Rachid Touzani

Dr. Rachid Touzani

Chemistry, Université Mohammed Premier, Oujda, Morocco
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2020 in Arabian Journal of Chemistry
Verified
Journal Article
Open access
NANadia Arrousse
Nadia Arrousse
RSR. Salim
R. Salim
YKYassine KADDOURI
Yassine KADDOURI
AZAbdelkader Zarrouk
Abdelkader Zarrouk
DZD. Zahri
D. Zahri
SJS. Jodeh
S. Jodeh

1 October 2007 in Materials Chemistry and Physics
Verified
Journal Article
Closed access
MBM. Benabdellah
M. Benabdellah
Rachid TouzaniRachid Touzani
Rachid Touzani
AAA. Aouniti
A. Aouniti
ADA. Dafali
A. Dafali
SKS. El Kadiri
S. El Kadiri
MBM. Benkaddour
M. Benkaddour

1 January 2020 in Heliyon
Verified
Journal Article
Open access
YKYassine KADDOURI
Yassine KADDOURI
FAFarid Abrigach
Farid Abrigach
EYEl Bekaye Yousfi
El Bekaye Yousfi
MKMohamed EL KODADI
Mohamed EL KODADI
Rachid TouzaniRachid Touzani
Rachid Touzani
Novel heterocyclic compounds containing pyrazole, thiazole and pyridine moieties were designed and prepared based on the condensation reaction between 1,3-thiazole or aminopyridine derivatives and 1H-pyrazole,3,5-dimethyl-1H-pyrazole or 1,2,4-triazole. Their structures were confirmed with FTIR, 1H and 13C NMR analyses. DPPH scavenging assay was used to evaluate their antioxidant potential. The ligand 4 showed the best antioxidant activity with an IC50 = 4.67 μg/mL, while IC50 values of the other compounds were found to be ranging from 20.56 to 45.32 μg/mL. DFT and molecular docking studies were performed in order to gain better insights and to understand the relationship between the structures of the studied compounds and their antioxidant activities. The results obtained revealed a good agreement between the experimental and the theoretical findings.

1 November 2019 in Journal of Molecular Structure
Verified
Journal Article
Closed access
MKM. Khattabi
M. Khattabi
Fouad BenhibaFouad Benhiba
Fouad Benhiba
STS. Tabti
S. Tabti
ADA. Djedouani
A. Djedouani
AAA. El Assyry
A. El Assyry
AZA. Zarrouk
A. Zarrouk

30 August 2002 in Molecules
Verified
Journal Article
Open access
PDF file
MWMichael J. Waring
Michael J. Waring
THTaibi Ben Hadda
Taibi Ben Hadda
AKAnn T. Kotchevar
Ann T. Kotchevar
ARAbdelkrim Ramdani
Abdelkrim Ramdani
Rachid TouzaniRachid Touzani
Rachid Touzani
TETom Ellis
Tom Ellis
A variety of 2,3-bifunctionalized quinoxalines (6-14) have been prepared by the condensation of 1,6-disubstituted-hexan-1,3,4,6-tetraones (1-4) with o-phenylenediamine, (R,R)-1,2-diaminocyclohexane and p-nitro-o-phenylenediamine. It is concluded that strong intramolecular N-H----O bonds in the favoured keto-enamine form may be responsible for the minimal biological activities observed in DNA footprinting, antitubercular, anti-fungal and anticancer tests with these hyper π-conjugated quinoxaline derivatives. However, subtle alteration by addition of a nitro group affecting the charge distribution confers significant improvements in biological effects and binding to DNA.

1 February 2007 in Materials Letters
Verified
Journal Article
Closed access
MBM. Benabdellah
M. Benabdellah
Rachid TouzaniRachid Touzani
Rachid Touzani
ADA. Dafali
A. Dafali
Belkheir HammoutiBelkheir Hammouti
Belkheir Hammouti
SKS. El Kadiri
S. El Kadiri