dc.creator | Chavez M.I. | |
dc.creator | Soto M. | |
dc.creator | Cimino F.A. | |
dc.creator | Olea A.F. | |
dc.creator | Espinoza L. | |
dc.creator | Díaz K. | |
dc.creator | Taborga L. | |
dc.date.accessioned | 2020-09-02T22:14:51Z | |
dc.date.accessioned | 2022-11-08T20:25:28Z | |
dc.date.available | 2020-09-02T22:14:51Z | |
dc.date.available | 2022-11-08T20:25:28Z | |
dc.date.created | 2020-09-02T22:14:51Z | |
dc.date.issued | 2018 | |
dc.identifier | 19, 6, - | |
dc.identifier | 16616596 | |
dc.identifier | https://hdl.handle.net/20.500.12728/4016 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/5145675 | |
dc.language | en | |
dc.publisher | MDPI AG | |
dc.subject | Antifungal activity | |
dc.subject | Fungicide | |
dc.subject | Geranylated phenols | |
dc.subject | Oomycetes | |
dc.subject | Phytophthora cinnamomi | |
dc.subject | (e) 2 (3,7 dimethylocta 2,6 dienyl) 3,4,5 trimethoxyphenol | |
dc.subject | (e) 2 (3,7 dimethylocta 2,6 dienyl) 6 methoxyphenol | |
dc.subject | (e) 3 (3,7 dimethylocta 2,6 dienyl) 2 methoxyphenol | |
dc.subject | (e) 3 (3,7 dimethylocta 2,6 dienyl)benzene 1,2 diol | |
dc.subject | (e) 4 (3,7 dimethylocta 2,6 dienyl) 2,3 dimethoxyphenol | |
dc.subject | (e) 4 (3,7 dimethylocta 2,6 dienyl)benzene 1,2 diol | |
dc.subject | (e) 4 (3,7 dimethylocta 2,6 dienyl)benzene 1,3 diol | |
dc.subject | (e) 5 (3,7 dimethylocta 2,6 dienyl) 2 methoxyphenol | |
dc.subject | (e) 5 (3,7 dimethylocta 2,6 dienyl)benzene 1,2,4 triol | |
dc.subject | (e) 6 (3,7 dimethylocta 2,6 dienyl) 2,3 dimethoxyphenol | |
dc.subject | 2,4 bis((e) 3,7 dimethylocta 2,6 dienyl)benzene 1,3 diol | |
dc.subject | 2,6 bis((e) 3,7 dimethylocta 2,6 dienyl) 3,4,5 trimetoxyphenol | |
dc.subject | 4,5 bis((e) 3,7 dimethylocta 2,6 d ienyl) 2 methoxyphenol | |
dc.subject | 4,5 bis((e) 3,7 dimethylocta 2,6 dienyl)benzene 1,2 diol | |
dc.subject | 4,6 bis((e) 3,7 dimethylocta 2,6 dienyl)benzene 1,3 diol | |
dc.subject | catechol | |
dc.subject | geraniol | |
dc.subject | geranylated phenol | |
dc.subject | phenol | |
dc.subject | unclassified drug | |
dc.subject | antifungal agent | |
dc.subject | phenol derivative | |
dc.subject | antifungal activity | |
dc.subject | Article | |
dc.subject | Botrytis cinerea | |
dc.subject | controlled study | |
dc.subject | growth inhibition | |
dc.subject | nonhuman | |
dc.subject | nuclear magnetic resonance spectroscopy | |
dc.subject | Phytophthora cinnamomi | |
dc.subject | chemistry | |
dc.subject | growth, development and aging | |
dc.subject | Phytophthora | |
dc.subject | synthesis | |
dc.subject | Antifungal Agents | |
dc.subject | Phenols | |
dc.subject | Phytophthora | |
dc.title | In vitro antifungal activity of new and known geranylated phenols against Phytophthora cinnamomi rands | |
dc.type | Article | |