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pro vyhledávání: '"João M, Batista"'
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Autor:
Patricia Sartorelli, João M. Batista, Jackson Monteiro, Luiz Felipe D. Passero, Jéssica A. Jesus, Márcia D. Laurenti, João H. G. Lago, Marisi G. Soares, Andrea N. L. Batista
Publikováno v:
Current Topics in Medicinal Chemistry. 22:1626-1633
Background: The fractionation of the n-hexane phase of the EtOH extract from the leaves of Duguetia lanceolata (Annonaceae) led to the identification of the sesquiterpene (–)-cyclocolorenone. Objective: Chemical characterization, including determin
Autor:
Carson Wiethan, Ingredy B. Braga, Vitor H. Menezes da Silva, João M. Batista, Carlos Roque D. Correia
Publikováno v:
ChemCatChem.
Autor:
Tom Vermeyen, Andrea N. L. Batista, Alessandra L. Valverde, Wouter Herrebout, João M. Batista
Publikováno v:
Physical chemistry, chemical physics
Vibrational circular dichroism (VCD) is one of the most powerful techniques to assess stereochemistry of chiral molecules in solution state. The need for quantum chemical calculations to interpret experimental data, however, has precluded its widespr
Autor:
Lhaís Araújo Caldas, Mariana T. Rodrigues, Andrea N. L. Batista, João M. Batista, João H. G. Lago, Marcelo J. P. Ferreira, Ileana G. S. Rubio, Patricia Sartorelli
Publikováno v:
Molecules, Vol 25, Iss 13, p 3005 (2020)
This work describes the chromatographic fractionation of the aerial parts of Calea pinnatifida and the structural characterization and determination of the absolute configuration of the isolated compounds as well as their antitumor potential. The HPL
Externí odkaz:
https://doaj.org/article/6de0a8a91fdd4765863317059da008e3
Publikováno v:
Revista Brasileira de Farmacognosia. 31:612-624
The determination of the absolute configuration of chiral bioactive natural products is a crucial step in their structural characterization. Several well-established techniques, such as X-ray crystallography, stereo-controlled organic synthesis, NMR,
Autor:
Fernanda F. Camilo, Andre G. Tempone, Andrea N. L. Batista, João Henrique G. Lago, Larissa V.F. Oliveira, Vinicius S. Londero, João M. Batista, João Batista Baitello, Guilherme Medeiros Antar, Thais A. Costa-Silva
Publikováno v:
Journal of Natural Products. 84:1489-1497
Twigs of Nectandra barbellata were extracted using a solution of the ionic liquid 1-butyl-3-methylimidazolium bromide (BMImBr) in H2O, assisted by microwave (MAE). After successive chromatographic steps, one sesquiterpene, costic acid, and three new
Autor:
Jackson, Monteiro, Luiz Felipe D, Passero, Jéssica A, Jesus, Márcia D, Laurenti, João H G, Lago, Marisi G, Soares, Andrea N L, Batista, João M, Batista, Patricia, Sartorelli
Publikováno v:
Current topics in medicinal chemistry. 22(19)
The fractionation of the n-hexane phase of the EtOH extract from the leaves of Duguetia lanceolata (Annonaceae) led to the identification of the sesquiterpene (-)-cyclocolorenone.Chemical characterization, including determination of the absolute ster
Autor:
Andrea N. L. Batista, Francisco A. Marques, Sirlei Dias Teixeira, Ana Paula P K Hendges, Vanderlei Aparecido de Lima, Beatriz Helena L. N. Sales Maia, João M. Batista, Michelangelo Muzell Trezzi, Francielli S. Santana, Elaine Fernanda Dos Santos
Publikováno v:
Journal of Natural Products. 83:3511-3518
Five new neocassane-like diterpenes (1-5) were isolated from the roots of Eragrostis plana. Their structures were elucidated by spectroscopic data, and the absolute configurations of the representative compounds neocassa-12(17),15-dien-3-one (2) and
Autor:
Fernando M. dos Santos, Leila Gimenes, Liany Luna-Dulcey, João M. Batista, Cecília Patrícia Popolin, João B. Fernandes, Márcia Regina Cominetti, Dan Staerk
Publikováno v:
Journal of Natural Products. 83:1859-1875
In this study, HPLC-PDA-HRMS-SPE-NMR data were used for initial analysis of the CH2Cl2 fraction of an EtOH extract of the leaves of Picramnia glazioviana. The HRMS, UV, and NMR data obtained from the HPLC-PDA-HRMS-SPE-NMR analysis were used to direct