JZJuan-Juan Zheng

Juan-Juan Zheng

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Juan-Juan Zheng has a total of 8 co-authors. Here are the top co-authors by number of shared publications:

  • Chang-Lun Shao

    Ocean University of China

    1 shared publication
  • Chang-Yun Wang

    Key Laboratory of Marine Drugs and Key Laboratory of Evolution and Marine Biodiversity (Ministry of Education), School of Medicine and Pharmacy, Institute of Evolution & Marine Biodiversity, Ocean University of China, Qingdao 266003, China

    1 shared publication
  • Chao-Yi Wang

    Key Laboratory of Marine Drugs, The Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China

    1 shared publication
  • Kai-Ling Wang

    Yunnan Key Laboratory of Screening and Research on Anti-Pathogenic Plant Resources from Western Yunnan, Institute of Materia Medica, College of Pharmacy, Dali University, Dali 671000, China

    1 shared publication
  • Min Chen

    Marine Science & Technology Institute, College of Environmental Science & Engineering, Yangzhou University, Yangzhou, China

    1 shared publication
  • Min Liu

    Key Laboratory of Marine Drugs, School of Medicine and Pharmacy, The Ministry of Education of China, Ocean University of China, 5 Yushan Road, Qingdao, 266003, People's Republic of China

    1 shared publication

Latest Publications

  • Open Access

    Antifouling phenyl ethers and other compounds from the invertebrates and their symbiotic fungi collected from the South China Sea

    by Chao-Yi Wang, Kai-Ling Wang, Pei-Yuan Qian, Ying Xu, Min Chen, Juan-Juan Zheng, Min Liu, Chang-Lun Shao, Chang-Yun Wang

    Marine organism-derived secondary metabolites are promising potential sources for discovering environmentally safe antifouling agents. In present study, 55 marine secondary metabolites and their synthesized derivatives were tested and evaluated for their antifouling activities and security. These compounds include 44 natural products isolated from marine invertebrates and their symbiotic microorganisms collected from the South China Sea and 11 structural modified products derived from the isolated compounds. The natural secondary metabolites, covering phenyl ether derivatives, terpenoids, 9, 11-secosteroids, anthraquinones, alkaloids, nucleoside derivatives and peptides, were isolated from two corals, one sponge and five symbiotic fungi. All of the isolated and synthesized compounds were tested for their antifouling activities against the cyprids of barnacle Balanus (Amphibalanus) amphitrite Darwin. Noticeably, five phenyl ether derivatives (9, 11, 13–15) exhibited potent anti-larval settlement activity with the EC50 values lower than 3.05 μM and the LC50/EC50 ratios higher than 15. The study of structure–activity relationship (SAR) revealed that the introduction of acetoxy groups and bromine atoms to phenyl ether derivatives could significantly improve their antifouling activities. This is the first report on the SAR of phenyl ether derivatives on antifouling activity against barnacle B. amphitrite. The polybrominated diphenyl ether derivative, 2, 4, 6, 2′, 4′, 6′-hexabromo-diorcinol (13), which displayed excellent antifouling activity, was considered as a promising candidate of environmentally friendly antifouling agents.