000Synthesis of new α-aminophosphonates: Evaluation as anti-inflammatory agents and QSAR studies.
Bioorg Med Chem
; 27(12): 2376-2386, 2019 06 15.
Article
en En
| MEDLINE
| ID: mdl-30635220
In this paper, we report the synthesis of a new series of α-aminophosphonates derivatives based in an efficient three-component reaction. All compounds prepared showed significant anti-inflammatory activity, being the compounds 1a, 1c, 1d, 1f, 2b and 2c the most promising ones, in terms of maximal efficacy (over 95%), potency (ED50 range between 0.7 and 10.1â¯mg/ear) and relative potency (range from 0.04 to 0.67). Compounds 1a, 1c, 1d and 1f significantly decrease the number of neutrophils (range from 46.7 to 63.0%) and monocytes (18.9-34.1%) in blood samples from the orbital sinus. Additionally, QSAR model revealed that the spherical molecular shape and the location of the HOMO on the phenyl ring improves the anti-inflammatory activity of the compounds. The values of R2, Q2, s and F statistical parameters and the QUIK, asymptotic Q2 and Overfitting rules validate the descriptive and predictive ability of the QSAR model. Altogether these results suggest that these new α-aminophosphonates are potential agents for the treatment of inflammation.
Palabras clave
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Relación Estructura-Actividad Cuantitativa
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Etanolaminas
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Organofosfonatos
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Inflamación
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Antiinflamatorios
Tipo de estudio:
Evaluation_studies
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Prognostic_studies
Límite:
Animals
Idioma:
En
Revista:
Bioorg Med Chem
Asunto de la revista:
BIOQUIMICA
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QUIMICA
Año:
2019
Tipo del documento:
Article
País de afiliación:
México