PENG Cheng, DING Hai-e. Cyclopeptides from Fungal Endophyte Isolated from and Their Acetylcholineterase Inhibitory Activity[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(3): 32-35.
DOI:
PENG Cheng, DING Hai-e. Cyclopeptides from Fungal Endophyte Isolated from and Their Acetylcholineterase Inhibitory Activity[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(3): 32-35. DOI: 10.13422/j.cnki.syfjx.2016030032.
Cyclopeptides from Fungal Endophyte Isolated from and Their Acetylcholineterase Inhibitory Activity
have already produced many metabolites with new structures and various activities. In this paper
during the study of medicinal plant's endophytes
the author isolated and obtained Talaromyceson fungi which could produce diverse metabolites. This paper is to isolate and identify cyclopeptides from this endophytic fungus and study on their acetylcholineterase inhibitory activity. Method: The compounds were isolated by column chromatography methods
including silica gel column chromatography
punching resin column chromatography
and MCI gel chromatography;the structures of compounds were identified using wave spectrum methods
including hydrogen nuclear magnetic resonance (NMR)
carbon nuclear magnetic resonance and electrospray mass spectrometry;acetylcholineterase inhibitory activity of the compounds was detected using improved Ellman method. Result: Four cyclopeptides were isolated and identified as discarine-M(1)
fumitremorgin C(2)
fructigenine B(3)
spirotryprostatin A(4). Compound 1 showed moderate anti-acetylcholineterase activity with IC50 value of 56 μmol·L-1. Conclusion: All of the four cyclopeptides were isolated and obtained from Talaromyces genus for the first time.