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1.
J Nat Prod ; 86(10): 2294-2303, 2023 10 27.
Artigo em Inglês | MEDLINE | ID: mdl-37675572

RESUMO

This article describes the structure revision of nine triterpenoids that have been reported corresponding to the same 13C NMR data set. In addition, 13C NMR calculation shows that some chemical shift assignments must be swapped. Our analysis improves the fit between the experimental and calculated data. Correcting misassigned structures and correctly assigning each signal is essential for elucidating new structurally related compounds. Furthermore, the ambiguity of several compounds, the structure of which differs in the literature and the Sci-Finder database, has been eliminated. Misassigned structures were found by chemical shift searches in NAPROC-13, and the results provide two or more different compounds with the same 13C NMR data. The process to determine the correct, most likely structural proposal in agreement with the experimental 13C NMR data was carried out by DFT calculations.


Assuntos
Produtos Biológicos , Produtos Biológicos/química , Espectroscopia de Ressonância Magnética/métodos , Imageamento por Ressonância Magnética , Teoria da Densidade Funcional , Estrutura Molecular
2.
J Nat Prod ; 86(4): 897-908, 2023 04 28.
Artigo em Inglês | MEDLINE | ID: mdl-36881492

RESUMO

A considerable number of natural products have been published in recent years with misassigned structure, even though they had been correctly elucidated in the past. The availability of databases containing revised structures can prevent the amplification of errors in structural elucidation. NAPROC-13, a dereplication tool based on the 13C chemical shift, has been used to search for substances that, possessing the same chemical shifts, have been described with different structures. The correct structure of these different structural proposals is verified by computational chemistry. This paper reports the structural revision of nine triterpenoids following this methodology.


Assuntos
Produtos Biológicos , Produtos Biológicos/química , Bases de Dados Factuais , Estrutura Molecular
3.
Rev. cuba. plantas med ; 25(1): 1-11, 2020. tab, graf
Artigo em Espanhol | MOSAICO - Saúde integrativa | ID: biblio-1223995

RESUMO

Introducción: Chrysobalanus icaco L. (Chrysobalanaceae) es un arbusto utilizado en la fitoterapia tradicional latinoamericana, pero en la provincia de Chiriquí se ha registrado el uso de su fruto para hacer conservas, no de forma medicinal. Objetivo: Caracterizar los metabolitos secundarios presentes en las hojas y semillas de Chrysobalanus icaco y evaluar su actividad biológica in vitro. Métodos: Los metabolitos secundarios presentes en los extractos de las hojas, semilla inmadura y madura de Chrysobalanus icaco, se detectaron a través de tamizaje fitoquímico y purificación por técnicas cromatográficas. Posteriormente se evaluó el contenido de polifenoles totales y la actividad antioxidante total de la infusión de las hojas, semillas y pulpa de esta especie, así como la actividad antibacteriana in vitro. Resultados: En las hojas se identificaron por tamizaje fitoquímico, flavonoides, glucósidos cardiotónicos, triterpenos y esteroides. Para la semilla inmadura se encontró presencia mayoritaria de mezclas de azucares, mientras que para la semilla madura se detectaron ácidos grasos en el endocarpio (almendra). Los datos de polifenoles totales en extractos de Icaco mostraron alto contenido de estos metabolitos en la infusión de hojas secas, y la inhibición del radical DPPH fue mayor también para las hojas secas de icaco, seguido de la infusión de semilla inmadura. Por otro lado, la infusión de hojas secas y el licuado de la pulpa fueron los que mostraron una mayor inhibición contra la cepa de Staphylococcus spp. en el ensayo de actividad antibacteriana. Conclusión: Las hojas secas de Chrysobalanus icaco mostraron alto contenido de polifenoles, asociado a su potencial actividad antioxidante y antibacteriana. Además, se aportaron nuevos datos de composición química de la semilla, se observó que los azúcares detectados inicialmente en la semilla inmadura se pierden considerablemente con la maduración del fruto.


Introduction: Chrysobalanus icaco L. (Chrysobalanaceae) is a shrub used in Latin American traditional phytotherapy, but in the province of Chiriquí its fruit has been reported to be used in food preserves, not for medicinal purposes. Objective: Characterize the secondary metabolites present in Chrysobalanus icaco leaves and seeds and evaluate their in vitro biological activity. Methods: The secondary metabolites present in extracts from leaves and immature and mature seeds of icaco were detected by phytochemical screening and purification with chromatographic techniques. Evaluation was then conducted of total polyphenolic content and total antioxidant activity of the leaf, seed and pulp infusion as well as its antibacterial activity in vitro. Results: Phytochemical screening of the leaves found flavonoids, cardiotonic glycosides, triterpenes and steroids. Sugar mixtures were the most abundant components in immature seeds, whereas fatty acids were found in the endocarp (almond) of mature seeds. Total polyphenolic data about icaco extracts showed high contents of these metabolites in the dry leaf infusion. DPPH radical inhibition was also greater for icaco dry leaves, followed by immature leaf infusion. The dry leaf infusion and the pulp shake displayed the greatest inhibition against the Staphylococcus spp. strain in the antibacterial activity test. Conclusion: Icaco dry leaves exhibited a high polyphenolic content, associated to their antioxidant and antibacterial activity. Fresh data were also contributed about the chemical composition of the seed. It was observed that the sugars initially detected in immature seeds are considerably lost as the fruit ripens.


Assuntos
Chrysobalanaceae , Compostos Fitoquímicos , Antibacterianos , Antioxidantes , Técnicas In Vitro , Medicina Tradicional
4.
J Ethnopharmacol ; 131(2): 497-501, 2010 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-20600752

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Cecropia obtusifolia (Cecropiaceae) and Psychotria poeppigiana (Synonym: Cephaelis elata, Rubiaceae) are two Latin American plants broadly used in traditional Amerindian medicine. The former, together with many other species of the genus Cecropia, share the folk reputation of curing heart failure, cough, asthma and bronchitis. The latter is used in Panama by Kuna and Ngäbe Buglé (Guaymies) native Indians for the treatment of dyspnea. AIM OF THE STUDY: Based on screening of selected medicinal Panamanian plants by radioligand-binding techniques by Caballero-George et al. (2001), the present study was carried out in order to investigate the vasoactive effects of different fractions from both P. poeppigiana and C. obtusifolia on rat thoracic aorta and identify active fractions and their chemical constituents. MATERIALS AND METHODS: Both acid and neutral methanol fractions (P-AMeOH and P-NMeOH) and acid and neutral dichlorometane fractions (P-ADCM and P-NDCM) were obtained from P. poeppigiana crude methanolic and dichlorometane extracts, respectively. Identical fractionation was carried out for C. obtusifolia (C-AMeOH, C-NMeOH, C-ADCM and C-NDCM. Vasorelaxant effect of all fractions, and their inhibition of contractile responses to angiotensin II were evaluated in isolated aortic rings. RESULTS: P-AMeOH, P-NMeOH and P-ADCM fractions induced a concentration-dependent relaxation (43.9+/-1.8%, 35.3+/-4.7% and 52.9+/-3.5%, respectively) in the endothelium-intact aorta precontracted by phenylephrine (PE, 10(-6)M). The relaxation produced by C-AMeOH and C-NMeOH (57.3+/-2.5% and 53.3+/-3.3%, respectively) was greater than the effect produced by C-ADCM and C-NDCM (42.2+/-3.4% and 21.8+/-0.8%, respectively). Only the incubation of the aortic rings with P-AMeOH reduced the maximum contraction induced by angiotensin II at 20.08+/-0.55%. CONCLUSIONS: The direct vasorelaxation effect observed could explain in part the ethnomedical use of these plants in Amerindian traditional medicine. The most active fractions contain phenolic and aromatic acid compounds. Furthermore, P-AMeOH, the only fraction that showed both vasorelaxant effect and inhibition of contractile responses to angiotensin II, is the most rich in aromatic acids compounds and the only one that contains scopoletin.


Assuntos
Cecropia (Planta)/química , Contração Muscular/efeitos dos fármacos , Músculo Liso Vascular/efeitos dos fármacos , Extratos Vegetais/farmacologia , Psychotria/química , Vasodilatação/efeitos dos fármacos , Vasodilatadores/farmacologia , Angiotensina II/farmacologia , Animais , Aorta Torácica/efeitos dos fármacos , Relação Dose-Resposta a Droga , Etnofarmacologia , Humanos , Índios Centro-Americanos , Masculino , Medicina Tradicional , Panamá , Componentes Aéreos da Planta , Extratos Vegetais/química , Ratos , Ratos Endogâmicos SHR , Ratos Sprague-Dawley , Vasoconstritores/farmacologia
5.
J Ethnopharmacol ; 124(1): 159-61, 2009 Jul 06.
Artigo em Inglês | MEDLINE | ID: mdl-19537297

RESUMO

ETHNOPHARMACOLOGICAL RELEVANCE: Dimerocostus strobilaceus is used by the Kuna Indians of Panama for the treatment of hypertension and other cardiovascular diseases. AIM OF THE STUDY: We investigated the vascular effects of acid and neutral fractions obtained from methanol and dichloromethane extracts of Dimerocostus strobilaceus. MATERIALS AND METHODS: The acid and neutral methanol fractions (A-MeOH and N-MeOH) or acid and neutral dichlorometanic fractions (A-DCM and N-DCM) were tested using isolated rat aortic rings with or without endothelium pre-contracted by phenylephrine. We examined the ability of these different fractions at different concentrations to modify vascular responses induced by angiotensin II using endothelium-denuded aortic rings from Spontaneously Hypertensive Rats (SHR). RESULTS: In aortic rings with intact endothelium A-MeOH, N-MeOH and A-DCM fractions produced a concentration-dependent vasorelaxation (62.4 +/- 5.2, 64.5 +/- 5.0 and 63.7 +/- 5.0%, respectively), whereas the N-DCM fraction did not produce any vasorelaxant effect. Maximal relaxation evocated by vasoactive fractions was substantially inhibited on aortic rings without endothelium.Our study demonstrates that A-MeOH, N-MeOH, A-DCM and N-DCM significantly reduce contractile responses induced by angiotensin-II on aortic rings. CONCLUSIONS: Our findings may contribute to a better understanding of the potential link between vascular properties observed with Dimerocostus strobilaceus and their ethnobotanical use.


Assuntos
Endotélio/efeitos dos fármacos , Magnoliopsida , Extratos Vegetais/farmacologia , Vasoconstrição/efeitos dos fármacos , Vasodilatação/efeitos dos fármacos , Vasodilatadores/farmacologia , Angiotensina II , Animais , Aorta , Relação Dose-Resposta a Droga , Concentração de Íons de Hidrogênio , Masculino , Panamá , Fenilefrina , Ratos , Ratos Endogâmicos SHR , Ratos Sprague-Dawley , Vasoconstritores/farmacologia
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