Estudo químico e biológico das folhas de Piranhea trifoliata Baill e de seus fungos endofíticos

Abstract

This work aimed to study the chemical extracts of Piranhea trifoliata and your endophytes (PICRODENDRACEAE) and its potential antimicrobial tests, antioxidant and antimalarial. The leves it was collected in Volta Grande of Xingú, Altamira, PA (collect 1) and Lake of Catalão, Manaus, AM (collect 2 e 3). The dried specimen’s it was deposited in the herbarium of the Federal Institute of Amazonas (IFAM) with record numbers 10653 and 10654. The collected material was dried and pulverized. The collect 1, was extracted by dichloromethane (DCM), methanol (MeOH) and water (H2O). The collect 2 and 3 was extracted by hexane, methanol and water. The preliminary phytochemical analysis of leaves and fungi showed that dichlorometane and hexane extracts contain terpenes and methanolic extracts contain phenolic compounds. The broths from fungi showed that diclorometânica phase (DCM) contain terpenes, and phase of Ethyl Acetate (AcOEt) contain terpene and phenolic compounds. The phytochemical study of the leves led to the isolation of: Friedelan-3-one (I), 30-hydroxy-friedelan-3-one (II), Lupeol (III), the mixture of β -Sitosterol and Stigmasterol steroids (IV and V), hydroxycoriatin (VI), the mixture of α and β-amyrin (VII and VIII ), 7- hydroxy-6-methoxy-coumarin (IX), 7,4 ''' dymethylamentoflavone (X), methyllonyflavna 3'-O-(XI) and purification of the 28-hydroxy-friedelan-3-one (XIV). The phytochemical study of the Diaporthe hongkongensis, fungi, led to the isolation of (3-oxociclobutil) 2-methyl-1- hydroxi metilciclopenta -2,4- diene carboxylate (XII) and 9-amino-7- (2,5,7-triazabicyclo [2.2.1] hept-3-yl)-2,3,6- trioxi-1-azabicyclo [3.2.2] nona-4,8-diene-4- carbaldehyde (XIII) both isollated of the first time. All compound were identified by 1H, 13C NMR, 2D and mass espectra data. The antioxidant activity, shoed the MeOH extract of leaves from collection 2, was equivalent with 1,15 and 1,13, the H2O phase showed 2,8 and 4.,51 (DPPH• and Fe3+) were considered significant. The antibacterial activity the DCM phase of leaves of collectes 2 and 3 and the EtOAc phase of collection 1, showed CIM and CMB found was 500/mL against Aeromonas hydrophila and Flavobacterium columnare. The aqueous phase of collection 1 showed CIM and CMB found was 1000 μg/ml against Flavobacterium columnare and Pseudomonas fluorescens. The mycelial extracts of fungi 4 and 6, tested with methodology to inhibition halo, showed medium activity, 1 cm, against Aeromonas hydrophila and Klebsiella pneumoniae. The DCM and EtOAc phases of metabolite broth of the fungu 4, showed activity with halo of 1 and 1,2 cm. The antimalical activity. The antimalarial activity showed that hexane and MeOH extracts of leves of the collection 3, showed IC50 of 1,51 and 1,77 mg/mL when compared to the standard. The MeOH extract of fungi 4, showed 6,89 of parasitaemia being significant. The activity by isolated compound sowed CIM of 73,58% to the compound X and 71,75% to the compound XI against Klebsiella pneumoniae .