Comparative analysis of the trypanocidal activity and chemical properties of E-lychnophoric acid and its derivatives using theoretical calculations
Fuente:
Redalyc
Saved in:
| Main Author: | |
|---|---|
| Format: | Artículo científico |
| Language: | en |
| Published: |
Universidade Estadual Paulista Júlio de Mesquita Filho
2005
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1876473298112479232 |
|---|---|
| author | A. F. C. Alcântara |
| author_facet | A. F. C. Alcântara |
| contents | Comparative analysis of the trypanocidal activity and chemical properties of E-lychnophoric acid and its derivatives using theoretical calculations A. F. C. Alcântara E. Chiari A. B. Oliveira J. E. Guimarães D. Silveira D. S. Raslan Química DFT calculation Trypanosoma cruzi Lychnophora pinaster trypanocidal activity caryophyllene derivatives E-Lychnophoric acid 1, its derivative ester 2 and alcohol 3 killed 100% of trypomastigoteblood forms of Trypanosoma cruzi at the concentrations of 13.86, 5.68, and 6.48 µg/mL, respectively.Conformational distribution calculations (AM1) of 1, 2 and 3 gave minimum energies for the conformersa, b, c, and d, which differ from each other only in the cyclononene ring geometry. Calculations (DFT/BLYP/6-31G*) of geometry optimization and chemical properties were performed for conformers of 1, 2,and 3. The theoretical results were numerically compared to the trypanocidal activity. Calculated valuesof atomic charge, orbital population, and vibrational frequencies showed that the C-4C-5 π-endocyclicbond does not affect the trypanocidal activity of the studied compounds. Nevertheless, the structure ofthe group at C-4 strongly influences the activity. However, the theoretical results indicated that the intraring(C-1 and C-9) and π-exocycle (C-8 and C-14) carbons of caryophyllene-type structures promotethe trypanocidal activity of these compounds. 2005 artículo científico 0100-4670 https://www.redalyc.org/articulo.oa?id=42930305 en http://www.redalyc.org/revista.oa?id=429 Eclética Química application/pdf Universidade Estadual Paulista Júlio de Mesquita Filho Eclética Química (Brasil) Num.3 Vol.30 |
| format | Artículo científico |
| id | redalyc_42930305 |
| institution | Redalyc |
| language | en |
| publishDate | 2005 |
| publisher | Universidade Estadual Paulista Júlio de Mesquita Filho |
| spellingShingle | Comparative analysis of the trypanocidal activity and chemical properties of E-lychnophoric acid and its derivatives using theoretical calculations A. F. C. Alcântara Química DFT calculation Trypanosoma cruzi Lychnophora pinaster trypanocidal activity caryophyllene derivatives Comparative analysis of the trypanocidal activity and chemical properties of E-lychnophoric acid and its derivatives using theoretical calculations A. F. C. Alcântara E. Chiari A. B. Oliveira J. E. Guimarães D. Silveira D. S. Raslan Química DFT calculation Trypanosoma cruzi Lychnophora pinaster trypanocidal activity caryophyllene derivatives E-Lychnophoric acid 1, its derivative ester 2 and alcohol 3 killed 100% of trypomastigoteblood forms of Trypanosoma cruzi at the concentrations of 13.86, 5.68, and 6.48 µg/mL, respectively.Conformational distribution calculations (AM1) of 1, 2 and 3 gave minimum energies for the conformersa, b, c, and d, which differ from each other only in the cyclononene ring geometry. Calculations (DFT/BLYP/6-31G*) of geometry optimization and chemical properties were performed for conformers of 1, 2,and 3. The theoretical results were numerically compared to the trypanocidal activity. Calculated valuesof atomic charge, orbital population, and vibrational frequencies showed that the C-4C-5 π-endocyclicbond does not affect the trypanocidal activity of the studied compounds. Nevertheless, the structure ofthe group at C-4 strongly influences the activity. However, the theoretical results indicated that the intraring(C-1 and C-9) and π-exocycle (C-8 and C-14) carbons of caryophyllene-type structures promotethe trypanocidal activity of these compounds. 2005 artículo científico 0100-4670 https://www.redalyc.org/articulo.oa?id=42930305 en http://www.redalyc.org/revista.oa?id=429 Eclética Química application/pdf Universidade Estadual Paulista Júlio de Mesquita Filho Eclética Química (Brasil) Num.3 Vol.30 |
| title | Comparative analysis of the trypanocidal activity and chemical properties of E-lychnophoric acid and its derivatives using theoretical calculations |
| topic | Química DFT calculation Trypanosoma cruzi Lychnophora pinaster trypanocidal activity caryophyllene derivatives |
| url | https://www.redalyc.org/articulo.oa?id=42930305 |