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1.
Bioorg Chem ; 96: 103626, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32007719

RESUMEN

We, herein, describe the synthesis of a series of novel aryl tethered 7,8-dihydroquinolin-5(6H)-ylidenehydrazinecarbothioamides 4a-v, which showed in vitro and in vivo antimycobacterial activity against Mycobacterium tuberculosis (Mtb) H37Rv. The intermediates dihydro-6H-quinolin-5-ones 3a-v were synthesized from ß-enaminones, reacting with cyclochexane-1,3-dione/5,5-dimethylcyclohexane-1,3-dione and ammonium acetate using a modified Bohlmann-Rahtz reaction conditions. They were further reacted with thiosemicarbazide to give the respective hydrazine carbothioamides 4a-v. All the new analogues 4a-v, were characterized by their NMR and mass spectral data analysis. Among the twenty-two compounds screened for in vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv (ATCC27294), two compounds, 4e and 4j, exhibited the highest inhibition with an MIC of 0.39 µg/mL. Compounds 4a, 4g, and 4k were found to inhibit Mtb at an MIC of 0.78 µg/mL. Hydrazinecarbothioamides 4a-k, exhibited enhanced activity than dihydroquinolinones 3a-k. The observed increase in potency provides a clear evidence that hydrazinecarbothioamide is a potential pharmacophore, collectively imparting synergistic effect in enhancing antitubercular activity of the dihydroquinolinone core. The in vivo (Zebra fish) antimycobacterial screening of the in vitro active molecules led to the identification of a hit compound, 4j, with significant activity in the Mtb nutrient starvation model (2.2-fold reduction). Docking studies of 4j showed a hydrogen bond with the P156 residue of the protein.


Asunto(s)
Antituberculosos/química , Antituberculosos/uso terapéutico , Hidrazinas/química , Hidrazinas/uso terapéutico , Mycobacterium tuberculosis/efectos de los fármacos , Tioamidas/química , Tioamidas/uso terapéutico , Tuberculosis/tratamiento farmacológico , Animales , Antituberculosos/síntesis química , Modelos Animales de Enfermedad , Diseño de Fármacos , Humanos , Hidrazinas/síntesis química , Pruebas de Sensibilidad Microbiana , Simulación del Acoplamiento Molecular , Quinolonas/síntesis química , Quinolonas/química , Quinolonas/uso terapéutico , Relación Estructura-Actividad , Tioamidas/síntesis química , Pez Cebra
2.
Endocrinol Nutr ; 58(3): 121-6, 2011 Mar.
Artículo en Español | MEDLINE | ID: mdl-21367680

RESUMEN

INTRODUCTION: Amiodarone-induced thyrotoxicosis (AIT) is a common clinical disorder that may be life threatening and whose clinical manifestations and response to treatment may vary among patients. METHODS: We present three patients treated with amiodarone for atrial fibrillation who developed AIT at least 36 months after beginning the treatment. Thyrotoxicosis worsened the underlying cardiac disorders and was resistant to treatment based on the combination of dexamethasone 8-12 mg/day i.v., thioamides 45 mg/day p.o., beta blockers and potassium perchlorate at doses of 800 to 1000 mg per day p.o. Two of the patients attained sustained euthyroidism after 12 and 32 days of combined treatment, while the third required total thyroidectomy. CONCLUSION: The combination of thioamides with potassium perchlorate is an appropriate form of therapy for AIT in patients resistant to thioamides. The use of this combination should be evaluated in patients with mixed AIT or AIT of unclear etiology.


Asunto(s)
Amiodarona/efectos adversos , Percloratos/uso terapéutico , Compuestos de Potasio/uso terapéutico , Tirotoxicosis/tratamiento farmacológico , Acenocumarol/administración & dosificación , Acenocumarol/uso terapéutico , Antagonistas Adrenérgicos beta/administración & dosificación , Antagonistas Adrenérgicos beta/uso terapéutico , Anciano , Anciano de 80 o más Años , Algoritmos , Amiodarona/uso terapéutico , Fibrilación Atrial/tratamiento farmacológico , Fármacos Cardiovasculares/uso terapéutico , Comorbilidad , Dexametasona/administración & dosificación , Dexametasona/uso terapéutico , Quimioterapia Combinada , Femenino , Humanos , Masculino , Persona de Mediana Edad , Marcapaso Artificial , Percloratos/administración & dosificación , Compuestos de Potasio/administración & dosificación , Tioamidas/administración & dosificación , Tioamidas/uso terapéutico , Hormonas Tiroideas/sangre , Tiroidectomía , Tirotoxicosis/sangre , Tirotoxicosis/inducido químicamente , Tirotoxicosis/cirugía , Tirotropina/sangre
3.
Indian J Tuberc ; 55(1): 15-21, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18361306

RESUMEN

AIM: To determine the clinical, radiological and drug resistance profile as well as the factors associated with treatment outcome of Multi-Drug Resistant Tuberculosis (MDR-TB). MATERIAL AND METHODS: All newly diagnosed patients with pulmonary MDR-TB from August 2002 to December 2004 enrolled at New Delhi Tuberculosis Centre, were included in the study. They were followed up clinically, radiologically and bacteriologically by sputum smear, culture and Drug Susceptibility Testing (DST) at regular intervals. According to their DST pattern and previous history of Anti-Tubercular Treatment (ATT), individualized treatment regimens were tailored for each patient. RESULTS: Out of total 27 bacteriologically proven cases of MDR-TB included in this study, 19 were males (mean age and weight 38.5 years and 52.6 kgs, respectively) and eight females (mean age and weight 34.3 years and 40.7 kgs, respectively). A majority (18) were residents of Delhi and the rest hailed from different parts of North India. All of them had a history of previous treatment ranging from six to 34 months. Cavity on chest X-rays was seen in 81%, while 44% showed extensive involvement. The patients received at least four "second line drugs" during their treatment with a mean of 6.2 anti-tubercular drugs during their intensive phase. Of the 27 patients, 13 were cured, 10 defaulted, one died, one is still on treatment and two were referred for surgery. Radiological improvement was observed in two third of cases and chest X-ray of two patients showed a complete resolution. Six predictors were identified for successful outcome of MDR-TB. They include weight gain at six months, culture conversion, radiological improvement during treatment, disease with M. tuberculosis strains exhibiting resistance to less than or up to three anti-tubercular drugs, use of less than or up to three second line drugs in treatment and no change of regimen during treatment. CONCLUSION: Default from treatment was observed to be a major challenge in the treatment of MDR-TB due to long duration and expense of ATT.


Asunto(s)
Antituberculosos/uso terapéutico , Tuberculosis Resistente a Múltiples Medicamentos/tratamiento farmacológico , Adolescente , Adulto , Aminoglicósidos/administración & dosificación , Aminoglicósidos/uso terapéutico , Ácido Aminosalicílico/administración & dosificación , Ácido Aminosalicílico/uso terapéutico , Antituberculosos/administración & dosificación , Niño , Cicloserina/administración & dosificación , Cicloserina/uso terapéutico , Etambutol/administración & dosificación , Etambutol/uso terapéutico , Femenino , Fluoroquinolonas/administración & dosificación , Fluoroquinolonas/uso terapéutico , Estudios de Seguimiento , Humanos , Masculino , Pruebas de Sensibilidad Microbiana , Persona de Mediana Edad , Pirazinamida/administración & dosificación , Pirazinamida/uso terapéutico , Radiografía , Índice de Severidad de la Enfermedad , Tioamidas/administración & dosificación , Tioamidas/uso terapéutico , Factores de Tiempo , Resultado del Tratamiento , Tuberculosis Resistente a Múltiples Medicamentos/diagnóstico por imagen
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