Literature DB >> 18191402

Synthesis and in silico biological activity evaluation of new N-substituted pyrazolo-oxazin-2-one systems.

Nora Benaamane1, Bellara Nedjar-Kolli, Yamina Bentarzi, Lamouri Hammal, Athina Geronikaki, Phaedra Eleftheriou, Alexey Lagunin.   

Abstract

Cyclisation of pyrazolo-beta-enaminones 3 readily obtained from 4-aceto acetyl pyrazol 2 with triphosgene led to the formation of N-substituted pyrazolo-1,3-oxazin-2-ones 4 in good yields. Estimation of pharmacotherapeutic potential, possible molecule mechanisms of action, toxic/side effects and interaction with drug-metabolizing enzymes were made for synthesised compounds on the basis of prediction of activity spectra for substances (PASS) prediction results and their analysis by PharmaExpert software. COX inhibition predicted by PASS was confirmed by experimental evaluation.

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Year:  2007        PMID: 18191402     DOI: 10.1016/j.bmc.2007.12.033

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  3 in total

1.  Computer-aided discovery of biological activity spectra for anti-aging and anti-cancer olive oil oleuropeins.

Authors:  Bruna Corominas-Faja; Elvira Santangelo; Elisabet Cuyàs; Vicente Micol; Jorge Joven; Xavier Ariza; Antonio Segura-Carretero; Jordi García; Javier A Menendez
Journal:  Aging (Albany NY)       Date:  2014-09       Impact factor: 5.682

2.  Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products.

Authors:  Sultan Taskaya; Nurettin Menges; Metin Balci
Journal:  Beilstein J Org Chem       Date:  2015-05-28       Impact factor: 2.883

3.  Facile cleavage of C-C bond: conversion of pyrane derivative to 1,3-oxazin derivative.

Authors:  Zhilan Lin; Xueli Zhang; Xinkui You; Yuan Gao
Journal:  Tetrahedron       Date:  2012-05-30       Impact factor: 2.457

  3 in total

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