Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/16071
Título: Triterpenes and the antimycobacterial activity of duroia macrophylla huber (Rubiaceae)
Autor: Martins, Daiane
Carrion, Lillian Lucas
Ramos, Daniela Fernandes
Salomé, Kahlil Schwanka
Silva, Pedro A. da
Barison, Andersson
Nunez, C. V.
Palavras-chave: Duroia Macrophylla Extract
Flavonoid
Oleanolic Acid
Plant Extract
Unclassified Drug
Ursolic Acid
Antiinfective Agent
Phenol Derivative
Plant Extract
Tannin Derivative
Triterpene
Antibacterial Activity
Carbon Nuclear Magnetic Resonance
Drug Isolation
Duroia Macrophylla
Heteronuclear Multiple Bond Correlation
Minimum Inhibitory Concentration
Mycobacterium Tuberculosis
Nonhuman
Phytochemistry
Plant Leaf
Proton Nuclear Magnetic Resonance
Rubiaceae
Chemistry
Drug Effect
Hydrolysis
Metabolism
Microbial Sensitivity Test
Mycobacterium Tuberculosis
Nuclear Magnetic Resonance Spectroscopy
Reproducibility
Anti-bacterial Agents
Hydrolysis
Magnetic Resonance Spectroscopy
Microbial Sensitivity Tests
Mycobacterium Tuberculosis
Phenols
Plant Extracts
Plant Leaves
Reproducibility Of Results
Rubiaceae
Tannins
Triterpenes
Data do documento: 2013
Revista: BioMed Research International
É parte de: Volume 2013
Abstract: Duroia macrophylla popularly known as "cabeça-de-urubú, " "apuruí," or "puruí-grande-da-mata" occurs in the Amazon Forest. Its leaves and branches were collected twice and extracted with dichloromethane and methanol. All extracts were subjected to phytochemical investigation and terpenes and flavonoids were found in all dichloromethane and methanol extracts, respectively. Methanol extracts from both branches (1st collection) and leaves (2nd collection) presented hydrolyzed tannins, yet alkaloids were only detected in the dichloromethane and methanol extracts from branches at the 2nd collection. Phenol compounds were found in both dichloromethane extracts' collections. The action of every extract was assayed against Mycobacterium tuberculosis (RMPr, H37Rv, and INHr strains), showing that the dichloromethane extract from leaves (1st collection) has the major biological activity, with a MIC of 6.25 μg/mL for the INHr strain, 25.0 μg/mL for the RMPr strain, and ≤6.25 μg/mL for the H37Rv strain. The chromatographic fractioning of the dichloromethane extract from leaves (1st collection) yielded the isolation of two triterpenes: oleanolic and ursolic acids, which were identified by NMR analysis and reported for the first time in the Duroia genus. © 2013 Daiane Martins et al.
DOI: 10.1155/2013/605831
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