Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/99358
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Type: Journal article
Title: From sphingosine kinase to dihydroceramide desaturase: a structure-activity relationship (SAR) study of the enzyme inhibitory and anticancer activity of 4-((4-(4-chlorophenyl)thiazol-2-yl)amino)phenol (SKI-II)
Author: Aurelio, L.
Scullino, C.
Pitman, M.
Sexton, A.
Oliver, V.
Davies, L.
Rebello, R.
Furic, L.
Creek, D.
Pitson, S.
Flynn, B.
Citation: Journal of Medicinal Chemistry, 2016; 59(3):965-984
Publisher: American Chemical Society
Issue Date: 2016
ISSN: 0022-2623
1520-4804
Statement of
Responsibility: 
Luigi Aurelio, Carmen V. Scullino, Melissa R. Pitman, Anna Sexton, Victoria Oliver, Lorena Davies, Richard J. Rebello, Luc Furic, Darren J. Creek, Stuart M. Pitson and Bernard L. Flynn
Abstract: The sphingosine kinase (SK) inhibitor, SKI-II, has been employed extensively in biological investigations of the role of SK1 and SK2 in disease and has demonstrated impressive anticancer activity in vitro and in vivo. However, interpretations of results using this pharmacological agent are complicated by several factors: poor SK1/2 selectivity, additional activity as an inducer of SK1-degradation, and off-target effects, including its recently identified capacity to inhibit dihydroceramide desaturase-1 (Des1). In this study, we have delineated the structure-activity relationship (SAR) for these different targets and correlated them to that required for anticancer activity and determined that Des1 inhibition is primarily responsible for the antiproliferative effects of SKI-II and its analogues. In the course of these efforts, a series of novel SK1, SK2, and Des1 inhibitors have been generated, including compounds with significantly greater anticancer activity.
Keywords: Cell Line, Tumor
Humans
Thiazoles
Oxidoreductases
Phosphotransferases (Alcohol Group Acceptor)
Antineoplastic Agents
Enzyme Inhibitors
Drug Screening Assays, Antitumor
Cell Proliferation
Cell Survival
Molecular Structure
Structure-Activity Relationship
Dose-Response Relationship, Drug
Rights: Copyright © 2016 American Chemical Society
DOI: 10.1021/acs.jmedchem.5b01439
Grant ID: http://purl.org/au-research/grants/nhmrc/1042589
http://purl.org/au-research/grants/nhmrc/1004695
http://purl.org/au-research/grants/nhmrc/1088855
Appears in Collections:Aurora harvest 7
Molecular and Biomedical Science publications

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