Synthesis and characterization of new types of halogenated and alkylated imidazolidineiminothiones and a comparative study of their antitumor, antibacterial, and antifungal activities
- Author
- MOUSSA, Ziad1 ; EL-SHARIEF, Marwa A. M. Sh2 ; EL-SHARIEF, Ahmed M. Sh3
[1] Department of Chemistry, Faculty of Science, Taibah University, P.O. Box 30002, Almadinah Almunawarrah, Saudi Arabia
[2] Applied Organic Chemistry Department, National Research Center, Dokki, Cairo, Egypt
[3] Department of Chemistry, Faculty of Science, Al-Azhar University, Nasr City, Cairo, Egypt - Source
European journal of medicinal chemistry. 2011, Vol 46, Num 6, pp 2280-2289, 10 p ; ref : 74 ref
- CODEN
- EJMCA5
- ISSN
- 0223-5234
- Scientific domain
- Organic chemistry; Pharmacology drugs
- Publisher
- Elsevier, Kidlington
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- Alkylated imidazolidineiminothiones Antifungal Antimicrobial Antitumor Halogenated imidazolidineiminothiones N-Arylcyanothioformanilides
- Keyword (fr)
- Antibactérien Anticancéreux Antifongique Antimicrobien Aspergillus flavus Bacillus subtilis Candida albicans Cellule tumorale Cycle 5 chaînons Cytotoxicité Dérivé du benzène Escherichia coli Etude comparative Homme Hétérocycle azote In vitro Lignée cellulaire Relation structure activité Sarcina Staphylococcus aureus Synthèse chimique Imidazolidin-2-one(1,3-diaryl-4-imino-5-thioxo) Sarcina lutea Bacillaceae Bacillales Bactérie Enterobacteriaceae Eubacteriales Fungi Imperfecti Fungi Halogène Composé organique Micrococcaceae Micrococcales Peptococcaceae
- Keyword (en)
- Antibacterial agent Antineoplastic agent Antifungal agent Antimicrobial agent Aspergillus flavus Bacillus subtilis Candida albicans Tumor cell Five membered ring Cytotoxicity Benzene derivatives Escherichia coli Comparative study Human Nitrogen heterocycle In vitro Cell line Structure activity relation Sarcina Staphylococcus aureus Chemical synthesis Bacillaceae Bacillales Bacteria Enterobacteriaceae Eubacteriales Fungi Imperfecti Fungi Halogen Organic compounds Micrococcaceae Micrococcales Peptococcaceae
- Keyword (es)
- Antibacteriano Anticanceroso Antifúngico Antimicrobiano Aspergillus flavus Bacillus subtilis Candida albicans Célula tumoral Ciclo 5 eslabones Citotoxicidad Benceno derivado Escherichia coli Estudio comparativo Hombre Heterociclo nitrógeno In vitro Línea celular Relación estructura actividad Sarcina Staphylococcus aureus Síntesis química Bacillaceae Bacillales Bacteria Enterobacteriaceae Eubacteriales Fungi Imperfecti Fungi Halógeno Compuesto orgánico Micrococcaceae Micrococcales Peptococcaceae
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02R Antineoplastic agents / 002B02R01 General aspects
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02S Antibiotics. Antiinfectious agents. Antiparasitic agents / 002B02S01 General aspects
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02S Antibiotics. Antiinfectious agents. Antiparasitic agents / 002B02S02 Antibacterial agents
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02S Antibiotics. Antiinfectious agents. Antiparasitic agents / 002B02S04 Antifungal agents
- Discipline
- Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 24170610
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.ejmech.2011.03.009 
https://dx.doi.org/10.1016/j.ejmech.2011.03.009
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