Sabrina França Silva
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Sabrina França Silva has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
Daniel Crístian Ferreira Soares
Laboratório de Bioengenharia Universidade Federal de Itajubá, Rua Irmã Ivone Drumond, 200, Distrito Industrial II 35903-087 Itabira-MG Brazil
1 shared publication- Diogo Montes Vidal
Departamento de Química Instituto de Ciências Exatas Universidade Federal de Minas Gerais Belo Horizonte Minas Gerais Brazil
1 shared publication - Elizabeth Luciana Marinho Miguel
Departamento de Química Instituto de Ciências Exatas Universidade Federal de Minas Gerais Avenida Presidente Antônio Carlos, 6627 Pampulha 31270-901 Belo Horizonte-MG Brazil
1 shared publication Grasiely Faria de Sousa
Departamento de Química Instituto de Ciências Exatas Universidade Federal de Minas Gerais Avenida Presidente Antônio Carlos, 6627 Pampulha 31270-901 Belo Horizonte-MG Brazil
1 shared publication- Kamila Thomaz Oliveira
Departamento de Microbiologia Instituto de Ciências Biológicas Universidade Federal de Minas Gerais Avenida Presidente Antônio Carlos, 6627 Pampulha 31270-901 Belo Horizonte-MG Brazil
1 shared publication - Lucienir Pains Duarte
Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, Avenida Presidente Antônio Carlos, 6627, Pampulha, Belo Horizonte 31270-901, MG, Brazil
1 shared publication
Latest Publications
- 21 September 2023
- Published by Wiley in Chemistry & Biodiversity
- Vol. 20 (10) , e202301207
Evaluation of Cytotoxicity and Antifungal Activity of Friedelanes from Salacia elliptica Roots
Plants from Salacia genus are used in traditional medicine for a wide range of diseases. Previous studies reported bioactive pentacyclic triterpenoids from S. elliptica leaves and branches. In this study, the novel pentacyclic triterpenoid 7α,15α‐dihydroxyfriedelan‐3‐one (1) was obtained from the roots of Salacia elliptica, along with seven known compounds: friedelan‐3‐one (2), friedelan‐3β‐ol (3), friedelan‐1,3‐dione (4), friedelan‐3,15‐dione (5), 15α‐hydroxyfriedelan‐3‐one (6), 15α,26‐dihydroxyfriedelan‐3‐one (7), and 26‐hydroxyfriedelan‐3,15‐dione (8). Additionally, one steroid, spinasterol (9), was also identified. The chemical structures of all compounds were established through 1H and 13C‐NMR. Compound 1 was analysed by additional 2D experiments (HMBC, HSQC, COSY, and NOESY) for complete elucidation. Furthermore, the cytotoxicity of compounds 2, 3, 6, 7 and 8 against the A549 lung cancer cells model was evaluated. The flow cytometry analysis revealed a significant cytotoxic activity similar to that exhibited by the triterpenoid lupeol. Additionally, compounds 2, 3, 6, and 7 were tested for in vitro antifungal activity against Candida, Cryptococcus and Sporothrix strains. However, all compounds showed no activity at the tested concentrations.
- 21 September 2023
- Published by Wiley in Chemistry & Biodiversity
- Vol. 20 (10) , e202301207
Evaluation of Cytotoxicity and Antifungal Activity of Friedelanes from Salacia elliptica Roots
Plants from Salacia genus are used in traditional medicine for a wide range of diseases. Previous studies reported bioactive pentacyclic triterpenoids from S. elliptica leaves and branches. In this study, the novel pentacyclic triterpenoid 7α,15α‐dihydroxyfriedelan‐3‐one (1) was obtained from the roots of Salacia elliptica, along with seven known compounds: friedelan‐3‐one (2), friedelan‐3β‐ol (3), friedelan‐1,3‐dione (4), friedelan‐3,15‐dione (5), 15α‐hydroxyfriedelan‐3‐one (6), 15α,26‐dihydroxyfriedelan‐3‐one (7), and 26‐hydroxyfriedelan‐3,15‐dione (8). Additionally, one steroid, spinasterol (9), was also identified. The chemical structures of all compounds were established through 1H and 13C‐NMR. Compound 1 was analysed by additional 2D experiments (HMBC, HSQC, COSY, and NOESY) for complete elucidation. Furthermore, the cytotoxicity of compounds 2, 3, 6, 7 and 8 against the A549 lung cancer cells model was evaluated. The flow cytometry analysis revealed a significant cytotoxic activity similar to that exhibited by the triterpenoid lupeol. Additionally, compounds 2, 3, 6, and 7 were tested for in vitro antifungal activity against Candida, Cryptococcus and Sporothrix strains. However, all compounds showed no activity at the tested concentrations.