Bernthsen synthesis, antimicrobial activities and cytotoxicity of acridine derivatives
- Author
- PATEL, Mehul M1 ; MALI, Mimansha D1 ; PATEL, Saurabh K1
[1] Chemistry Research laboratory, Department of Chemistry, Veer Narmad South Gujarat University, Surat 395 007, Gujarat, India - Source
Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 21, pp 6324-6326, 3 p ; ref : 17 ref
- ISSN
- 0960-894X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier, Amsterdam
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Author keyword
- 4-(Acridin-9-ylmethyl)-2H-(substituted chromen)-2-one Antibacterial activity Anticancer activity Antifungal activity
- Keyword (fr)
- Antibactérien Anticancéreux Antifongique Antimicrobien Aspergillus niger Cellule tumorale Composé aromatique Composé tricyclique Cytotoxicité Dérivé de l'acridine Dérivé de la coumarine Embryon Escherichia coli Homme Hétérocycle azote Hétérocycle oxygène In vitro Lactone Larynx Leucémie promyélocytaire Lignée HL60 Lignée cellulaire Phénols Pseudomonas aeruginosa Rein Relation structure activité Staphylococcus aureus Synthèse chimique Lignée HEK293 Lignée HEP2 Synthèse Bernthsen Bactérie Chlore Composé organique Enterobacteriaceae Fungi Imperfecti Fungi Micrococcaceae Micrococcales Pseudomonadaceae Pseudomonadales
- Keyword (en)
- Antibacterial agent Antineoplastic agent Antifungal agent Antimicrobial agent Aspergillus niger Tumor cell Aromatic compound Tricyclic compound Cytotoxicity Acridine derivatives Coumarine derivatives Embryo Escherichia coli Human Nitrogen heterocycle Oxygen heterocycle In vitro Lactone Larynx Promyelocytic leukemia HL60 cell line Cell line Phenols Pseudomonas aeruginosa Kidney Structure activity relation Staphylococcus aureus Chemical synthesis Bacteria Chlorine Organic compounds Enterobacteriaceae Fungi Imperfecti Fungi Micrococcaceae Micrococcales Pseudomonadaceae Pseudomonadales
- Keyword (es)
- Antibacteriano Anticanceroso Antifúngico Antimicrobiano Aspergillus niger Célula tumoral Compuesto aromático Compuesto tricíclico Citotoxicidad Acridina derivado Embrión Escherichia coli Hombre Heterociclo nitrógeno Heterociclo oxígeno In vitro Lactona Laringe Leucemia promielocítica Línea HL60 Línea celular Fenoles Pseudomonas aeruginosa Riñón Relación estructura actividad Staphylococcus aureus Síntesis química Bacteria Cloro Compuesto orgánico Enterobacteriaceae Fungi Imperfecti Fungi Micrococcaceae Micrococcales Pseudomonadaceae Pseudomonadales
- 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
- 23419264
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.bmcl.2010.06.001 
https://dx.doi.org/10.1016/j.bmcl.2010.06.001
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