Publications by authors named "Mengting Teng"

A 3,4-dihydroisocoumarin derivative fused with dihydrothiophene, talarolactone A (), and two known compounds, terreusinone () and 4,6-dihydroxy-5-methylphthalide (), were isolated from sp. associated with . The structure of was deduced from extensive spectroscopic data, electronic circular dichroism calculations, and X-ray diffraction analyses.

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Infections caused by bacteria represent an emerging public health threat due to the development of antibiotic resistance in bacteria. Curcumin (CUR), a naturally derived substance, is found to be effective against several bacteria. However, its use is limited by its low water solubility and rapid degradation profile.

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Background: The potassium dichromate oxidation method used in determination of alcohols in fermentation has two major disadvantages. This method cannot be used to determine alcohols in raw fermentation broth samples, which often contain various reducing sugars. The method is not environment friendly due to the carcinogenicity of Cr (VI) used.

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Article Synopsis
  • Six tetranuclear metallacycles and three hexanuclear metallacages were created through coordinated self-assembly involving imidazole-based compounds and various dinuclear ruthenium(II) acceptors.
  • The self-assembly process led to the formation of stable and symmetrical structures, despite potential for isomeric variations due to different binding interactions.
  • The resulting complexes, particularly those with the 5,8-dioxido-1,4-naphtoquinonato spacer, demonstrated promising anticancer effects while showing lower toxicity to normal cells, and strong binding to ctDNA was highlighted as a key feature of one specific complex.
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The active metabolites investigation of Talaromyces sp. (strain No. MH551540) associated with Xanthoparmelia angustiphylla afforded one new δ-lactone, talaromycin A (1), together with six known compounds, clearanol A (2), 6-methylbiphenyl-3,3',4,5'-tetraol (3), desmethylaltenusin (4), ergone (5), ergosterol (6), and palmitic acid (7).

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