| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2028520 | Steroids | 2011 | 5 Pages |
Bioassay-guided fractionation of an EtOH extract of Monascus purpureus-fermented rice led to the isolation of two new steroids (22S, 23R, 24S)-20β,23α,25α-trihydroxy-16,22-epoxy-4,6,8(14)-trienergosta-3-one (1), the first example of a steroid possessing both a conjugated triene ketone system and a fused 4H-furan ring side chain within one molecule, and (22E, 24R)-3β,5α-dihydroxyergosta-23-methyl-7,22-dien-6-one (2), as well as two known compounds (22E, 24R)-3β,5α-dihydroxyergosta-7,22-dien-6-one (3) and (22E, 24R)-6β-methoxy-ergosta-7,22-diene-3β,5α-diol (4). Their structures were assigned by detailed interpretation of HRESIMS, 1D and 2D NMR spectroscopic data. The absolute stereochemistry of 1 was determined by single-crystal X-ray crystallography while the absolute stereochemistry of 2 was established by CD. Compounds 1-4 showed cytotoxic activity against the lung adenocarcinoma (A549) with IC50 values of 0.08, 0.94, 12.6 and 13.5 μM, respectively. In addition, compounds 1 and 2 exhibited moderate activities against human ovarian cancer (A2780), with IC50 values of 2.8 and 5.1 μM.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Four steroids (compounds 1–4) were isolated from Monascus purpureus-fermented rice. ► Compound 1 represents the first example of a steroid possessing both a conjugated triene ketone system and a fused 4H-furan ring side chain within one molecule. ► The absolute configuration of 1 was determined by single-crystal X-ray. ► Compound 1 showed significant cytotoxic activity against the lung adenocarcinoma.
