RESUMO
CONTEXT: The bulb of Allium sativum Linn (Alliaceae) has numerous medicinal values. Though the petroleum ether extract of the bulb has shown to exhibit antimycobacterial activity, the phytochemical(s) responsible for this inhibitory activity is not known. OBJECTIVE: To characterize the bioactive compounds in the petroleum ether extract of Allium sativum (garlic) that inhibit the growth of Mycobacterium tuberculosis H37Ra. MATERIALS AND METHODS: Bioactivity-guided fractionation was employed to isolate the bioactive compounds. Antimycobacterial activity was evaluated by well-diffusion method and microplate alamar blue assay (MABA). Infrared spectroscopy, mass spectrometry and nuclear magnetic resonance spectroscopy were used to characterize the bioactive compounds. Autodock was used to obtain information on molecular recognition, and molecular dynamics simulation was performed using GROMACS. RESULTS: The bioactive compounds that inhibited the growth of M. tuberculosis H37Ra were found to be lauric acid (LA) and myristic acid (MA). The minimal inhibitory concentration of LA and MA was found to be 22.2 and 66.7 µg/mL, respectively. In silico analysis revealed that these fatty acids could bind at the cleft between the N-terminal and C-terminal lobes of the cytosolic domain of serine/threonine protein kinase B (PknB). DISCUSSION AND CONCLUSION: The inhibition activity was dependent on the alkyl chain length of the fatty acid, and the amino acid residues involved in binding to fatty acid was found to be conserved across the Pkn family of proteins. The study indicates the possibility of using fatty acid derivatives, involving Pkn family of proteins, to inhibit the signal transduction processes in M. tuberculosis.
Assuntos
Alho , Ácidos Láuricos/metabolismo , Mycobacterium tuberculosis/metabolismo , Ácido Mirístico/metabolismo , Extratos Vegetais/metabolismo , Proteínas Proto-Oncogênicas c-akt/metabolismo , Antituberculosos/isolamento & purificação , Antituberculosos/metabolismo , Antituberculosos/farmacologia , Simulação por Computador , Humanos , Ácidos Láuricos/isolamento & purificação , Ácidos Láuricos/farmacologia , Mycobacterium tuberculosis/efeitos dos fármacos , Mycobacterium tuberculosis/crescimento & desenvolvimento , Ácido Mirístico/isolamento & purificação , Ácido Mirístico/farmacologia , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Raízes de Plantas , Ligação Proteica/fisiologia , Estrutura Secundária de Proteína , Estrutura Terciária de Proteína , Proteínas Proto-Oncogênicas c-akt/químicaRESUMO
Nowadays, data concerning the composition of Caryodendron orinocense Karst. (Euphorbiaceae) and Bactris gasipaes Kunth (Arecaceae) seed oils are lacking. In light of this fact, in this paper fatty acids and unsaponifiable fraction composition have been determined using GC-MS, HPLC-DAD (Diode Array Detector), NMR approaches and possible future applications have been preliminary investigated through estimation of antioxidant activity, performed with DPPH test. For C. orinocense linoleic acid (85.59%) was the main component, lauric (33.29%) and myristic (27.76%) acids were instead the most abundant in B. gasipaes. C. orinocense unsaponifiable fraction (8.06%) evidenced a remarkable content of ß-sitosterol, campesterol, stigmasterol, squalene and vitamin E (816 ppm). B. gasipaes revealed instead ß-sitosterol and squalene as main constituents of unsaponifiable matter (3.01%). Antioxidant capacity evidenced the best performance of C. orinocense seed oil. These preliminary results could be interesting to suggest the improvement of the population's incomes from Amazonian basin. In particular the knowledge of chemical composition of C. orinocense and B. gasipaes oils could be helpful to divulge and valorize these autochthones plants.
Assuntos
Antioxidantes , Arecaceae/química , Euphorbiaceae/química , Ácidos Graxos/isolamento & purificação , Ácidos Graxos/farmacologia , Nozes/química , Óleos de Plantas/química , Sementes/química , Colesterol/análogos & derivados , Colesterol/análise , Colesterol/isolamento & purificação , Colesterol/farmacologia , Cromatografia Líquida de Alta Pressão , Ácidos Graxos/análise , Sequestradores de Radicais Livres , Cromatografia Gasosa-Espectrometria de Massas , Ácidos Láuricos/análise , Ácidos Láuricos/isolamento & purificação , Ácidos Láuricos/farmacologia , Ácido Linoleico/análise , Ácido Linoleico/isolamento & purificação , Ácido Linoleico/farmacologia , Espectroscopia de Ressonância Magnética , Ácido Mirístico/análise , Ácido Mirístico/isolamento & purificação , Ácido Mirístico/farmacologia , Fitosteróis/análise , Fitosteróis/isolamento & purificação , Fitosteróis/farmacologia , Óleos de Plantas/isolamento & purificação , Sitosteroides/análise , Sitosteroides/isolamento & purificação , Sitosteroides/farmacologia , Esqualeno/análise , Esqualeno/isolamento & purificação , Esqualeno/farmacologia , Estigmasterol/análise , Estigmasterol/isolamento & purificação , Estigmasterol/farmacologia , Vitamina E/análise , Vitamina E/isolamento & purificação , Vitamina E/farmacologiaRESUMO
A new alkylamine derivative and a common fatty acid were isolated from Streptomyces sp. YIM 66142. On the basis of spectral data, including HRMS, NMR and 2D NMR, their structures were determined as medelamine C (1) and isomyristic acid (2). The omega-hydroxyl group in structure 1 is rare in a natural alkylamine. The possible biosynthetic pathway in the genus Streptomyces from isomyristic acid (2) to medelamines is proposed. Compound 1 showed no obvious cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, SW480 cell lines. The omega-hydroxyl and the acetyl at NH in compound 1 decreased its cytotoxicity in comparison with that of medelamine.
Assuntos
Ácidos Graxos/isolamento & purificação , Ácido Mirístico/isolamento & purificação , Streptomyces/química , Ensaios de Seleção de Medicamentos Antitumorais , Endófitos/química , Células HL-60 , Humanos , Células MCF-7 , Ácido Mirístico/químicaRESUMO
Malaria is an overwhelming impact in the poorest countries in the world due to their prevalence, virulence and drug resistance ability. Currently, there is inadequate armoury of drugs for the treatment of malaria. This underscores the continuing need for the discovery and development of new effective and safe antimalarial drugs. To evaluate the in vitro and in vivo antimalarial activity of the leaf ethyl acetate extract of Murraya koenigii, bioassay-guided chromatographic fractionation was employed for the isolation and purification of antimalarial compounds. The in vitro antimalarial activity was assayed by the erythrocytic stages of chloroquine-sensitive strain of Plasmodium falciparum (3D7) in culture using the fluorescence-based SYBR Green I assay. The in vivo assay was done by administering mice infected with Plasmodium berghei (NK65) four consecutive daily doses of the extracts through oral route following Peter's 4-day curative standard test. The percentage suppression of parasitaemia was calculated for each dose level by comparing the parasitaemia in untreated control with those of treated mice. Cytotoxicity was determined against HeLa cells using MTT assay. Histopathology was studied in kidney, liver and spleen of isolated compound-treated Swiss albino mice. The leaf crude ethyl acetate extract of M. koenigii showed good in vitro antiplasmodial activity against P. falciparum. The in vivo test of the leaf crude ethyl acetate extract (600 mg/kg) showed reduced malaria parasitaemia by 86.6% against P. berghei in mice. Bioassay-guided fractionation of the leaf ethyl acetate extract of M. koenigii led to the isolation of two purified fractions C3B2 (2.84 g) and C3B4 (1.97 g). The purified fractions C3B2 and C3B4 were found to be active with IC50 values of 10.5 ± 0.8 and 8.25 ± 0.2 µg/mL against P. falciparum, and in vivo activity significantly reduced parasitaemia by 82.6 and 88.2% at 100 mg/kg/body weight on day 4 against P. berghei, respectively. The isolated fractions C3B2 and C3B4 were monitored by thin-layer chromatography until a single spot was obtained with R f values of 0.36 and 0.52, respectively. The pure compounds obtained in the present investigation were subjected to UV-visible spectroscopy, Fourier transformer infrared spectroscopy, 1D and 2D (1)H-Nuclear magnetic resonance (NMR), (13)C NMR, DEPT, COSY and Mass spectral analysis. Based on the spectral analysis, it is concluded that the isolated compounds were myristic acid (C3B2) and ß-caryophyllene (C3B4). The cytotoxic effect of myristic acid and ß-caryophyllene showed the TC50 values of >100 and 80.5 µg/mL, respectively against HeLa cell line. The histopathology study showed that protection against nephrotoxicity of kidney, hepatic damage of liver and splenocytes protection in spleen was achieved with the highest dose tested at 100 mg/kg/body weight. The present study provides evidence of antiplasmodial compounds from M. koenigii and is reported for the first time.
Assuntos
Antimaláricos/farmacologia , Murraya/química , Extratos Vegetais/farmacologia , Plasmodium berghei/efeitos dos fármacos , Plasmodium falciparum/efeitos dos fármacos , Animais , Antimaláricos/química , Feminino , Células HeLa , Humanos , Malária/tratamento farmacológico , Masculino , Camundongos , Ácido Mirístico/isolamento & purificação , Extratos Vegetais/química , Folhas de Planta/química , Sesquiterpenos Policíclicos , Sesquiterpenos/isolamento & purificaçãoRESUMO
D-004, a lipid extract of Roystonea regia fruits that contains oleic, lauric and myristic acids as major components inhibits alpha1-adrenoreceptors-mediated contractile responses in isolated rat vas deferens and prostate trips; no study has demonstrated a similar effect for oleic, lauric or myristic acids individually. Therefore, the effects of D-004 (250 microg/mL), oleic (100 microg/mL), lauric (50 microg/mL) or myristic (25 microg/mL) acids and their combined effects on phenylephrine (PHE: 10(-7)-10(-4) mol/L) induced contractions has been studied. No treatment changed the basal tone of the preparations, but all inhibited PHE-induced contractions. D-004 produced the highest inhibition, followed by lauric acid, which was more effective than myristic and oleic acids against PHE-induced contractions of control group. D-004 and the mixture of the three acids produced similar inhibitions.
Assuntos
Antagonistas de Receptores Adrenérgicos alfa 1/farmacologia , Ácidos Láuricos/farmacologia , Contração Muscular/efeitos dos fármacos , Ácido Mirístico/farmacologia , Ácido Oleico/farmacologia , Ducto Deferente/efeitos dos fármacos , Antagonistas de Receptores Adrenérgicos alfa 1/isolamento & purificação , Animais , Arecaceae , Técnicas In Vitro , Ácidos Láuricos/isolamento & purificação , Masculino , Músculo Liso/efeitos dos fármacos , Ácido Mirístico/isolamento & purificação , Ácido Oleico/isolamento & purificação , Fenilefrina/farmacologia , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Hiperplasia Prostática/tratamento farmacológico , Hiperplasia Prostática/metabolismo , Hiperplasia Prostática/fisiopatologia , Ratos , Ratos Sprague-Dawley , Ducto Deferente/metabolismoRESUMO
OBJECTIVE: To investigate the chemical constituents of Ardisia tenera Mez. METHODS: Compounds were isolated by normal phase silica gel, MCI GEL and Sephadex LH-20 gel column chromatography. Their structures were elucidated by analyses of spectroscopic data. RESULTS: Eight compounds were isolated, and their structures were elucidated as bauerenol (I), myristic acid (II), 11-phenyl-1-(2',6'-dihydroxy-4'-methoxy-phenyl)-undecan-1 -one (III), ardisinone A( IV), ardisinone B( V ), ardisinone C( VI), ardisinone F (VI), beta-sitosterol (VIII). CONCLUSION: All of these compounds are obtained from this plant for the first time.
Assuntos
Ardisia/química , Extratos Vegetais/química , Plantas Medicinais/química , Etanol/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Ácido Mirístico/química , Ácido Mirístico/isolamento & purificação , Componentes Aéreos da Planta/química , Extratos Vegetais/isolamento & purificaçãoRESUMO
OBJECTIVE: To analyze and identify fatty acids from the flowers of Trollius chinensis Bunge. METHODS: To isolate and determine the constituents using GC/MS technique, quantitatively analyze their content by area normalization method. RESULTS: 31 fatty acids and 7 other constituents were isolated and determined. CONCLUSION: The major fatty acids were hexadecanoic (19.85%), (Z,Z)-9,12-octadecadienoic (14.37%), tetradecanoic (13.93%), (Z)-9-octadecenoic (13.00%), dodecanoic (6.79%), 10-hydroxy-hexadecanoic (4.37%) and octadecanoic (3.34%) acids.
Assuntos
Ácidos Graxos/análise , Flores/química , Plantas Medicinais/química , Ranunculaceae/química , Ácidos Graxos/química , Ácidos Graxos/isolamento & purificação , Cromatografia Gasosa-Espectrometria de Massas , Ácidos Láuricos/análise , Ácidos Láuricos/química , Ácidos Láuricos/isolamento & purificação , Estrutura Molecular , Peso Molecular , Ácido Mirístico/análise , Ácido Mirístico/química , Ácido Mirístico/isolamento & purificação , Ácido Palmítico/análise , Ácido Palmítico/química , Ácido Palmítico/isolamento & purificação , Ácidos Esteáricos/análise , Ácidos Esteáricos/química , Ácidos Esteáricos/isolamento & purificaçãoRESUMO
Nutmeg (Myristica fragrans) is used in food preparations for its aromatic flavor. The present investigation was undertaken to evaluate the antibacterial activity of constituents of M. fragrans seeds. Seeds of M. fragrans were powdered and extracted with chloroform to obtain trimyristin, which on saponification yielded myristic acid. The mother liquor remaining after separation of trimyristin was concentrated and column-chromatographed with petroleum ether to separate myristicin. Antibacterial activity of these isolated constituents was evaluated by determination of minimum inhibitory concentration against selected Gram-positive and Gram-negative organisms. All the constituents isolated from nutmeg exhibited good antibacterial activity. This study shows the potential of natural compounds in replacement of synthetic preservatives.
Assuntos
Antibacterianos/isolamento & purificação , Myristica/química , Sementes/química , Derivados de Alilbenzenos , Antibacterianos/farmacologia , Compostos de Benzil/isolamento & purificação , Compostos de Benzil/farmacologia , Clorofórmio , Dioxolanos/isolamento & purificação , Dioxolanos/farmacologia , Bactérias Gram-Negativas/efeitos dos fármacos , Bactérias Gram-Positivas/efeitos dos fármacos , Ácido Mirístico/isolamento & purificação , Ácido Mirístico/farmacologia , Extratos Vegetais/química , Pirogalol/análogos & derivados , Pirogalol/isolamento & purificação , Pirogalol/farmacologia , Triglicerídeos/isolamento & purificação , Triglicerídeos/farmacologiaRESUMO
O fracionamento cromatográfico do extrato hexânico das partes aéreas de Cambessedesia espora DC - Melastomataceae levou ao isolamento dos ácidos palmítico, mirístico e esteárico, ß-Silosterol e do triterpeno fern-9(11)-en-3ß-ol. As substâncias foram identificadas por métodos espectroscópicos usuais (RMN, IV, CG/EM).