Reinvestigation of Mycothiazole Reveals the Penta-2,4-dien-1-ol Residue Imparts Picomolar Potency and 8 S Configuration

Reinvestigation of mycothiazole ( ) revealed picomolar potency (IC = 0.00016, 0.00027, 0.00035 μM) against pancreatic, (PANC-1), liver (HepG2), and colon (HCT-116) tumor cell lines. Reevaluation of provided [α] data indicating Vanuatu specimens of contain the 8 enantiomer of and not the 8 configurat...

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Veröffentlicht in:ACS medicinal chemistry letters 2020-02, Vol.11 (2), p.108-113
Hauptverfasser: Johnson, Tyler A, Morris, Joseph D, Coppage, David A, Cook, Colon V, Persi, Lauren N, Ogarrio, Marcos A, Garcia, Taylor C, McIntosh, Nicole L, McCauley, Erin P, Media, Joseph, Maheshwari, Mani, Valeriote, Frederick A, Shaw, Jiajiu, Crews, Phillip
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Sprache:eng
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Zusammenfassung:Reinvestigation of mycothiazole ( ) revealed picomolar potency (IC = 0.00016, 0.00027, 0.00035 μM) against pancreatic, (PANC-1), liver (HepG2), and colon (HCT-116) tumor cell lines. Reevaluation of provided [α] data indicating Vanuatu specimens of contain the 8 enantiomer of and not the 8 configuration previously reported. Semisynthesis provided 8- -acetylmycothiazole ( ), 8-oxomycothiazole ( ), mycothiazole nitrosobenzene derivatives (MND1, MND2: , ), and MND3 ( ) with IC = 0.00129, >1.0, >1.0, >1.0, >1.0 μM, respectively, against PANC-1 cell lines. These results highlight the significance of the penta-2,4-dien-1-ol residue as a key structural feature of required for its cytotoxicty against tumor cell lines.
ISSN:1948-5875
1948-5875
DOI:10.1021/acsmedchemlett.9b00302