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Design, synthesis, and antitumor activity of new bis-aminomethylnaphthalenes.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2008 Sep 01; Vol. 16 (17), pp. 8003-10. Date of Electronic Publication: 2008 Jul 29. - Publication Year :
- 2008
-
Abstract
- A new series of bis-aminomethylnaphthalenes were synthesized in satisfactory overall yield, through a simple synthetic strategy using reductive amination. The DNA binding properties of these compounds have been examined and compared to those of reference drugs using an UV spectroscopy method. The compounds were evaluated for their in vitro anticancer activity and some of them were studied in vivo. Compound 15 exhibited remarkable antitumor activity and represents a novel template for anticancer chemotherapy and can serve as a new lead compound.
- Subjects :
- Amination
Animals
Antineoplastic Agents chemistry
Binding Sites
Cattle
Cell Cycle drug effects
Cell Line, Tumor
Cell Proliferation drug effects
DNA chemistry
DNA drug effects
DNA Fragmentation drug effects
Drug Screening Assays, Antitumor
Flow Cytometry methods
Humans
Molecular Structure
Naphthalenes chemistry
Spectrophotometry, Ultraviolet methods
Stereoisomerism
Structure-Activity Relationship
Time Factors
Antineoplastic Agents chemical synthesis
Antineoplastic Agents pharmacology
Drug Design
Naphthalenes chemical synthesis
Naphthalenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 16
- Issue :
- 17
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 18715786
- Full Text :
- https://doi.org/10.1016/j.bmc.2008.07.069