Abstract |
PF-543, the most potent sphingosine kinase (SK) inhibitor, does not demonstrate effective anticancer activity in some cancer cells, unlike other known SK1 inhibitors. PF-543 has a non- lipid structure with a unique toluene backbone; however, the importance of this structure remains unclear. Therefore, the purpose of this study was to investigate changes in SK inhibitory and anticancer activities and to explore the role of the tolyl group structure of PF-543 through various modifications. We transformed the methyl group of PF-543 into hydrogen, fluorine, and hydroxy. PF-543 derivatives in which the methyl group was substituted by hydrogen and fluorine (compound 5) demonstrated SK1 inhibitory and anticancer activities similar to PF-543. Moreover, we performed molecular modeling studies of PF-543 and compound 5. To assess the metabolic stability of PF-543 and compound 5, we determined their degree of degradation using the liver microsomes of four different animal species (human, dog, rat, and mouse). However, both PF-543 and compound 5 showed poor microsomal stability. Therefore, for the medical applications of PF-543, the structural modifications of its other parts may be necessary. Our results provide important information for the design of additional PF-543 analogs.
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Authors | Su Bin Kim, Taeho Lee, Hong Seop Moon, Sung Hwan Ki, Yoon Sin Oh, Joo-Youn Lee, Sang-Bum Kim, Jeong-Eun Park, Yongseok Kwon, Sanghee Kim, Dong Jae Baek, Eun-Young Park |
Journal | Molecules (Basel, Switzerland)
(Molecules)
Vol. 25
Issue 11
(May 27 2020)
ISSN: 1420-3049 [Electronic] Switzerland |
PMID | 32471162
(Publication Type: Journal Article)
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Chemical References |
- 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
- Boron Compounds
- PF-543
- Pyrrolidines
- Sulfones
- Phosphotransferases (Alcohol Group Acceptor)
- sphingosine kinase
- Methanol
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Topics |
- Animals
- Boron Compounds
- Dogs
- Humans
- Methanol
(chemistry, pharmacology)
- Mice
- Microsomes, Liver
(drug effects, metabolism)
- Phosphotransferases (Alcohol Group Acceptor)
(antagonists & inhibitors, metabolism)
- Pyrrolidines
(chemistry, pharmacology)
- Rats
- Structure-Activity Relationship
- Sulfones
(chemistry, pharmacology)
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