Literature DB >> 28530828

Stachybotrysins A-G, Phenylspirodrimane Derivatives from the Fungus Stachybotrys chartarum.

Jinlian Zhao1, Jiamin Feng1, Zhen Tan1, Jimei Liu1, Jianyuan Zhao1, Ridao Chen1, Kebo Xie1, Dewu Zhang1, Yan Li1, Liyan Yu1, Xiaoguang Chen1, Jungui Dai1.   

Abstract

Seven new phenylspirodrimane derivatives named stachybotrysins A-G (2-8), together with five known compounds (1, 9-12), were isolated from Stachybotrys chartarum CGMCC 3.5365. Stachybotrysin D (5) is the first reported example of a naturally occurring alcoholic O-sulfation of a phenylspirodrimane, and stachybotrysins F and G (7 and 8) are the first examples possessing an isobenzotetrahydrofuran ring with an acetonyl moiety attached. The structures of these compounds were elucidated on the basis of extensive spectroscopic data analysis and by comparison with reported data. The absolute configurations of 1-8 were determined by X-ray single-crystal diffraction, electronic circular dichroism (ECD), and calculated ECD. Compounds 1 and 8 displayed anti-HIV activity with IC50 values of 15.6 and 18.1 μM, respectively, and 2, 7, 9, and 11 showed inhibitory effect on influenza A virus with IC50 values ranging from 12.4 to 18.9 μM.

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Year:  2017        PMID: 28530828     DOI: 10.1021/acs.jnatprod.7b00014

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  12 in total

1.  In Vitro Metabolism of Phenylspirodrimanes Derived from the Indoor Fungus Stachybotrys.

Authors:  Viktoria Lindemann; Annika Jagels; Matthias Behrens; Florian Hübner; Hans-Ulrich Humpf
Journal:  Toxins (Basel)       Date:  2022-06-08       Impact factor: 5.075

2.  Ligand-Enabled Pd(II)-Catalyzed C(sp3)-H Lactonization Using Molecular Oxygen as Oxidant.

Authors:  Shaoqun Qian; Zi-Qi Li; Minyan Li; Steven R Wisniewski; Jennifer X Qiao; Jeremy M Richter; William R Ewing; Martin D Eastgate; Jason S Chen; Jin-Quan Yu
Journal:  Org Lett       Date:  2020-04-24       Impact factor: 6.005

3.  Limonoids Containing a C₁⁻O⁻C29 Moiety: Isolation, Structural Modification, and Antiviral Activity.

Authors:  Jing-Ling Ren; Xiao-Peng Zou; Wan-Shan Li; Li Shen; Jun Wu
Journal:  Mar Drugs       Date:  2018-11-04       Impact factor: 5.118

4.  Exploring Secondary Metabolite Profiles of Stachybotrys spp. by LC-MS/MS.

Authors:  Annika Jagels; Viktoria Lindemann; Sebastian Ulrich; Christoph Gottschalk; Benedikt Cramer; Florian Hübner; Manfred Gareis; Hans-Ulrich Humpf
Journal:  Toxins (Basel)       Date:  2019-02-27       Impact factor: 4.546

Review 5.  Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes.

Authors:  Emmanuelle Lautié; Olivier Russo; Pierre Ducrot; Jean A Boutin
Journal:  Front Pharmacol       Date:  2020-04-07       Impact factor: 5.810

6.  Unconventional mechanism and selectivity of the Pd-catalyzed C-H bond lactonization in aromatic carboxylic acid.

Authors:  Li-Ping Xu; Shaoqun Qian; Zhe Zhuang; Jin-Quan Yu; Djamaladdin G Musaev
Journal:  Nat Commun       Date:  2022-01-14       Impact factor: 14.919

7.  Biosynthesis of Fungal Drimane-Type Sesquiterpene Esters.

Authors:  Ying Huang; Sandra Hoefgen; Vito Valiante
Journal:  Angew Chem Int Ed Engl       Date:  2021-10-01       Impact factor: 15.336

8.  Meroterpenoids and Isocoumarinoids from a Myrothecium Fungus Associated with Apocynum Venetum.

Authors:  Yanchao Xu; Cong Wang; Haishan Liu; Guoliang Zhu; Peng Fu; Liping Wang; Weiming Zhu
Journal:  Mar Drugs       Date:  2018-10-01       Impact factor: 5.118

9.  New Bisabosquals from Stachybotrys sp. PH30583 Elicited on Solid Media.

Authors:  Bao-Hui Ruan; Shu-Quan Li; Xue-Qiong Yang; Ya-Bin Yang; Ya-Mei Wu; Li-Jiao Shi; Hai-Yue Yin; Hao Zhou; Zhong-Tao Ding
Journal:  Molecules       Date:  2018-06-29       Impact factor: 4.411

10.  Stachybotrychromenes A-C: novel cytotoxic meroterpenoids from Stachybotrys sp.

Authors:  Annika Jagels; Yannick Hövelmann; Alexa Zielinski; Melanie Esselen; Jens Köhler; Florian Hübner; Hans-Ulrich Humpf
Journal:  Mycotoxin Res       Date:  2018-03-16       Impact factor: 3.833

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