Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.phytochem.2006.01.024
Title: Dimeric progestins from rhizomes of Ligusticum chuanxiong
Authors: Lim, L.S.
Shen, P. 
Gong, Y.H. 
Yong, E.L. 
Keywords: 3,8-Dihydro-diligustilide (1)
4,5-Dehydro-diligustilide (2)
Bioassay-guided isolation and structure elucidation
Dimeric phthalides
Levistolide A (3)
Ligusticum chuanxiong
Riligustilide (5)
Tokinolide B (4)
Umbelliferae
Issue Date: 2006
Source: Lim, L.S., Shen, P., Gong, Y.H., Yong, E.L. (2006). Dimeric progestins from rhizomes of Ligusticum chuanxiong. Phytochemistry 67 (7) : 728-734. ScholarBank@NUS Repository. https://doi.org/10.1016/j.phytochem.2006.01.024
Abstract: Five dimeric phthalides were isolated from rhizomes of Ligusticum chuanxiong and their structures deduced based on spectral data. All compounds and their parent extracts were assessed for progesterone-like activity using a progesterone receptor driven reporter-gene bioassay. Among all the compounds, riligustilide, displayed weak progesterone-like activity (EC50 ∼ 81 μM), whereas, (3Z′)-(3a′R,6′R,3R,6R,7R)-3,8-dihydro-6. 6′,7.3a′-diligustilide (Mr: 382, EC50 ∼ 90 nM), was found to be a potent and specific activator of the progesterone receptor. Levistolide A, although having a very similar plenary structure, was inactive indicating the importance of stereochemistry of chiral centers and flexibility of butylidene side chain for progestogenic activity. These bioactive phthalides and their parent extracts (EC50 ∼ 8 μg/ml) may have utility for treatment of conditions requiring progesterone action. © 2006 Elsevier Ltd. All rights reserved.
Source Title: Phytochemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/26005
ISSN: 00319422
DOI: 10.1016/j.phytochem.2006.01.024
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