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![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Three new naphthoquinone-based meroterpenoids from Streptomyces sp. HBERC-16614 with antibacterial activities
Ya-Ni Zhang1,2, Man-Li Liu1,2, Fang Liu1,2
1Hubei Biopesticide Engineering Research Centre, Hubei Academy of Agricultural Sciences, Wuhan, China.
Abstract:
Three new naphthoquinone-based meroterpenoids (1-3), including spironaphthomeroterpenoid (1), a novel naphthoquinone-based meroterpenoid with a rare [5, 6] spiro-ring skeleton, and naphthablins D and E (2-3), along with three known analogues (4-6) were isolated from Streptomyces sp. HBERC-16614. The structures of these compounds, including their absolute configurations, were established by extensive spectroscopic analysis and electronic circular dichroism (ECD) spectrum. The antibacterial activities of compounds (1-6) were evaluated against Staphylococcus aureus, Streptococcus suis, and Escherichia coli. Among them, compound 1 demonstrated potent antibacterial activity against S. aureus, with a minimum inhibitory concentration (MIC) value of 3.13 µg/mL.
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