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- W4206545792 endingPage "1075" @default.
- W4206545792 startingPage "1075" @default.
- W4206545792 abstract "This review comprehensively describes the recent advances in the synthesis and pharmacological evaluation of steroid polyamines squalamine, trodusquemine, ceragenins, claramine, and their diverse analogs and derivatives, with a special focus on their complete synthesis from cholic acids, as well as an antibacterial and antiviral, neuroprotective, antiangiogenic, antitumor, antiobesity and weight-loss activity, antiatherogenic, regenerative, and anxiolytic properties. Trodusquemine is the most-studied small-molecule allosteric PTP1B inhibitor. The discovery of squalamine as the first representative of a previously unknown class of natural antibiotics of animal origin stimulated extensive research of terpenoids (especially triterpenoids) comprising polyamine fragments. During the last decade, this new class of biologically active semisynthetic natural product derivatives demonstrated the possibility to form supramolecular networks, which opens up many possibilities for the use of such structures for drug delivery systems in serum or other body fluids." @default.
- W4206545792 created "2022-01-25" @default.
- W4206545792 creator A5044445427 @default.
- W4206545792 creator A5058390964 @default.
- W4206545792 creator A5067623207 @default.
- W4206545792 creator A5085097439 @default.
- W4206545792 date "2022-01-19" @default.
- W4206545792 modified "2023-10-16" @default.
- W4206545792 title "From Marine Metabolites to the Drugs of the Future: Squalamine, Trodusquemine, Their Steroid and Triterpene Analogues" @default.
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