Published May 31, 2019 | Version v1
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Fig. 6 in 4-Hydroxybenzoic acid serves as an endogenous ring precursor for antroquinonol biosynthesis in Antrodia cinnamomea

  • 1. ∗∗ & Department of Horticulture and Landscape Architecture, National Taiwan University, Taipei, Taiwan, ROC & Joint Center for Instruments and Researches, College of Bioresources and Agriculture, National Taiwan University, Taipei, Taiwan, ROC

Description

Fig. 6. Proposed precursor-product relationships diagram of AQ and 4-AAQB in A. cinnamomea. The formation of the farnesyl tails of AQ and 4-AAQB are formed via mevalonate pathway. The benzoquinone ring of AQ can be formed via both shikimate pathway and polyketide pathway, but that of 4-AAQB and its intermediates synthesized only via polyketide pathway. The ring formed via polyketide pathway is marked in red color, and that formed via shikimate pathway is marked in blue color.

Notes

Published as part of Chou, Kevin Chi-Chung, Wu, Hsiang-Lin, Lin, Pei-Yin, Yang, Shang-Han, Chang, Tsu-Liang, Sheu, Fuu, Chen, Kai-Hsien & Chiang, Been-Huang, 2019, 4-Hydroxybenzoic acid serves as an endogenous ring precursor for antroquinonol biosynthesis in Antrodia cinnamomea, pp. 97-106 in Phytochemistry 161 on page 104, DOI: 10.1016/j.phytochem.2019.02.011, http://zenodo.org/record/10481992

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Journal article: 10.1016/j.phytochem.2019.02.011 (DOI)
Journal article: urn:lsid:plazi.org:pub:F0154E7BFF93FFFFFF9FFF8CFFA2B010 (LSID)
Journal article: https://zenodo.org/record/10481992 (URL)