmental forms of trace evidence, and ecological trace evidence collected from footwear has proved valuable within casework. Simultaneously, there has been growing awareness of the need for empirical experimentation to underpin forensic inferences. Diatoms are unicellular algae, and each cell (or 'frustule') consists of two valves which are made of silica, a robust material that favours their preservation both in sediments and within forensic scenarios. A series of experiments were carried out to investigate the transfer and persistence of diatoms upon common footwear materials, a recipient surface that has historically been overlooked by studies of persistence. The effectiveness of two novel extraction techniques (jet rinsing, and heating and agitation with distilled water) was compared to the established extraction technique of hydrogen peroxide digestion, for a suite of five common footwear materials: canvas, leather, and 'suede' (representing upper materials), and rubber and polyurethane (representing sole materials). It was observed that the novel extraction technique of heating and agitation with distilled water did not extract fewer diatom valves, or cause increased fragmentation of valves, when compared to peroxide digestion, suggesting that the method may be viable where potentially hazardous chemical reactions may be encountered with the peroxide digestion method. Valves could be extracted from all five footwear materials after 3min of immersion, and more valves were extracted from the rougher, woven upper materials than the smoother sole materials. Canvas yielded the most valves (a mean of 2511/cm2) and polyurethane the fewest (a mean of 15/cm2). The persistence of diatoms on the three upper materials was addressed with a preliminary pilot investigation, with ten intervals sampled between 0 and 168h. Valves were seen to persist in detectable quantities after 168h on all three upper materials. However, some samples produced slides with no valves, and the earliest time after which no diatom valves were found was 4h after the transfer. Analysis of the particle size distributions over time, by image analysis, suggests that the retention of diatoms may be size-selective; after 168h, no particles larger than 200µm2 could be found on the samples of canvas, and >95% of the particles on the samples of suede were less than or equal to 200µm2. A pilot investigation into the effects of immersion interval was carried out upon samples of canvas. Greater numbers of valves were extracted from the samples with longer immersion intervals, but even after 30s, >500 valves could be recovered per cm2, suggesting that footwear may be sampled for diatoms even if the contact with a water body may have been brief. These findings indicate that, if the variability within and between experimental runs can be addressed, there is significant potential for diatoms to be incorporated into the trace analysis of footwear and assist forensic reconstructions.


Asunto(s)
Diatomeas , Agua Dulce , Zapatos , Manejo de Especímenes/métodos , Diatomeas/aislamiento & purificación , Ciencias Forenses , Humanos , Inmersión
2.
Diabetes Obes Metab ; 15(10): 954-7, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23551951

RESUMEN

Antihyperglycaemic therapy on bone was evaluated in the ovariectomized (OVX), non-diabetic adult rat. Animals were treated daily for 12 weeks with various doses of sitagliptin, pioglitazone, rosiglitazone, combinations of sitagliptin with pioglitazone or vehicle alone. Sitagliptin target engagement was confirmed by assessing inhibition of plasma dipeptidyl peptidase-4 (DPP-4) and oral glucose tolerance. Parameters related to bone health were evaluated in femur and vertebrae by dual-energy X-ray absorptiometry and histomorphometry. Bone mineral density (BMD) generally did not differ significantly between OVX-sitagliptin-treated animals and OVX-vehicle controls. In lumbar vertebrae, however, there was significantly less BMD loss with increasing sitagliptin dose. Thiazolidinedione (TZD) treatment generally resulted in lower BMD; OVX-TZD-treated (but not OVX-sitagliptin-treated) animals also had lessened cortical thickness in central femur and profoundly greater bone marrow adiposity in lumbar vertebrae. These findings support prior findings with TZDs and suggest a neutral or beneficial impact of DPP-4 inhibition on bone health.


Asunto(s)
Densidad Ósea/efectos de los fármacos , Hipoglucemiantes/farmacología , Pirazinas/farmacología , Tiazolidinedionas/farmacología , Triazoles/farmacología , Absorciometría de Fotón , Animales , Progresión de la Enfermedad , Estrógenos/deficiencia , Femenino , Fémur/efectos de los fármacos , Fémur/patología , Humanos , Vértebras Lumbares/efectos de los fármacos , Vértebras Lumbares/patología , Ovariectomía , Ratas , Fosfato de Sitagliptina
3.
Bioorg Med Chem ; 21(11): 3272-9, 2013 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-23602623

RESUMEN

In this paper, we investigated the previously synthesized anticonvulsant enaminone ethyl ester analogs using the computational gaussian 03 programs. The significant chemical features of the enaminone compounds that lead to positive anticonvulsant activity were identified. From our analyses, we believe that the neutrality of the phenyl ring may be important for binding in the hydrophobic pocket of the active site and that the binding of the phenyl substituent is the main reason why some analogs are active and others are inactive.


Asunto(s)
Compuestos de Anilina/química , Anticonvulsivantes/química , Etanol/análogos & derivados , Etanol/química , Modelos Moleculares , Sitios de Unión , Diseño de Fármacos , Ésteres , Humanos , Interacciones Hidrofóbicas e Hidrofílicas , Electricidad Estática , Relación Estructura-Actividad , Termodinámica
4.
Sci Justice ; 63(3): 376-386, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-37169463

RESUMEN

Environmental trace evidence offers useful circumstantial intelligence to link persons and scenes of forensic interest. An increasing empirical research base is dedicated towards understanding the transfer and persistence dynamics of environmental indicators including pollen, soils, and diatoms, within a diverse range of experimental frameworks. This paper presents two discrete studies exploring transfer and persistence of soils and sediments on footwear and diatomaceous earth adhered to clothing in forensically pertinent scenarios. Variables including sediment type, foot position, clothing type, and body positioning were also explored throughout. Both experiments incorporated a field-based methodology during the sampling effort. Photographs were collected of an initial transfer sample and of a retained assemblage following hours, days, and up to one-week of wear, facilitating macroscopic assessment of trace evidence dynamics. All images were processed using accessible, open-source software before spatial analysis of evidence distribution within and temporal assessment (% retention) upon each evidential surface. The results highlighted consistent loss of transferred sediment from footwear with significantly greater retention of loamy clay soil than dune sand which was absent beyond 24 h of wear. Loss was not influenced by wearer gait but was more rapid from those areas of the shoe sole in direct contact with the ground. Diatomaceous earth was retrieved from all three clothing types tested after one week - significant losses of material occurred before 48 h with a consistent assemblage identified beyond this. Denim was significantly more effective than acrylic and fleece for diatomaceous earth retention and significantly more material was lost from clothing worn on the lower body. These findings highlight the value of using visual environmental markers and a macroscopic analytical approach during the investigation of environmental trace dynamics. The methodology offers a novel, non-destructive assessment of soil and diatom transfer and persistence, complementing more extensive laboratory-based examinations to ensure the development of a well-rounded research base within the forensic sciences.


Asunto(s)
Vestuario , Tierra de Diatomeas , Humanos , Medicina Legal , Zapatos , Ciencias Forenses/métodos , Suelo
5.
Forensic Sci Int ; 325: 110898, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-34247142

RESUMEN

Freshwater diatoms offer valuable circumstantial forensic indicators, with a growing empirical research base aiming to identify and understand some of the spatial and temporal factors affecting their validity as trace evidence. Previous studies demonstrated that recipient surface characteristics, environmental variability, and individual species traits influence the initial transfer of freshwater diatoms to clothing. However, no previous research has sought to consider the impact of these and other variables on the persistence of transferred diatoms over investigative timescales. Therefore, this study aimed to identify and explore diatom retention dynamics on clothing following wear over time (hours to weeks). A series of experiments were designed to examine the impact of clothing material, seasonality, and time since wear (persistence interval) on the total number and species-richness of diatoms recovered and their relative retention (%) over time. Nine clothing swatches were immersed in a freshwater environment and then worn for one month in the spring. Subsamples were retrieved at regular intervals (e.g. 30 mins, 1 h, 8 h, 24 h) up to one month, diatoms were extracted using a H2O2 method, and examined microscopically. Three clothing materials were subject to the same experiment in the winter to generate a seasonal comparison. The results broadly identified three stages of diatom persistence on clothing - rapid initial loss, variable intermediate decay, and sustained long-term presence. Clothing material significantly impacted the number of diatoms recovered and retention dynamics over time, with complex interactions identified with seasonality. Although fewer diatoms were recovered in the winter, overall retention trends were consistent at the different times of year. The findings demonstrate that diatoms can be recovered from clothing, even weeks or months after an initial transfer, yielding a useful environmental trace indicator for forensic reconstructions over investigative timescales. The impact of clothing material and seasonality on persistence identified cotton, acrylic, and viscose clothing as the most reliable temporal repository of diatom trace evidence, with a more abundant forensic assemblage available for forensic comparisons in the spring.


Asunto(s)
Vestuario , Diatomeas , Agua Dulce , Ciencias Forenses , Humanos , Estaciones del Año , Manejo de Especímenes
6.
Forensic Sci Int ; 326: 110897, 2021 Jul 04.
Artículo en Inglés | MEDLINE | ID: mdl-34411937

RESUMEN

Diatoms are a useful form of environmental trace evidence, yielding a circumstantial link between persons and scenes of forensic interest. A developing empirical research base has sought to understand those factors affecting the transfer and persistence of freshwater diatoms on clothing and footwear surfaces. Although an initial study has demonstrated that diatoms can persist on clothing following weeks of wear, no previous research has explored the temporal dynamics of a persistent species assemblage over timescales pertinent to forensic investigations. This study therefore aimed to determine if: (1) valve morphology (size and shape) influences diatom persistence, (2) the relative abundance of taxa within an assemblage affects retention, and (3) a persistent diatom assemblage retrieved from clothing after one month can reliably be compared to the site of initial transfer. To build on previous research findings which highlighted the impact of substrate and environmental seasonality on diatom transfer and persistence, here, nine clothing materials were tested in spring before a seasonal comparison in the winter. Fabric swatches were immersed in a freshwater river, worn attached to clothing, and subsamples retrieved at regular intervals (hours, days, weeks) up to one month post-immersion. Diatoms were extracted using a H2O2 technique and analysed via microscopy. The results indicated that smaller diatoms (< 10 µm) are retained in significantly greater abundance, with no statistically significant difference between centric and pennate diatom loss over time. Although a persistent species assemblage was relatively stable over the one month of wear, significant differences were identified between clothing substrate in the spring and between the seasonal samples. The most abundant environmental taxa were consistently identified in the forensic samples, with greater variability attributed to the retention of relatively less common species. The findings suggest that, despite a loss in the abundance and species-richness of diatoms retrieved from clothing over time, a persistent assemblage may provide a useful circumstantial link to the site of initial transfer. The complex relationships between clothing type, environmental seasonality, and time since wear on retention, emphasise the need for diatom trace evidence to be carefully interpreted within an exclusionary framework, and the significance of any casework findings to be determined with reference to empirical evidence bases.

7.
Bioorg Med Chem ; 17(14): 5342-6, 2009 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-19559624

RESUMEN

This article expands upon our original submission to the Eddington, N. D.; Cox, D. S.; Khurana, M.; Salama, N. N.; Stables, J. P.; Harrison, S. J.; Negussie, A.; Taylor, R. S.; Tran, U. Q.; Moore, J. A.; Barrow, J. C.; Scott, K. R. Eur. J. Med. Chem.2003, 38, 49 on a series of twenty (20) compounds, all 5-methyl-3-[(substituted)-phenylamino]-cyclohex-2-enone derivatives. This article provides the reasons why the compounds are active/inactive. By use of computational methods, the reasons for activity/inactivity are explained.


Asunto(s)
Anticonvulsivantes/química , Anticonvulsivantes/farmacología , Ciclohexanonas/química , Ciclohexanonas/farmacología , Simulación por Computador , Modelos Químicos , Modelos Moleculares , Estructura Molecular , Relación Estructura-Actividad
8.
Bioorg Med Chem ; 17(1): 133-40, 2009 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-19059784

RESUMEN

3D-QSAR studies comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) were carried out on 26 structurally diverse subcutaneous pentylenetetrazol (scPTZ) active enaminone analogues, previously synthesized in our laboratory. CoMFA and CoMSIA were employed to generate models to define the specific structural and electrostatic features essential for enhanced binding to the putative GABA receptor. The 3D-QSAR models demonstrated a reliable ability to predict the CLogP of the active anticonvulsant enaminones, resulting in a q(2) of 0.558 for CoMFA, and a q(2) of 0.698 for CoMSIA. The outcomes of the contour maps for both models provide detailed insight for the structural design of novel enaminone derivatives as potential anticonvulsant agents.


Asunto(s)
Aminas/química , Anticonvulsivantes/química , Antagonistas del GABA/química , Relación Estructura-Actividad Cuantitativa , Diseño de Fármacos , Humanos , Modelos Moleculares , Pentilenotetrazol , Receptores de GABA/química , Receptores de GABA/metabolismo
9.
Sci Justice ; 59(3): 292-305, 2019 05.
Artículo en Inglés | MEDLINE | ID: mdl-31054818

RESUMEN

Environmental indicators are increasingly sought and analysed in a range of forensic reconstructions. Although the majority of casework and research studies are concerned with the criminal investigation of terrestrial habitats (soils, sediments, plants etc.), freshwater environments are also frequently encountered as crime scenes. As such, microalgae, particularly diatoms, may provide useful circumstantial trace evidence following their transfer to a victim or perpetrator. Diatom analysis is a relatively underused technique in forensic ecology, although an increased empirical research focus is beginning to recognise the evidential value of a transferred assemblage. This study aimed to examine three of the spatial and temporal variables known to influence the extent of an initial transfer of trace particulates, within the context of freshwater diatoms to clothing. A series of experiments were designed to consider the impact of recipient surface characteristics (clothing type), source environment conditions (seasonality), and morphological (type of diatom) variability, on the total number (no. per cm2) and species richness (total no. sp.) of an evidential diatom sample recovered from clothing. Nine commonly used clothing materials were immersed in a freshwater river at three times of year - the early and late spring and in the winter. Diatoms were recovered using a H2O2 extraction technique and examined microscopically. The results demonstrated that diatom transfer to clothing varies significantly, with a greater abundance and a higher species richness transferred to coarse woven surfaces including acrylic, linen, and viscose. Significantly fewer diatoms were transferred to clothing in the winter, in line with seasonal fluctuations in the source environment diatom community. Furthermore, variation in the relative abundance of particular diatom species was identified between clothing types, provisionally suggesting that morphological characteristics may also support or limit the transfer of material. These findings highlight that, although clothing may offer a valuable repository of freshwater diatom trace evidence, the interpretation of evidential material should be approached within an exclusionary framework. Thus, empirical data has been generated to develop evidence bases within forensic ecology, demonstrating some of the spatial and temporal factors which may contribute to or limit the transfer of evidence.


Asunto(s)
Vestuario , Diatomeas/clasificación , Diatomeas/aislamiento & purificación , Análisis Espacio-Temporal , Ciencias Forenses/métodos , Agua Dulce/análisis , Microscopía/métodos , Estaciones del Año
10.
J Pharm Sci ; 96(10): 2509-31, 2007 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17621683

RESUMEN

Enaminones, enamines of beta-dicarbonyl compounds, have been known for many years. Their early use has been relegated to serving as synthetic intermediates in organic synthesis and of late, in pharmaceutical development. Recently, the therapeutic potential of these entities has been realized. This review provides the background and current research in this area with emphasis of these agents as potential anticonvulsants, their proposed mechanisms of action, and as potential modulators of multidrug resistance (MDR).


Asunto(s)
Miembro 1 de la Subfamilia B de Casetes de Unión a ATP/antagonistas & inhibidores , Aminas/farmacología , Anticonvulsivantes/farmacología , Resistencia a Múltiples Medicamentos/efectos de los fármacos , Epilepsia/tratamiento farmacológico , Neuronas/efectos de los fármacos , Transmisión Sináptica/efectos de los fármacos , Miembro 1 de la Subfamilia B de Casetes de Unión a ATP/genética , Miembro 1 de la Subfamilia B de Casetes de Unión a ATP/metabolismo , Aminas/síntesis química , Aminas/metabolismo , Aminas/uso terapéutico , Animales , Anticonvulsivantes/síntesis química , Anticonvulsivantes/metabolismo , Anticonvulsivantes/uso terapéutico , Barrera Hematoencefálica/metabolismo , Cristalografía por Rayos X , Resistencia a Múltiples Medicamentos/genética , Epilepsia/genética , Epilepsia/metabolismo , Potenciales Postsinápticos Excitadores/efectos de los fármacos , Humanos , Modelos Químicos , Estructura Molecular , Neuronas/metabolismo , Polimorfismo de Nucleótido Simple , Relación Estructura-Actividad Cuantitativa , Ácido gamma-Aminobutírico/metabolismo
11.
Med Chem ; 1(4): 371-81, 2005 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16789894

RESUMEN

The enaminones represent potentially useful agents for the clinical treatment in generalized tonic-clonic seizures (Epilepsia, 1993, 34(6), 1141-1145, Biopharm. Drug Disp. 2003, 397-407). A regression analysis was performed to provide a quantitative structure-activity relationship (QSAR) correlation model for prediction of activity for the anticonvulsant enaminones. Molecular modeling was performed to determine the molecular confluence of the Unverferth model (J. Med. Chem. 1998, 41, 63-73) to the enaminones. Conclusions related to the sodium channel model were assessed.


Asunto(s)
Anticonvulsivantes/química , Cetonas/química , Modelos Biológicos , Pirroles/química , Relación Estructura-Actividad Cuantitativa , Bloqueadores de los Canales de Sodio/química , Animales , Cetonas/farmacología , Masculino , Ratones , Modelos Moleculares , Estructura Molecular , Análisis de Regresión
12.
Curr Med Chem ; 11(15): 2093-113, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15279569

RESUMEN

The multidrug resistance (MDR), often conferred by the active extrusion of drugs from the cell, is a phenomenon often seen in cancer cells that may become resistant to a wide spectrum of drugs with varying chemical structures or cellular targets. This event has recently been reported for anticonvulsants. Studies in our laboratories on this occurrence with some enaminones have shown that the enaminones display high efflux ratios and are recognized by P-glycoprotein (P-gp) and/or the multidrug resistance protein (MRP), which have been reported as the main efflux transporters responsible for the development of MDR. Recent studies have uncovered interesting structural analogues that can modulate the functional activity of P-gp, suggesting a possible increase in the bioavailabillity of P-gp substrate drugs when administered concurrently.


Asunto(s)
Miembro 1 de la Subfamilia B de Casetes de Unión a ATP/fisiología , Anticonvulsivantes/uso terapéutico , Ciclohexanonas/uso terapéutico , Resistencia a Múltiples Medicamentos , Animales , Encéfalo/metabolismo , Humanos , Proteínas Asociadas a Resistencia a Múltiples Medicamentos/fisiología
13.
Curr Med Chem ; 7(4): 417-36, 2000 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-10702617

RESUMEN

Enaminones, enamines of ss-dicarbonyl compounds, have been know for many years. In our initial account (Current Med. Chem. 1994, 1, 159-175), we reported on the anticonvulsant activity of a series of enaminones, notably methyl 4-[(p-chlorophenyl)amino]-6-methyl-2-oxo-cyclohex-3-en- 1-oate, 9a (R=CH3, R1=4-Cl), which, in animal tests, compared favorably to phenytoin and carbamazepine. Since that time, further research in our laboratory and other laboratories have expanded the therapeutic potential of these compounds. In addition to new anticonvulsant derivatives, we have uncovered a novel brain transport mechanism for the enaminones and developed a preliminary regression model for further synthetic direction. These topics will each be presented and elaborated.


Asunto(s)
Aminas/química , Anticonvulsivantes/química , Animales , Anticonvulsivantes/síntesis química , Humanos
14.
J Med Chem ; 34(1): 387-92, 1991 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-1992141

RESUMEN

Previous results of anticonvulsant activity in several imidooxy carboxylates related to (aminooxy)acetic acid in young chicks, prompted an in-depth reinvestigation of these analogues in mice. A series of 22 succinimidooxy, phthalimidooxy, and naphthalimidooxy carboxylates were synthesized and evaluated for anticonvulsant activity by the National Institute of Neurological and Communicative Disorders and Stroke (NINCDS). Methyl (succinimidooxy)acetate (2d), ethyl (succinimidooxy)acetate (2e), methyl (phthalimidooxy)acetate (3d), ethyl (phthalimidooxy)acetate (3e), and ethyl 2-(phthalimidooxy)propionate (3g), which were initially found to be active as anticonvulsants in young chicks were uniformly inactive in the Phase I seizure tests involving maximal electroshock (MES), pentylenetetrazol (scMet), or neurologic toxicity toxicity (Tox). Several newer analogues, ethyl (succinimidooxy)formate (2c) and methyl 3-(phthalimidooxy)-2-methylacrylate (4h) were found to be active in the scMet (3a) or both (4h) evaluations. Most interesting was the anticonvulsant results of N-(benzyloxy)-2-azaspiro[4,4] nonane-1,3-dione (5b), which displayed anti-MES activity and a protective index (TD50/ED50) of greater than 4.5.


Asunto(s)
Anticonvulsivantes/síntesis química , Imidas/síntesis química , Animales , Pollos , Electrochoque , Imidas/farmacología , Imidas/toxicidad , Indicadores y Reactivos , Estructura Molecular , Ftalimidas/síntesis química , Ftalimidas/farmacología , Ftalimidas/toxicidad , Reflejo/efectos de los fármacos , Relación Estructura-Actividad , Succinimidas/síntesis química , Succinimidas/farmacología , Succinimidas/toxicidad
15.
J Med Chem ; 35(15): 2798-805, 1992 Jul 24.
Artículo en Inglés | MEDLINE | ID: mdl-1495012

RESUMEN

A new series of novel enaminones has been synthesized from cyclic beta-dicarbonyl precursors which were condensed with morpholine, pyrrolidine, phenethylamine, hydrazines, substituted benzyl amines, and substituted anilines. These compounds were subsequently evaluated for anticonvulsant activity in a variety of anticonvulsant models by the National Institute of Neurological and Communicative Disorders and Stroke and in our laboratory. Several of these compounds exhibited potent anticonvulsant activity with a remarkable lack of neurotoxicity. The most active analog, methyl 4-[(p-chlorophenyl)amino]-6-methyl-2-oxo-cyclohex-3-en-1-oate++ + (27), was protective in the maximal electroshock (MES) seizure test in the rat with an oral ED50 of 5.8 mg/kg with no toxicity noted at doses up to 380 mg/kg, thus providing a protective index (TD50/ED50) of greater than 65.5. A similar protective index for 27 was noted upon intraperitoneal (ip) administration in mice. The anticonvulsant effect of 27 occurred within 15 min of administration and the compound remained active beyond 4 h. Compound 27 was also active in the rat corneal kindled model. The application of Free-Wilson analysis to structure-activity correlation in this series is discussed.


Asunto(s)
Aminas/farmacología , Anticonvulsivantes/farmacología , Aminas/síntesis química , Animales , Anticonvulsivantes/síntesis química , Evaluación Preclínica de Medicamentos , Estimulación Eléctrica , Excitación Neurológica , Masculino , Ratones , Ratas , Convulsiones/etiología , Relación Estructura-Actividad
16.
J Med Chem ; 28(4): 413-7, 1985 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-3920394

RESUMEN

Spiro[4.5]decane-2-carboxylic acid (12a), spiro[4.5]decane-2,2-dicarboxylic acid (11a), spiro[4.6]undecane-2-carboxylic acid (12b), spiro[4.6]undecane- 2,2-dicarboxylic acid (11b), and spiro[4.6]undecane-2-acetic acid (13) were synthesized by an improved method and evaluated for anticonvulsant activity. These analogues were synthesized to evaluate the role of the carboxylic acid group as an essential substituent in valproic acid (di-n-propylacetic acid, 1). Carbocyclic spiranes are known to resist metabolic alteration so that any activity elicited by these compounds would be due to the carboxylic acid function and not to any metabolic change. Spiro[4.6]undecane-2-carboxylic acid (12b) was the most active analogue tested and the pentylenetetrazol and picrotoxin evaluations of 12b compared favorably to 1. However, 12b failed to provide adequate protection against maximal electroshock seizures, bicuculline, or strychnine in mice. Possible reasons for these results are discussed.


Asunto(s)
Anticonvulsivantes/síntesis química , Compuestos de Espiro/síntesis química , Ácido Valproico/análogos & derivados , Animales , Anticonvulsivantes/farmacología , Bicuculina , Ácidos Carboxílicos/síntesis química , Ácidos Carboxílicos/farmacología , Masculino , Ratones , Pentilenotetrazol , Picrotoxina , Compuestos de Espiro/farmacología , Relación Estructura-Actividad , Ácido Valproico/metabolismo
17.
J Med Chem ; 36(14): 1947-55, 1993 Jul 09.
Artículo en Inglés | MEDLINE | ID: mdl-8336334

RESUMEN

This report continues the in-depth evaluation of methyl 4-[(p-chlorophenyl)amino]-6-methyl-2-oxocyclohex-3-en-1-oate , 1 (ADD 196022), and methyl 4-(benzylamino)-6-methyl-2-oxocyclohex-3-en-1-oate, 2, two potent anticonvulsant enaminones. These compounds were evaluated employing the amygdala kindling model. Neither 1 nor 2 was active against amygdala kindled seizures, further supporting the corneal kindled model as a definitive tool for antielectroshock seizure evaluation as previously reported. Additional intraperitoneal (ip) data on 1 revealed toxicity at 24 h at 100 mg/kg. Several active analogs have been prepared with the view to minimizing toxicity. In a special ip rat screen developed by the Antiepileptic Drug Development (ADD) Program, these newer analogs were evaluated for protection against maximal electroshock seizures (MES) at 10 mg/kg and neurotoxicity at 100 mg/kg. From this screen, several compounds were shown to be safer alternatives, the most notable was methyl 4-[(p-bromophenyl)amino]-6-methyl-2-oxocyclohex-3-en-1-oate, 13. Compound 13 had an ip ED50 of 4 mg/kg in the rat and a TD50 of 269 mg/kg, providing a protective index (TD50/ED50) of > 67. By variation in the ring size, additional aromatic substitutions and the synthesis of acyclic analogs, these newer compounds provide a more definitive insight into the structure-activity correlation. CLOGP evaluation and molecular modeling studies are also provided to further elaborate the molecular characteristics of potential anticonvulsant enaminones.


Asunto(s)
Anticonvulsivantes/síntesis química , Anticonvulsivantes/farmacología , Bencilaminas/síntesis química , Ácidos Ciclohexanocarboxílicos/síntesis química , Ciclohexilaminas , Convulsiones/tratamiento farmacológico , Animales , Anticonvulsivantes/química , Bencilaminas/química , Bencilaminas/farmacología , Ácidos Ciclohexanocarboxílicos/química , Ácidos Ciclohexanocarboxílicos/farmacología , Excitación Neurológica/efectos de los fármacos , Masculino , Ratones , Modelos Moleculares , Ratas , Ratas Sprague-Dawley , Relación Estructura-Actividad
18.
J Med Chem ; 38(20): 4033-43, 1995 Sep 29.
Artículo en Inglés | MEDLINE | ID: mdl-7562939

RESUMEN

In a continuing evaluation of the aniline-substituted enaminones, the synthesis of additional para-substituted analogs has been made in an attempt to further quantify the electronic (sigma) and lipophilic (pi) requirements for anticonvulsant activity in this series. In addition, meta- and ortho-substituted and polysubstituted compounds have been synthesized and evaluated for anticonvulsant activity. In the para-substituted series, 4-cyano analogs (32 and 33) (+ sigma, - pi), which were highly active via intraperitoneal (ip) injection in mice, were inactive on oral (po) administration in rats. The para-substituted trifluoromethoxy (+ sigma, + pi) analog (8) had significant potency by both routes. Meta substitution limited the activity due to steric factors. Bromo and iodo substituents produced active para-substituted analogs (5 and 17) but were inactive when substituted in the meta position (37 and 41, respectively). Ortho substitution provided no clear relationship due to nonparametric deviations. Neither 1, the prototype enaminone, nor 2, the putative metabolite, produced significant nephrotoxicity or hepatotoxicity. Sodium channel binding of 1 and 8 indicated that 8 displayed relatively potent sodium channel binding but 1 showed weaker effects with IC50 values of 489 and 170 microM respectively against [3H]batrachotoxinin A 20 alpha-benzoate ([3H]BTX-B).


Asunto(s)
Anticonvulsivantes/síntesis química , Canales de Sodio/efectos de los fármacos , Animales , Anticonvulsivantes/farmacología , Anticonvulsivantes/toxicidad , Batracotoxinas/metabolismo , Riñón/efectos de los fármacos , Hígado/efectos de los fármacos , Masculino , Ratones , Ratas , Ratas Endogámicas F344 , Canales de Sodio/metabolismo , Relación Estructura-Actividad
19.
Eur J Pharm Biopharm ; 52(2): 145-50, 2001 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11522479

RESUMEN

Zonula occludens toxin (Zot), a protein elaborated from Vibrio cholerae, has been shown to be capable of reversibly opening tight junctions between intestinal cells The objective of this study was to examine the effect of Zot on the flux of various molecules across Caco-2 cell monolayers. In addition, the transport of a series of anticonvulsants, the enaminones was also evaluated in the presence of Zot. The flux of [(14)C]mannitol, [(14)C]inulin and various enaminones across Caco-2 cell monolayers (n=6) was examined after pre-incubation for 1h with Zot (0 or 4000ng/ml) or phosphate-buffered saline (PBS). At the end of the incubation period, the flux of radiolabeled compounds or enaminones (1x10(-4)M) was assessed over a 2-h period. In addition, dose-response studies with Zot (0, 1000, 2000 or 4000ng/ml) were performed using mannitol. The flux of both mannitol and inulin significantly increased (P<0.05) in the presence of Zot. The transport of the enaminones with Zot ranged from 9.42 to 26.83x10(-5)cm/s vs. 4.68 to 13.83x10(-5)cm/s without Zot. Zot significantly increased the transport of all agents tested. This suggests that the co-administration of drugs with Zot may be a useful delivery strategy to increase the intestinal permeability and hence oral absorption of poorly bioavailable agents.


Asunto(s)
Anticonvulsivantes/farmacocinética , Células CACO-2/metabolismo , Toxina del Cólera/farmacocinética , Uniones Estrechas/metabolismo , Anticonvulsivantes/administración & dosificación , Anticonvulsivantes/química , Técnicas de Cultivo de Célula/métodos , Toxina del Cólera/administración & dosificación , Diuréticos Osmóticos/administración & dosificación , Diuréticos Osmóticos/farmacocinética , Endotoxinas , Humanos , Absorción Intestinal/efectos de los fármacos , Absorción Intestinal/fisiología , Inulina/administración & dosificación , Inulina/farmacocinética , Manitol/administración & dosificación , Manitol/farmacocinética , Peso Molecular , Uniones Estrechas/efectos de los fármacos
20.
J Pharm Sci ; 74(7): 785-7, 1985 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-4032256

RESUMEN

A series of spirosuccinimides was synthesized and evaluated for anticonvulsant activity. The study was designed to apply the Topliss approach to structure-activity correlations in this novel series of 2-substituted-2-azaspiro[4.4]nonane-1,3-diones and 2,4-disubstituted-2-azaspiro[4.4]nonane-1,3-diones. While no correlation was noted with the 2-substituted derivatives, a good correlation was obtained in the 2,4-disubstituted series, indicating that anticonvulsant activity was related to increasing tau values. The results of these anticonvulsant tests are presented and a rational approach to the structure-activity relationships of spirosuccinimides is provided.


Asunto(s)
Anticonvulsivantes/síntesis química , Succinimidas/síntesis química , Animales , Fenómenos Químicos , Química , Electrochoque , Masculino , Ratones , Pentilenotetrazol/antagonistas & inhibidores , Succinimidas/farmacología
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