RESUMEN
Two undescribed frenolicins H and I (1 and 2) along with six previously described frenolicin analogues [frenolicins A (3), B (4), UCF76-B (5), E - G (6 - 8)] and two anthraquinones [3,8-dihydroxy-1-propylanthraquinone-2-carboxylic acid (9) and 3,8-dihydroxy-1-propylanthraquinone (10)] were isolated from a longkong bark eating caterpillar-derived Streptomyces sp. TBRC17107. The chemical structures were determined by NMR spectroscopic information and HRESIMS data. Frenolicins H (1) and I (2) showed weak cytotoxicity against malignant and non-malignant cells. Frenolicins A (3) and B (4) showed antimalarial activity against Plasmodium falciparum (IC50 17.4 and 1.37 µM), antibacterial activity against Bacillus cereus and Staphylococcus aureus (MIC 50.0 and 0.20 µg/mL). Only frenolicin B had anti-plant pathogenic fungal activity against Collectotrichum acutatum and Alternaria brassicicola with MIC values of MIC 1.56 and 6.25 µg/mL, respectively. Frenolicins A and G possessed anti-Mycobacterium tuberculosis with equal MICs of 25.0 µg/mL.
RESUMEN
Fourteen new cytochalasans, brunnesins A-N (1-14), along with eleven known compounds, were isolated from the culture extracts of the insect pathogenic fungus Metarhizium brunneum strain TBRC-BCC 79240. The compound structures were established by spectroscopy, X-ray diffraction analysis, and electronic circular dichroism. Compound 4 exhibited antiproliferative activity against all cell lines tested (mammalian), with 50% inhibition concentration (IC50) values ranging from 2.09 to 16.8 µg mL-1. Compounds 6 and 16 were shown to be bioactive only against non-cancerous Vero cells (IC50 4.03 and 0.637 µg mL-1, respectively) whereas compounds 9 and 12 were bioactive only against NCI-H187 small-cell lung cancer cells (IC50 18.59 and 18.54 µg mL-1, respectively). Compounds 7, 13, and 14 showed cytotoxicity against NCI-H187 and Vero cell lines with IC50 values ranging from 3.98-44.81 µg mL-1.
RESUMEN
Three undescribed abyssomicin derivatives, including microbimisin, abyssomicins Z1, and Z2, were isolated from the soil actinomycete Microbispora rhizosphaerae sp. nov. TBRC6028. Chemical structures were determined by NMR spectroscopic data (1H, 13C, COSY, HSQC, HMBC, and NOESY spectra) and the absolute configurations were verified by single-crystal X-ray diffraction analyses together with the ECD spectral data. Microbimisin and abyssomicin Z1 exhibited weak antibacterial activity against Bacillus cereus with MIC values of 25.0 and 50.0 µg/mL without cytotoxicity against MCF-7 and Vero cells at the concentration of 50 µg/mL.
Asunto(s)
Actinobacteria , Rizosfera , Animales , Chlorocebus aethiops , ADN Bacteriano , Filogenia , ARN Ribosómico 16S , Suelo , Células VeroRESUMEN
Five new compounds, iranginins A-E (1-5), together with sixteen known compounds were isolated from the insect pathogenic fungus Ophiocordyceps irangiensis BCC 2728. The structures and the absolute configurations of the new compounds were established by spectroscopic analyses, the application of modified Mosher's method (for 2), ECD calculation (for 5), and X-ray crystallographic analysis (for 4). LL-Z1640-5 and mucorisocoumarin C were active against Mycobacterium tuberculosis (MIC 41.7 and 85.0 µM, respectively), while peyroisocoumarin D exhibited cytotoxic activity (IC50 65.6 µM).
Asunto(s)
Antineoplásicos , Hormigas , Hypocreales , Policétidos , Animales , Estructura MolecularRESUMEN
Eight previously undescribed naturally-occurring compounds, including abyssomycins Y - Z, methyl aeruginoate, desferri-ferrithocin-4-hydroxyphenethylester, streptomethiocins A - B, furaquinocin I, and streptolactone, along with eleven known compounds were isolated from the endophytic Streptomyces sp. TBRC7642. The chemical structures were determined based on spectroscopic means including 1D, 2D NMR spectroscopy and mass spectrometry. The absolute configurations were assigned by relying on CD spectra and their optical rotations. In addition, the isolated compounds were evaluated for biological activity, such as antimalarial, antitubercular, antibacterial (both Gram-positive and Gram-negative bacteria), as well as for cytotoxicity against MCF-7, NCI-H187, and Vero cells.
Asunto(s)
Antimaláricos , Streptomyces , Animales , Antibacterianos , Chlorocebus aethiops , Bacterias Gramnegativas , Bacterias Grampositivas , Células VeroRESUMEN
Severe chili anthracnose disease in Thailand is caused by Colletotrichum gloeosporioides and C. capsici. To discover anti-anthracnose substances we developed an efficient dual-fluorescent labeling bioassay based on a microdilution approach. Indicator strains used in the assay were constructed by integrating synthetic green fluorescent protein (sGFP) and Discosoma sp. red fluorescent protein (DsRedExp) genes into the genomes of C. gloeosporioides or C. capsici respectively. Survival of co-spore cultures in the presence of inhibitors was determined by the expression levels of these fluorescent proteins. This developed assay has high potential for utilization in the investigation of selective inhibition activity to either one of the pathogens as well as the broad-range inhibitory effect against both pathogens. The value of using the dual-fluorescent assay is rapid, reliable, and consistent identification of anti-anthracnose agents. Most of all, the assay enables the identification of specific inhibitors under the co-cultivation condition.
Asunto(s)
Bioensayo , Capsicum/microbiología , Colletotrichum/aislamiento & purificación , Enfermedades de las Plantas/prevención & control , Esporas Fúngicas/aislamiento & purificación , Antifúngicos/química , Antifúngicos/farmacología , Colletotrichum/clasificación , Colletotrichum/genética , Colletotrichum/patogenicidad , Genes Reporteros , Ingeniería Genética , Proteínas Fluorescentes Verdes , Proteínas Luminiscentes , Microscopía Fluorescente , Enfermedades de las Plantas/microbiología , Esporas Fúngicas/clasificación , Esporas Fúngicas/genética , Esporas Fúngicas/patogenicidad , Tailandia , Proteína Fluorescente RojaRESUMEN
A novel 20-norpimarane glucoside, xylopimarane (1), together with the known sphaeropsidin C (2) and clonostachydiol (3), was isolated from the fungus Xylaria sp. BCC 4297. Compound 1 exhibited cytotoxicity to cancer cell lines KB, MCF-7, and NCI-H187 with respective IC(50) values of 1.0, 13, and 65 µM.
Asunto(s)
Antineoplásicos/aislamiento & purificación , Diterpenos/aislamiento & purificación , Glucósidos/aislamiento & purificación , Xylariales/química , Animales , Antineoplásicos/química , Antineoplásicos/farmacología , Chlorocebus aethiops , Diterpenos/química , Diterpenos/farmacología , Ensayos de Selección de Medicamentos Antitumorales , Femenino , Glucósidos/química , Glucósidos/farmacología , Glicósidos , Humanos , Concentración 50 Inhibidora , Células KB , Estructura Molecular , Tailandia , Células VeroRESUMEN
Cordyformamide (4), the plausible biogenetic precursor of xanthocillin Y2, was isolated from a culture broth of the insect pathogenic fungus Cordyceps brunnearubra BCC 1395. Cordyformamide was found to exhibit activity against the malarial parasite Plasmodium falciparum K1 with an IC50 value of 18 microM, whereas it showed weak or no cytotoxicity.
Asunto(s)
Alcaloides/aislamiento & purificación , Antimaláricos/aislamiento & purificación , Butadienos/química , Butadienos/aislamiento & purificación , Cordyceps/química , Insectos/microbiología , Fenoles/química , Fenoles/aislamiento & purificación , Plasmodium falciparum/efectos de los fármacos , Alcaloides/química , Alcaloides/farmacología , Animales , Antimaláricos/química , Antimaláricos/farmacología , Butadienos/farmacología , Humanos , Concentración 50 Inhibidora , Células KB , Estructura Molecular , Fenoles/farmacologíaRESUMEN
A new linear polyester, menisporopsin B, along with the known macrocyclic polyester, menisporopsin A, was isolated from the seed fungus Menisporopsis theobromae BCC 4162. The structure of menisposopsin B was addressed primarily by spectroscopic analyses, and the stereochemistry was established by chemical correlation. Menisporopsin B exhibited antimalarial activity with an IC(50) value of 1.0 microg/ml.