Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sadiq Al-Mansury"'
Autor:
Sadiq Al-Mansury, Suhad J. Hadi, Hawraa H. Naji, Adnan M. Jassim, Shatha M. Abbas, Nada Khazal K. Hindi
Publikováno v:
Medical Journal of Babylon, Vol 21, Iss 3, Pp 627-632 (2024)
Background:Tea and coffee have been consumed since decade ago and became a significant part of social life and cultural traditions. Objective:The study aims to evaluate the effects of coffee and black tea extract on some blood factors in adult albino
Externí odkaz:
https://doaj.org/article/2e0c0e4d1ea7406ea0eaf02366274ba1
Autor:
Sadiq Al-Mansury, Mohammed A. Aboktifa, Adnan M Jassim, Asim A. Balakit, Fatin Fadhel Alkazazz
Publikováno v:
Research Journal of Pharmacy and Technology. :224-228
Three 1,2,4-triazole derivatives B, D, and E were evaluated their effect on the activity of antioxidant enzymes glutathione peroxidase (GPX) and superoxide dismutase (SOD) in vivo serum and liver injury in mice that exposed to thioacetamide. Male rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fcbecd5c0043c7181c0a5985225e483
https://doi.org/10.52711/0974-360x.2022.00037
https://doi.org/10.52711/0974-360x.2022.00037
Publikováno v:
Pharmaceutical Chemistry Journal. 55:556-565
Two series of 3-mercapto-1,2,4-triazole derivatives containing alkoxy substituents different in size and position were synthesized and their structures were characterized by FT-IR, 1H NMR, 13C NMR spectroscopy and elemental analysis. The synthesized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::584d12272d315326e05b2fd074f54800
https://doi.org/10.1007/s11094-021-02459-0
https://doi.org/10.1007/s11094-021-02459-0
Synthesis and Anti-Colon Cancer Activity of 1,2,4-Triazole Derivatives with Aliphatic S-Substituents
Publikováno v:
Oriental Journal of Chemistry. 35:77-84
A series of new 3-mercapto-1,2,4-triazoles have been designed, synthesized and their structures were identified by nuclear magnetic resonance (NMR) and Fourier transform infrared (FT-IR) spectrophotometric techniques. The target compounds are designe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::437084eb3a461ba384bbe93af447b9db
https://doi.org/10.13005/ojc/350109
https://doi.org/10.13005/ojc/350109
Publikováno v:
Egyptian Journal of Chemistry.
The first palladium –catalyzed coupling reactions of 1,3,5-triphenyl pyrazoline are reported. The Suzuki-Miyaura reaction of 3-(4-bromophenyl)-1,5-diphenyl pyrazoline with one equivalent of arylboronic acids afforded 3-(biphenyl)-1,5-diphenyl pyraz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::598e4488a1d91f0e23aa9aa2ebfbc9aa
https://doi.org/10.21608/ejchem.2021.57726.3238
https://doi.org/10.21608/ejchem.2021.57726.3238
Autor:
Gamal A. El-Hiti, Mohammed B. Alshammari, Keith Smith, Sadiq Al-Mansury, Asim A. Balakit, Saudi Arabia
Publikováno v:
ResearcherID
ARKIVOC, Vol 2014, Iss 5, Pp 365-375 (2014)
ARKIVOC, Vol 2014, Iss 5, Pp 365-375 (2014)
Lithiation of N'-(2-methylphenyl)-N,N-dimethylurea with three molar equivalents of tert-butyl- lithium at 40 to 30 C takes place on the nitrogen and on the methyl group at position 2 of the phenyl group. The lithium intermediate thus obtaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469a2b1939eed4f98ac5a3c8f6077e15
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000345779400025&KeyUID=WOS:000345779400025
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000345779400025&KeyUID=WOS:000345779400025
