RESUMEN
Marine natural products comprise unique chemical structures and vast varieties of biological activities. This review aims to summarize halichondrin, a marine natural product, and its synthetic analogs along with its therapeutic properties and mechanisms. Halichondrin and its analogs, derived from marine sponges, exhibit potent antineoplastic properties, making them promising candidates for cancer therapeutics. These compounds, characterized by their complex molecular structures, have demonstrated significant efficacy in inhibiting microtubule dynamics, leading to cell cycle arrest and apoptosis in various cancer cell lines. Several types of halichondrins such as halichondrins B, C, norhalichondrin B, and homohalichondrin B have been discovered with similar anticancer and antitumor characteristics. Since naturally available halichondrins show hurdles in synthesis, recent advancements in synthetic methodologies have enabled the development of several halichondrin analogs, such as E7389 (eribulin), which have shown improved therapeutic indices. Eribulin has shown excellent immunomodulatory properties by several mechanisms such as reprogramming tumor microenvironments, facilitating the infiltration and activation of immune cells, and inhibiting microtubule dynamics. Despite promising results, challenges remain in the synthesis and clinical application of these compounds. This review explores the mechanisms underlying the immunomodulatory activity of halichondrin and its analogs in cancer therapy, along with their clinical applications and potential for future drug development.
Asunto(s)
Antineoplásicos , Poríferos , Animales , Poríferos/química , Humanos , Antineoplásicos/farmacología , Antineoplásicos/química , Neoplasias/tratamiento farmacológico , Productos Biológicos/farmacología , Productos Biológicos/química , Furanos/farmacología , Furanos/química , Furanos/aislamiento & purificación , Organismos Acuáticos , Cetonas/farmacología , Cetonas/química , Cetonas/aislamiento & purificación , Factores Inmunológicos/farmacología , Factores Inmunológicos/química , Factores Inmunológicos/aislamiento & purificación , Agentes Inmunomoduladores/farmacología , Agentes Inmunomoduladores/química , Agentes Inmunomoduladores/aislamiento & purificación , Macrólidos/farmacología , Macrólidos/química , Policétidos Poliéteres , Éteres CíclicosRESUMEN
Invasive species events related to globalization are increasing, resulting in parasitic outbreaks. Understanding of host defense mechanisms is needed to predict and mitigate against the consequences of parasite invasion. Using the honey bee Apis mellifera and the mite Varroa destructor, as a host-parasite model, we provide a comprehensive study of a mechanism of parasite detection that triggers a behavioral defense associated with social immunity. Six Varroa-parasitization-specific (VPS) compounds are identified that (1) trigger Varroa-sensitive hygiene (VSH, bees' key defense against Varroa sp.), (2) enable the selective recognition of a parasitized brood and (3) induce responses that mimic intrinsic VSH activity in bee colonies. We also show that individuals engaged in VSH exhibit a unique ability to discriminate VPS compounds from healthy brood signals. These findings enhance our understanding of a critical mechanism of host defense against parasites, and have the potential to apply the integration of pest management in the beekeeping sector.
Asunto(s)
Acetatos/aislamiento & purificación , Abejas/metabolismo , Conducta Animal/fisiología , Mezclas Complejas/química , Cetonas/aislamiento & purificación , Varroidae/química , Acetatos/química , Acetatos/farmacología , Animales , Abejas/citología , Abejas/efectos de los fármacos , Abejas/parasitología , Conducta Animal/efectos de los fármacos , Bioensayo , Mezclas Complejas/farmacología , Femenino , Interacciones Huésped-Parásitos , Cetonas/química , Cetonas/farmacología , Varroidae/patogenicidadRESUMEN
Antimicrobial compounds from the safest source have gained greater relevance because of their wide spectrum of possible applications, especially in aquaculture industry, where pathogenic threat and antibacterial resistance are serious concerns. Bacillus stercoris MBTDCMFRI Ba37 isolated from mangrove environment of tropical estuarine habitats of Cochin exhibited a wide spectrum of antibacterial activity against major aquaculture pathogens belonging to genus Vibrio and Aeromonas. The structural characterization of the antibacterial compound from this strain may help in identifying their role as a biocontrol agent in aquaculture and allied sectors. The highest antibacterial activity was detected in 3rd day culture, grown in a modified Bacillus medium containing 1% of glycerol and 0.5% of glutamic acid at 30 °C, pH 8.0 and 15 ppt saline conditions. The inhibitory activity of the cell free supernatant was evident even at 20% v/v dilution. Preliminary studies on the nature of antibacterial action indicated that the bioactive principle is stable at temperatures up to 70 °C, between pH 6-9 and instable to lyzozyme and proteolytic enzymes. Bioassay guided purification followed by spectroscopic characterization of active fractions of B. stercoris MBTDCMFRI Ba37 revealed that the compound 1-(1-Hydroxyethyl)-1,7,10,12,13,15,17 heptamethyl-16-oxatetracyclo[8.7.0.02,3.012,13]heptadecan-5-one, is responsible for its major antibacterial activity. This is the first report on isolation and characterization of an antibacterial compound from the species B. stercoris. The results of this study indicated that B. stercoris MBTDCMFRI Ba37 has beneficial antibacterial properties which could be useful in developing novel antimicrobial therapeutics against a variety of aquaculture and other pathogens.
Asunto(s)
Antiinfecciosos/aislamiento & purificación , Bacillus/química , Cetonas/aislamiento & purificación , Vibrio/efectos de los fármacos , Antiinfecciosos/química , Antiinfecciosos/farmacología , Acuicultura , Medios de Cultivo/química , Medios de Cultivo/farmacología , Ecosistema , Cetonas/química , Cetonas/farmacología , Pruebas de Sensibilidad Microbiana , Probióticos/química , Probióticos/farmacología , Vibrio/patogenicidadRESUMEN
Six new polyketone metabolites, compounds (1-6) and seven known polyketone compounds (7-13) were isolated from Rhodiola tibetica endophytic fungus Alternaria sp. The structural elucidation of five new polyketone metabolites were elucidated on the basis of spectroscopic including 2D NMR and HRMS and spectrometric analysis. Inhibition rate evaluation revealed that compounds 1(EC50 = 0.02 mM), 3(EC50 = 0.3 mM), 6(EC50 = 0.07 mM), 8(EC50 = 0.1 mM) and 9(EC50 = 0.04 mM) had inhibitory effect on the SARS-CoV-2 virus.
Asunto(s)
Alternaria/química , Antivirales/aislamiento & purificación , Antivirales/farmacología , Cetonas/aislamiento & purificación , Cetonas/farmacología , Polímeros/aislamiento & purificación , Polímeros/farmacología , SARS-CoV-2/efectos de los fármacos , Antivirales/química , Humanos , Cetonas/química , Estructura Molecular , Polímeros/químicaRESUMEN
Rehmanniae Radix Praeparata is the processed products of the root of Rehmannia glutinosa. It has been used as a Traditional Chinese Medicine for thousands of years, and it has been found to possess widely pharmacological activities. In this study, three new 2,2'-difurylketone derivatives (rehmanniaeketone A-C) and two new chromones [3,8-dihydroxy-2-(2-hydroxyethyl)chromone and 3,8-dihydroxy-2-[(2-O-α-D-galactopyranosyloxy)ethyl]chromone] were isolated from the Rehmanniae Radix Praeparata. Furthermore all of the compounds were subjected to cytotoxic testing against the human lung carcinoma A549 cells. The cytotoxic results showed that rehmanniaeketone B and rehmanniaeketone C exhibited more stronger inhibition effects on the cell activity of A549 cells with the IC50 5.23â µM and 2.05â µM than other compounds. And 3,8-dihydroxy-2-(2-hydroxyethyl)chromone exhibited moderately inhibitory activity with the IC50 61â µM. Rehmanniaeketone A and 3,8-dihydroxy-2-[(2-O-α-D-galactopyranosyloxy]chromone showed no inhibitory effects.
Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Cromonas/farmacología , Medicamentos Herbarios Chinos/farmacología , Cetonas/farmacología , Rehmannia/química , Células A549 , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/aislamiento & purificación , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Cromonas/química , Cromonas/aislamiento & purificación , Relación Dosis-Respuesta a Droga , Ensayos de Selección de Medicamentos Antitumorales , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/aislamiento & purificación , Humanos , Cetonas/química , Cetonas/aislamiento & purificación , Medicina Tradicional China , Estructura Molecular , Células Tumorales CultivadasRESUMEN
The African weaver ant, Oecophylla longinoda, is used as a biological control agent for the management of pests. The ant has several exocrine glands in the abdomen, including Dufour's, poison, rectal, and sternal glands, which are associated with pheromone secretions for intra-specific communication. Previous studies have analyzed the gland secretions of Dufour's and poison glands. The chemistry of the rectal and sternal glands is unknown. We re-analyzed the secretions from Dufour's and poison glands plus the rectal and sternal glands to compare their chemistries and identify additional components. We used the solid-phase microextraction (SPME) technique to collect gland headspace volatiles and solvent extraction for the secretions. Coupled gas chromatography-mass spectrometry (GC-MS) analysis detected a total of 78 components, of which 62 were being reported for the first time. These additional components included 32 hydrocarbons, 12 carboxylic acids, 5 aldehydes, 3 alcohols, 2 ketones, 4 terpenes, 3 sterols, and 1 benzenoid. The chemistry of Dufour's and poison glands showed a strong overlap and was distinct from that of the rectal and sternal glands. The different gland mixtures may contribute to the different physiological and behavioral functions in this ant species.
Asunto(s)
Hormigas/química , Glándulas Exocrinas/química , Control Biológico de Vectores , Abdomen , Alcoholes/química , Alcoholes/aislamiento & purificación , Aldehídos/química , Aldehídos/aislamiento & purificación , Animales , Hormigas/metabolismo , Ácidos Carboxílicos/química , Ácidos Carboxílicos/aislamiento & purificación , Cromatografía de Gases y Espectrometría de Masas , Hidrocarburos/química , Hidrocarburos/aislamiento & purificación , Cetonas/química , Cetonas/aislamiento & purificación , Feromonas/biosíntesis , Feromonas/química , Feromonas/aislamiento & purificación , Microextracción en Fase Sólida , Esteroles/química , Esteroles/aislamiento & purificación , Terpenos/química , Terpenos/aislamiento & purificaciónRESUMEN
The present study was aimed at analyzing the chemical components of the essential oil from six Pyrrosia species by GC/MS and evaluating their inâ vitro antibacterial activities. Seventy volatile compounds were identified in the essential oil of six Pyrrosia samples. The identified volatile components were divided into following nine categories: aldehydes, terpenoids, fatty acids, ketones, furans, hydrocarbons, alcohols, esters, and phenols. The major components of the essential oil were 2,4-pentadienal, phytol and nonanal. The antimicrobial assays showed that the essential oils from Pyrrosia samples exhibited a broad-spectrum antimicrobial activity. However, P. lingua had the highest antibacterial activity against Staphylococcus aureus (ATCC 25923) with a minimum inhibitory concentration (MIC) of 2.5 µL/mL. This article is the first report of the chemical components and antimicrobial activity of the essential oil from six Pyrrosia species, which will lay the foundation for developing medicinal resources from Pyrrosia fronds.
Asunto(s)
Antibacterianos/farmacología , Aceites Volátiles/farmacología , Polypodiaceae/química , Staphylococcus aureus/efectos de los fármacos , Alcoholes/química , Alcoholes/aislamiento & purificación , Alcoholes/farmacología , Aldehídos/química , Aldehídos/aislamiento & purificación , Aldehídos/farmacología , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Ésteres/química , Ésteres/aislamiento & purificación , Ésteres/farmacología , Ácidos Grasos/química , Ácidos Grasos/aislamiento & purificación , Ácidos Grasos/farmacología , Furanos/química , Furanos/aislamiento & purificación , Furanos/farmacología , Hidrocarburos/química , Hidrocarburos/aislamiento & purificación , Hidrocarburos/farmacología , Cetonas/química , Cetonas/aislamiento & purificación , Cetonas/farmacología , Pruebas de Sensibilidad Microbiana , Aceites Volátiles/química , Aceites Volátiles/aislamiento & purificación , Fenoles/química , Fenoles/aislamiento & purificación , Fenoles/farmacología , Especificidad de la Especie , Terpenos/química , Terpenos/aislamiento & purificación , Terpenos/farmacologíaRESUMEN
The aim of this study was to evaluate the development of volatile compounds in yogurt samples obtained from goats fed a dietary supplementation with olive leaves (OL). For this purpose, thirty Saanen goats were divided into two homogeneous groups of 15 goats each: a control group that received a standard diet (CG) and an experimental group whose diet was supplemented with olive leaves (OLG). The trial lasted 28 days, at the end of which the milk of each group was collected and used for yogurt production. Immediately after production, and after 7 days of storage at 4 °C in the absence of light, the yogurt samples were characterized in terms of fatty acid profile, oxidative stability and volatile compounds by the solid-phase microextraction (SPME)-GC/MS technique. Dietary OL supplementation positively affected the fatty acid composition, inducing a significant increase in the relative proportion of unsaturated fatty acids, mainly oleic acid (C18:1 cis9) and linolenic acid (C18:3). With regard to the volatile profile, both in fresh and yogurt samples stored for 7 days, the OL supplementation induced an increase in free fatty acids, probably due to an increase in lipolysis carried out by microbial and endogenous milk enzymes. Specifically, the largest variations were found for C6, C7, C8 and C10 free fatty acids. In the same samples, a significant decrease in aldehydes, mainly heptanal and nonanal, was also detected, supporting-at least in part-an improvement in the oxidative stability. Moreover, alcohols, esters and ketones appeared lower in OLG samples, while no significant variations were observed for lactones. These findings suggest the positive role of dietary OL supplementation in the production of goats' milk yogurt, with characteristics potentially indicative of an improvement in nutritional properties and flavor.
Asunto(s)
Alimentación Animal , Ácidos Grasos no Esterificados/aislamiento & purificación , Ácidos Grasos Insaturados/aislamiento & purificación , Olea/química , Compuestos Orgánicos Volátiles/aislamiento & purificación , Yogur/análisis , Alcoholes/clasificación , Alcoholes/aislamiento & purificación , Aldehídos/aislamiento & purificación , Animales , Ésteres/clasificación , Ésteres/aislamiento & purificación , Ácidos Grasos no Esterificados/clasificación , Ácidos Grasos Insaturados/clasificación , Femenino , Cromatografía de Gases y Espectrometría de Masas , Cabras , Cetonas/clasificación , Cetonas/aislamiento & purificación , Lactonas/clasificación , Lactonas/aislamiento & purificación , Leche/química , Hojas de la Planta/química , Microextracción en Fase Sólida/métodos , Compuestos Orgánicos Volátiles/clasificaciónRESUMEN
Using antibiotics as feed additives have been successively banned worldwide from 1986; therefore, it is an urgent task to finding safe and effective alternatives. As natural products of plant origin, essential oils (EOs) are an outstanding option due to their reported bioactivity. In this research, ten EOs of Labiatae species were extracted by steam distillation and its chemical constituents were identified by gas chromatography-mass spectrometry (GC-MS). A total of 123 chemical compounds, including alkenes, phenols, aldehydes and ketones, were identified. The results of antioxidant activity carried out through DPPH free radical scavenging (DPPH) and ferric reducing antioxidant power (FRAP), showing that EOs of Ocimum basilicum Linn. (ObEO), Thymus mongolicus Ronn. (TmEO), Origanum vulgare Linn. (OvEO) and Mosla chinensis Maxim. (McEO) have strong antioxidant activities. Their 50%-inhibitory concentration (IC50) value was <1.00, 1.42, 1.47 and 1.92 µg/mL, respectively; and their FRAP value was 1536.67 ± 24.22, 271.84 ± 4.93, 633.71 ± 13.14 and 480.66 ± 29.90, respectively. The results of filter paper diffusion showing that McEO, OvEO and TmEO inhibition zone diameter (IZD) are all over 30 mm. The results of two-fold dilution method showed that McEO, OvEO and TmEO have strong antibacterial activities against Staphylococcus aureus (S. aureus) and their minimal inhibitory concentrations (MIC) value was 1 µL/mL, 2 µL/mL, and 2 µL/mL, respectively. In conclusion, the results in this work demonstrate the possibility for development and application of EOs as potential feed additives.
Asunto(s)
Antibacterianos/farmacología , Antioxidantes/farmacología , Compuestos de Bifenilo/antagonistas & inhibidores , Lamiaceae/química , Aceites Volátiles/química , Picratos/antagonistas & inhibidores , Staphylococcus aureus/efectos de los fármacos , Aldehídos/química , Aldehídos/aislamiento & purificación , Aldehídos/farmacología , Alquenos/química , Alquenos/aislamiento & purificación , Alquenos/farmacología , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antioxidantes/química , Antioxidantes/aislamiento & purificación , Cetonas/química , Cetonas/aislamiento & purificación , Cetonas/farmacología , Pruebas de Sensibilidad Microbiana , Fenoles/química , Fenoles/aislamiento & purificación , Fenoles/farmacologíaRESUMEN
BACKGROUND: Water absorption is the dominant factor affecting the quality deterioration of dried Lentinus edodes. We therefore analyzed the effect of moisture content and dynamic water status on physical properties of the mushroom stored at water activity (aw ), 0.33, 0.43, 0.67, 0.76, and 0.84 for 50 days. Moisture mobility and water status were analyzed using low-field nuclear magnetic resonance, while hardness and microstructure were determined as texture characteristics. Meanwhile, an electronic nose and headspace solid-phase micro-extraction combined with gas chromatography-mass spectrometry (HS-SPME-GC-MS) were used to analyze the flavor properties of dried L. edodes. RESULTS: The results showed that bound water was the dominant water status in dried L. edodes. The content and molecular mobility of bound water increased at aw = 0.67, 0.76, and 0.84. This contributed to discoloration, hardness loss, and microstructure sparsity of dried L. edodes. The increasing content and molecular mobility of bound water aggravated the deterioration of characteristic flavor by reducing acid, aldehyde, and ketone content. CONCLUSION: Unlike immobilized or free water, bound water had a critical influence on the quality deterioration of dried L. edodes during storage. © 2019 Society of Chemical Industry.
Asunto(s)
Hongos Shiitake/química , Agua/química , Aldehídos/química , Aldehídos/aislamiento & purificación , Nariz Electrónica , Aromatizantes/química , Aromatizantes/aislamiento & purificación , Almacenamiento de Alimentos , Cromatografía de Gases y Espectrometría de Masas , Cetonas/química , Cetonas/aislamiento & purificación , Microextracción en Fase SólidaRESUMEN
In this study, a series of novel CD chiral stationary phases were fabricated by immobilization of mono-6A -deoxy-N3 -cyclodextrin onto silica surfaces followed by click regulation of CD primary face with 4-pentynoic acid (acidic moiety), 2-propynylamine (alkaline moiety) and L-propargylglycine (chiral amino acid moiety), respectively. Enantioseparations of various kinds of racemates including dansyl-amino acids, chiral lactides and diketones were conducted in reversed phase modes on these chiral stationary phases, where nearly forty diketones and chiral lactides were firstly separated on cyclodextrin stationary phases. 4-Pentynoic acid moiety can make the retention ability decline while amine moiety significantly enhanced the retention ability of the stationary phases. For most of the studied analytes, the chiral amino acid moiety had the most positive effects on both the retention time and the resolution. The inclusion complexation between chiral analytes and cyclodextrins were also investigated by fluorescence method.
Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Ciclodextrinas/química , Aminoácidos/análisis , Aminoácidos/química , Aminoácidos/aislamiento & purificación , Química Clic , Cetonas/análisis , Cetonas/química , Cetonas/aislamiento & purificación , Reproducibilidad de los Resultados , EstereoisomerismoRESUMEN
A reliable Headspace-Solid Phase Microextraction (HS-SPME) method was developed for the determination of polar volatile components of commercial nut-based milk alternative drinks prior to Gas Chromatography-Mass Spectrometry (GC-MS) analysis. Under the optimum extraction conditions, a divinylbenzene (DVB)/Carboxen™ CAR)/polydimethylsiloxane (PDMS) fiber was used and 2 mL of sample was heated at 60 °C for 40 min under stirring, without salt addition. Ten compounds from different chemical classes (heptane, a-pinene, toluene, 2-methylpyrazine, 3-heptanone, heptanal, 2-octanone, 1-heptanol, benzaldehyde and 1-octanol) were chosen as model analytes for quantification. Limits of detection and limits of quantification were found to be 0.33-1.67 ng g-1 and 1-5 ng g-1, accordingly. Good linearity, precision and accuracy were obtained as well as a wide linear range. The proposed method was successfully applied to various beverages including almond milk, walnut milk, peanut milk and almond chocolate milk. More than 70 volatile compounds were detected in the different samples. Most of the detected volatiles were aldehydes, ketones and alcohols. This technique can be used for the determination of volatile compounds in nut-based beverages, to detect compositional changes during storage and technological treatment used for their production.
Asunto(s)
Bebidas/análisis , Nueces/química , Compuestos Orgánicos Volátiles/análisis , Alcoholes/aislamiento & purificación , Aldehídos/aislamiento & purificación , Cromatografía de Gases y Espectrometría de Masas , Cetonas/aislamiento & purificación , Límite de Detección , Microextracción en Fase Sólida , Compuestos Orgánicos Volátiles/aislamiento & purificaciónRESUMEN
The methanol extract of the flowers of the Australian eucalypt tree Corymbia torelliana yielded six new ß-triketone-flavanone hybrids, torellianones A-F (1-6), the tetrahydroxycyclohexane torellianol A (7), and known ß-triketones (4 S)-ficifolidione (8) and (4 R)-ficifolidione (9), and ß-triketone-flavanones kunzeanone A (10) and kunzeanone B (11). Torellianones A and B, C and D, and E and F were each isolated as inseparable diastereomeric mixtures. Exchange correlations observed in a ROESY spectrum indicated that 5 and 6 also interconverted between stable conformers. The structures of 1-7 were elucidated from the analysis of 1D/2D NMR and MS data. Relative configurations of torellianones C-F and torrellianol A were determined from analysis of ROESY data. Compounds 1-10 were tested for antiplasmodial activity against a drug-sensitive (3D7) strain of Plasmodium falciparum, with 3-6 and 8-10 showing limited antiplasmodial activity, with IC50 values ranging from 3.2 to 16.6 µM.
Asunto(s)
Antimaláricos/aislamiento & purificación , Flavanonas/aislamiento & purificación , Cetonas/aislamiento & purificación , Myrtaceae/química , Extractos Vegetales/farmacología , Antimaláricos/farmacología , Flavanonas/química , Flavanonas/farmacología , Flores/química , Células HEK293 , Humanos , Cetonas/química , Cetonas/farmacología , Espectroscopía de Resonancia Magnética , Estructura Molecular , Extractos Vegetales/química , Árboles/químicaRESUMEN
Bradysia procera is a serious insect pest of Panax ginseng plants. This study was conducted to determine the toxicity and mechanism of action of three phenylpropanoids, three terpenoids, and a ketone from Syzygium aromaticum bud methanol extract and hydrodistillate against third-instar larvae and eggs of B. procera. In a filter-paper mortality bioassay, methyl salicylate (LC50, 5.26µg/cm2) was the most toxic compound, followed by 2-nonanone, eugenol, and eugenyl acetate (8.77-15.40µg/cm2). These compounds were significantly less toxic than either thiamethoxam, clothianidin, or cypermethrin. Egg hatching was inhibited by 97, 85, and 40% at 11.7µg/cm2 of methyl salicylate, 2-nonanone, and eugenol, respectively. The egg-hatching inhibition of these insecticides was between 90 and 94% at 0.09µg/cm2. These constituents were consistently more toxic in closed versus open containers, indicating that toxicity was achieved mainly through the action of vapor. The mechanism of larvicidal action of methyl salicylate, eugenol, and eugenyl acetate might be primarily due to interference with the octopaminergic system. 2-Heptyl acetate and 2-nonanone might act on both acetylcholinesterase and the octopaminergic receptor. 2-Heptanone might act primarily on acetylcholinesterase. Further studies will warrant possible applications of S. aromaticum bud-derived products as potential larvicides and ovicides for the control of B. procera.
Asunto(s)
Dípteros/efectos de los fármacos , Insecticidas/farmacología , Cetonas/aislamiento & purificación , Larva/efectos de los fármacos , Óvulo/efectos de los fármacos , Fenilpropionatos/aislamiento & purificación , Extractos Vegetales/farmacología , Syzygium/metabolismo , Acetilcolinesterasa/efectos de los fármacos , Animales , Dípteros/crecimiento & desarrollo , Cromatografía de Gases y Espectrometría de Masas , Cetonas/farmacología , Aceites Volátiles/farmacología , Fenilpropionatos/farmacología , Receptores de Amina Biogénica/efectos de los fármacos , Terpenos/aislamiento & purificación , Terpenos/farmacologíaRESUMEN
Callistrilones F - K (1 - 6), six new triketone-phloroglucinol-monoterpene hybrids were isolated from the twigs and leaves of Callistemon rigidus. Their structures with absolute configurations were established by a combination analysis of NMR spectra, X-ray diffraction, and electronic circular dichroism (ECD) calculations. Compounds 3 and 4 exhibited moderate inhibitory activities against herpes simplex virus (HSV-1) with IC50 values of 10.00 ± 2.50 and 12.50 ± 1.30 µm, respectively.
Asunto(s)
Antivirales/farmacología , Cetonas/farmacología , Monoterpenos/farmacología , Myrtaceae/química , Floroglucinol/farmacología , Simplexvirus/efectos de los fármacos , Antivirales/química , Antivirales/aislamiento & purificación , Relación Dosis-Respuesta a Droga , Cetonas/química , Cetonas/aislamiento & purificación , Pruebas de Sensibilidad Microbiana , Conformación Molecular , Monoterpenos/química , Monoterpenos/aislamiento & purificación , Floroglucinol/química , Floroglucinol/aislamiento & purificación , Estereoisomerismo , Relación Estructura-ActividadRESUMEN
Milled Roselle (Hibiscus sabdariffa L.) seeds of the UMKL cultivar were analyzed for proximate composition, water and oil absorption capacity, and the influence of storage conditions on storage stability. The storage stability was determined under four types of conditions: light/oxygen (air) (LO), light/nitrogen (LN), darkness/oxygen (air) (DO), and darkness/nitrogen (DN) while monitoring for seven consecutive months. During the storage period, the formation of volatiles was determined using dynamic headspace sampling and Gas Chromatography-Mass Spectrometry (GC-MS) analysis. In total, 85 volatiles were identified, mainly aldehydes, alcohols, ketones, furans, and acids indicating lipid oxidation. It is recommended that milled Roselle seeds should be flushed with nitrogen and stored in darkness. Under these conditions, the seeds can be stored for at least three months without changes in volatile profile. This is important to ensure the good quality of milled Roselle seeds for further commercialization.
Asunto(s)
Almacenamiento de Alimentos/métodos , Hibiscus/química , Semillas/química , Compuestos Orgánicos Volátiles/química , Alcoholes/química , Alcoholes/aislamiento & purificación , Alcoholes/metabolismo , Aldehídos/química , Aldehídos/aislamiento & purificación , Aldehídos/metabolismo , Furanos/química , Furanos/aislamiento & purificación , Furanos/metabolismo , Cromatografía de Gases y Espectrometría de Masas , Hibiscus/efectos de los fármacos , Hibiscus/metabolismo , Cetonas/química , Cetonas/aislamiento & purificación , Cetonas/metabolismo , Luz , Nitrógeno/farmacología , Oxidación-Reducción , Oxígeno/farmacología , Semillas/efectos de los fármacos , Semillas/metabolismo , Compuestos Orgánicos Volátiles/aislamiento & purificación , Compuestos Orgánicos Volátiles/metabolismoRESUMEN
Natural amino acids are well known to form coordination polymers with transition metal ions. In this study, six homochiral metal-organic frameworks constructed from Zn2+ or Co2+ ions and various enantiopure amino acid (L-tyrosine, L-histidine, L-tryptophan and L-glutamic acid), namely [Zn(L-tyr)]n (L-tyrZn), [Zn4 (btc)2 (Hbtc)(L-His)2 (H2 O)4 ]·1.5H2 O, {[Zn2 (L-trp)2 (bpe)2 (H2 O)2 ]·2H2 O·2NO3 }n , [Co2 (L-Trp)(INT)2 (H2 O)2 (ClO4 )], [Co2 (sdba)((L-Trp)2 ] and [Co(L-Glu)(H2 O)·H2 O]∞ , were synthesized according to the methods previously reported in the literature. The six homochiral MOFs were explored as the chiral stationary phases for high-performance liquid chromatographic separation of enantiomers using hexane/isopropanol or hexane/dichloromethane as mobile phase. Various types of enantiomers such as alcohols, amines, ketones, ethers, organic acids, etc. can be resolved on these homochiral MOF columns. The results revealed that the enantioseletivities of homochiral MOFs based on amino acids as chiral bridging ligands used as stationary phases are practical in HPLC.
Asunto(s)
Aminoácidos/química , Cromatografía Líquida de Alta Presión/métodos , Estructuras Metalorgánicas/química , Polímeros/química , 2-Propanol/química , Alcoholes/aislamiento & purificación , Aminas/aislamiento & purificación , Cromatografía Líquida de Alta Presión/instrumentación , Éteres/aislamiento & purificación , Hexanos/química , Cetonas/aislamiento & purificación , Cloruro de Metileno/química , EstereoisomerismoRESUMEN
Chemical investigations of the MeOH extract of air dried flowers of the Australian tree Angophora woodsiana (Myrtaceae) yielded two new ß-triketones, woodsianones A and B (1, 2) and nine known ß-triketones (3-11). Woodsianone A is a ß-triketone-sesquiterpene adduct and woodsianone B is a ß-triketone epoxide derivative. The structures of the new and known compounds were elucidated from the analysis of 1D/2D NMR and MS data. The relative configurations of the compounds were determined from analysis of 1H-1H coupling constants and ROESY correlations. All compounds (1-11) had antiplasmodial activity against the chloroquine sensitive strain 3D7. The known compound rhodomyrtone (5) and new compound woodsianone B (2) showed moderate antiplasmodial activities against the 3D7 strain (1.84µM and 3.00µM, respectively) and chloroquine resistant strain Dd2 (4.00µM and 2.53µM, respectively).
Asunto(s)
Antimaláricos/química , Cetonas/química , Myrtaceae/química , Extractos Vegetales/química , Antimaláricos/aislamiento & purificación , Antimaláricos/farmacología , Australia , Supervivencia Celular/efectos de los fármacos , Cloroquina/farmacología , Resistencia a Medicamentos/efectos de los fármacos , Flores/química , Flores/metabolismo , Células HEK293 , Humanos , Cetonas/aislamiento & purificación , Cetonas/farmacología , Espectroscopía de Resonancia Magnética , Conformación Molecular , Myrtaceae/metabolismo , Plasmodium falciparum/efectos de los fármacos , Sesquiterpenos/químicaRESUMEN
Three new isoaigialones, A, B, and C (1-3), along with aigialone (4), were isolated from the crude EtOAc extract of a Phaeoacremonium sp., an endophytic fungus obtained from the leaves of Senna spectabilis. The structures of these compounds were elucidated based on the analysis of spectroscopic data. Compounds 2 and 4 were active against the phytopathogenic fungi Cladosporium cladosporioides and C. sphaerospermum. This is the first report of metabolites produced by an Phaeoacremonium sp., associated with S. spectabilis.
Asunto(s)
Acetales/aislamiento & purificación , Acetales/farmacología , Antifúngicos/aislamiento & purificación , Antifúngicos/farmacología , Ascomicetos/química , Cladosporium/química , Cetonas/aislamiento & purificación , Cetonas/farmacología , Lactonas/aislamiento & purificación , Hojas de la Planta/química , Senna/química , Acetales/química , Antifúngicos/química , Cetonas/química , Lactonas/química , Lactonas/metabolismo , Lactonas/farmacología , Estructura MolecularRESUMEN
Two pairs of rare naturally occurring racemic lipids, (±)-4,7-dihydroxy-4-methyl-2,5-heptanedione (1), and (±)-7-butoxy-4-hydroxy-4-methyl-2,5-heptanedione (2) were isolated from the red alga Chondria crassicaulis Harv. The structures of the racemic mixtures of 1 and 2 were elucidated by detailed spectroscopic techniques, including 1D and 2D NMR (1H and 13C NMR, 1H-1H COSY, HSQC, and HMBC) as well as mass spectrometry and optical rotation experiments, and by comparison with data for related known analogs. This is the first report of naturally occurring 4-hydroxy-4-methyl-2,5-heptanedione derivatives. Antifungal, PTP1B inhibitory, and receptor tyrosine kinase inhibitory activities of these two compounds were investigated. The results showed that compounds 1 and 2 exhibited good selective inhibition against RET tyrosine kinase activity with IC50 values of 9.56 and 8.93 µM, respectively. Compound 1 also displayed moderate antifungal activity against Cryptococcus neoformans (32609), showing a MIC80 value of 32 µg/ml.