Literature

Abstract

Two indole-alkaloid isoprenoids were isolated from extracts of Penicillium crustosum Thom grown on rice. Their structures were elucidated on the basis of various NMR experiments and by comparison to the structurally related penitrems. The two compounds, designated thomitrem A and thomitrem E, contain a 18(19)-double bond and lack the characteristic penitrem 17(18)-ether linkage. (C) 2002 Elsevier Science Ltd. All rights reserved.

DOI： 10.1016/S0031-9422(02)00369-2

Thomitrems A and E, two indole-alkaloid isoprenoids from Penicillium crustosum Thom

Phytochemistry 2002.0

Studies on fungal products. Part XXXIII. Structures of new indoloditerpenes, possible biosynthetic precursors of the tremorgenic mycotoxins, penitrems, from Penicillium crustosum.

Chemical and Pharmaceutical Bulletin 1990.0

Pennigritrem, a naturally-occurring penitrem A analogue with novel cyclisation in the diterpenoid moiety

Journal of the Chemical Society, Perkin Transactions 1 1992.0

Two new indole-diterpenoids from the fungusPenicilliumcrustosumYN-HT-15

Journal of Asian Natural Products Research 2014.0

Janthitrems B and C, two principal indole-diterpenoids produced by Penicillium janthinellum

Phytochemistry 1993.0

Tremorgenic mycotoxins from Penicillium crustosum: isolation of penitrems A–F and the structure elucidation and absolute configuration of penitrem A