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Two new bisabolane-type sesquiterpenoids, aspergillolanoids A and B (1 and 2), along with a previously unreported cyclic tetrapeptide, aspergitertide A (5), and four known compounds (3, 4, 6 and 7), have been isolated from the deep-sea-derived fungus Aspergillus sp. WHUF05242. Structural elucidation of these compounds was accomplished through comprehensive spectroscopic analysis, including HR-ESIMS and 1D/2D NMR spectroscopic data. The absolute stereochemistry of 1 was unambiguously determined by single-crystal X-ray crystallographic analysis, while the chiral center configurations of 5 were resolved through time-dependent density functional theory (TDDFT)-based ECD calculations. Antimicrobial evaluation revealed that compound 7 demonstrated moderate antibacterial activity against Staphylococcus aureus with MIC value of 16 μg/mL.
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http://dx.doi.org/10.1016/j.fitote.2025.106547 | DOI Listing |
Phytochemistry
November 2025
State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization and the Key Laboratory of Plant Resources and Chemistry of Arid Zone, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China; College of Pharmacy, Xinjiang Medic
Eleven previously undescribed bisabolane-type sesquiterpenoids were successfully isolated from Artemisia persica. The structures of these compounds were comprehensively elucidated through a combination of advanced spectroscopic techniques, including one-dimensional and two-dimensional nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, and ultraviolet spectroscopy. Structural assignments were further confirmed by comparison of experimental and time-dependent density functional theory-calculated electronic circular dichroism spectra, as well as single-crystal X-ray diffraction analysis where applicable.
View Article and Find Full Text PDFFitoterapia
June 2025
Department of Pharmacy, Renmin Hospital of Wuhan University, Wuhan 430060, China; Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education and School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China. Electronic address:
Two new bisabolane-type sesquiterpenoids, aspergillolanoids A and B (1 and 2), along with a previously unreported cyclic tetrapeptide, aspergitertide A (5), and four known compounds (3, 4, 6 and 7), have been isolated from the deep-sea-derived fungus Aspergillus sp. WHUF05242. Structural elucidation of these compounds was accomplished through comprehensive spectroscopic analysis, including HR-ESIMS and 1D/2D NMR spectroscopic data.
View Article and Find Full Text PDFChem Biodivers
August 2025
School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Sanguisorba officinalis L. (Di-Yu in Chinese) is a traditional herbal plant that belongs to the genus Sanguisorba (Rosaceae). Four new bisabolane-type sesquiterpenoids (1-4) and two known monoterpenoids (5 and 6) were isolated from the roots of S.
View Article and Find Full Text PDFFitoterapia
March 2025
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China; School of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China. Electronic address:
Five new bisabolane-type sesquiterpenoids (1-5) were isolated from the rhizomes of Curcuma longa, and all of them were oxygen-containing heterocyclic compounds. The structures of the compounds were elucidated using comprehensive spectroscopic techniques, and their absolute configurations were confirmed through electronic circular dichroism (ECD) calculations. All of the compounds were evaluated for their vasorelaxant and anti-inflammatory activities.
View Article and Find Full Text PDFChin J Nat Med
November 2024
Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China. Electronic address:
A phytochemical investigation of the whole plant of Parasenecio rubescens (S. Moore) Y. L.
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