Publication: Copper complexes of 8-aminoquinoline and uracils as novel aromatase inhibitors
Issued Date
2017-08-01
Resource Type
ISSN
1875628X
15701808
15701808
Other identifier(s)
2-s2.0-85027875828
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Mahidol University
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SCOPUS
Bibliographic Citation
Letters in Drug Design and Discovery. Vol.14, No.8 (2017), 880-884
Suggested Citation
Nujarin Sinthupoom, Virapong Prachayasittikul, Veda Prachayasittikul, Ratchanok Pingaew, Apilak Worachartcheewan, Supaluk Prachayasittikul, Somsak Ruchirawat Copper complexes of 8-aminoquinoline and uracils as novel aromatase inhibitors. Letters in Drug Design and Discovery. Vol.14, No.8 (2017), 880-884. doi:10.2174/1570180813666161103144822 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/41851
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Title
Copper complexes of 8-aminoquinoline and uracils as novel aromatase inhibitors
Abstract
© 2017 Bentham Science Publishers. Currently, aromatase inhibitors (AIs) have been developed for the treatment of breast cancers and other estrogen-related conditions. However, searching for more and new classes of AIs is being investigated. 8-Aminoquinoline (8AQ) is an interesting scaffold to be explored. In particular, 8AQ as its mixed ligands (5-nitrouracil, 5Nu and 5-iodouracil, 5Iu) metal complexes are potential compounds to be studied. Objective: Metal complexes of 8AQ-5Nu/5Iu were investigated for aromatase inhibitory activity and cytotoxicity. Methods: Metal complexes (1-6) and free ligands were evaluated for aromatase inhibitory and cytotoxic activities. Aromatase inhibitory activity of the metal complexes was performed according to a guideline of BD Gentest™ kit using CYP19 enzyme and O-benzyl fluorescein (DBF) as a substrate. Cytotoxic effect of the compounds was tested against normal embryonic lung cell line (MRC) using the MTT assay. Results: Significantly, copper complexes 3 (IC50 = 0.7 μM) and 6 (IC50 = 1.7 μM) were shown to be active aromatase inhibitors with selectivity indices of 24.74 and16.40, respectively. Conclusion: Copper complexes of 8AQ-5Nu (3) and of 8AQ-5Iu (6) were highlighted as novel aromatase inhibitors that could be further developed for therapeutic applications.