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dc.contributor.authorCosta, Renyer A.
dc.contributor.authorda Silva, Jonathas Nunes [UNESP]
dc.contributor.authorOliveira, Kelson M. T.
dc.contributor.authorDutra, Lívia M.
dc.contributor.authorCosta, Emmanoel V.
dc.date.accessioned2020-12-12T01:13:07Z
dc.date.available2020-12-12T01:13:07Z
dc.date.issued2020-06-01
dc.identifierhttp://dx.doi.org/10.1007/s11224-020-01491-2
dc.identifier.citationStructural Chemistry, v. 31, n. 3, p. 1223-1243, 2020.
dc.identifier.issn1572-9001
dc.identifier.issn1040-0400
dc.identifier.urihttp://hdl.handle.net/11449/198448
dc.description.abstractDiterpenes are a class of secondary metabolites that attract much attention due to the numerous biological activities presented, such as antimicrobial, antiviral, hypoglycemic, larvicidal, and antitumor. In the present study, four ent-kaurane diterpenes isolated from Annona vepretorum were analyzed through a DFT theoretical approach using the B3LYP exchange-correlation functional with 6-311G (2d, p) basis set, which allowed to obtain optimized geometry of the structures, highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO), MEPS analysis, and vibrational wavenumbers. The analysis of the HOMO-LUMO energy gaps and reactive descriptor indices values allowed us to verify that the structures present a differentiated reactivity, indicating a differentiated activity. The comparative IR studies, allied to potential energy distribution calculation, revealed several characteristic vibrations that characterize the ent-kaurane skeleton, besides enabling the existence of intermolecular H-bonds through dimers formation. By molecular dynamic simulations, the interactions between diterpenes atoms and water, methanol, and chloroform were simulated, which enable us to analyze the stability of the studied structures in different solvated media and the best sites to form H-bonds. In addition, the stability of intramolecular H-bonds was evaluated. Guided by the in vitro cytotoxicity presented by the investigated diterpenes, molecular docking calculations were performed with the key enzymes NR3C1 and with rat-type II adenylyl cyclase C2 (ACC2) domain, revealing good interactions with the active site of the tested enzymes, justifying the previous experimental results.en
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFinanciadora de Estudos e Projetos
dc.format.extent1223-1243
dc.language.isoeng
dc.relation.ispartofStructural Chemistry
dc.sourceScopus
dc.subjectDFT
dc.subjectent-Kaurane diterpenes
dc.subjectMolecular docking
dc.subjectMolecular dynamics
dc.titleQuantum chemical studies, vibrational analysis, molecular dynamics and docking calculations of some ent-kaurane diterpenes from Annona vepretorum: a theoretical approach to promising anti-tumor moleculesen
dc.typeArtigo
dc.contributor.institutionFederal University of Amazonas (DQ-UFAM)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionFederal University of Vale do São Francisco
dc.description.affiliationDepartment of Chemistry Federal University of Amazonas (DQ-UFAM)
dc.description.affiliationFaculty of Sciences and Letters - Araraquara Campus São Paulo State University (UNESP)
dc.description.affiliationMedicinal Plant Studies and Research Center Federal University of Vale do São Francisco
dc.description.affiliationUnespFaculty of Sciences and Letters - Araraquara Campus São Paulo State University (UNESP)
dc.identifier.doi10.1007/s11224-020-01491-2
dc.identifier.scopus2-s2.0-85078483890
unesp.author.orcid0000-0002-9699-0891[1]
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