| Title : Acetylcholinesterase inhibitors from a marine fungus Talaromyces sp. strain LF458 - Wu_2015_Mar.Biotechnol.(NY)_17_110 |
| Author(s) : Wu B , Ohlendorf B , Oesker V , Wiese J , Malien S , Schmaljohann R , Imhoff JF |
| Ref : Mar Biotechnol (NY) , 17 :110 , 2015 |
|
Abstract :
Two new oxaphenalenone dimers, talaromycesone A (1) and talaromycesone B (2), and a new isopentenyl xanthenone, talaroxanthenone (3), together with six known diphenyl ether derivatives, e.g., Delta(1',3'),-1'-dehydroxypenicillide (4), 1',2'-dehydropenicillide (5), vermixocin A (6), vermixocin B (7), 3'-methoxy-1'2'-dehydropenicillide (8), and AS-186c (9), were isolated from the culture broth and mycelia of a marine fungus Talaromyces sp. strain LF458. Compound 2 represents the first example of 1-nor oxaphenalenone dimer carbon skeleton. All isolated compounds were subjected to bioactivity assays. Compounds 1, 2, and 9 exhibited potent antibacterial activities with IC50 3.70, 17.36, and 1.34 muM, respectively, against human pathogenic Staphylococcus strains. Compounds 1, 3, and 9 displayed potent acetylcholinesterase inhibitory activities with IC50 7.49, 1.61, and 2.60 muM, respectively. Interestingly, phosphodiesterase PDE-4B2 was inhibited by compounds 3 (IC50 7.25 muM) and 9 (IC50 2.63 muM). |
| PubMedSearch : Wu_2015_Mar.Biotechnol.(NY)_17_110 |
| PubMedID: 25108548 |
Wu B, Ohlendorf B, Oesker V, Wiese J, Malien S, Schmaljohann R, Imhoff JF (2015)
Acetylcholinesterase inhibitors from a marine fungus Talaromyces sp. strain LF458
Mar Biotechnol (NY)
17 :110
Wu B, Ohlendorf B, Oesker V, Wiese J, Malien S, Schmaljohann R, Imhoff JF (2015)
Mar Biotechnol (NY)
17 :110