The IPB has once again been recognized for its exemplary actions in terms of equal opportunity-oriented personnel and organizational policies and has received the TOTAL E-QUALITY certification for the…
The Plant Science Student Conference (PSSC) has been organised by students from the two Leibniz institutes, IPK and IPB, every year for the last 20 years. In this interview, Christina Wäsch (IPK) and…
Fobofou, S. A. T.; Franke, K.; Brandt, W.; Manzin, A.; Madeddu, S.; Serreli, G.; Sanna, G.; Wessjohann, L. A.;Bichromonol, a dimeric coumarin with anti-HIV activity from the stem bark of Hypericum roeperianumNat. Prod. Res.371947-1953(2023)DOI: 10.1080/14786419.2022.2110094
Infectious diseases caused by viruses like HIV and SARS-COV-2 (COVID-19) pose serious public health threats. In search for new antiviral small molecules from chemically underexplored Hypericum species, a previously undescribed atropisomeric C8-C8’ linked dimeric coumarin named bichromonol (1) was isolated from the stem bark of Hypericum roeperianum. The structure was elucidated by MS data and NMR spectroscopy. The absolute configuration at the biaryl axis was determined by comparing the experimental ECD spectrum with those calculated for the respective atropisomers. Bichromonol was tested in cell-based assays for cytotoxicity against MT-4 (CC50 ¼ 54 mM) cells and anti-HIV activity in infected MT-4 cells. It exhibits significant activity at EC50 ¼ 6.6–12.0 mM against HIV-1 wild type and its clinically relevant mutant strains. Especially, against the resistant variants A17 and EFVR, bichromonol is more effective than the commercial drug nevirapine and might thus have potential to serve as a new anti-HIV lead.
Publications
Agzamova, M. A.; Mamadalieva, N. Z.; Mamadalieva, N.; Porzel, A.; Hussain, H.; Dube, M.; Franke, K.; Janibekov, A.; Wessjohann, L. A.;Lehmanniaside, a new cycloartane triterpene glycoside from Astragalus lehmannianusNat. Prod. Res.37354-359(2023)DOI: 10.1080/14786419.2021.1969563
Chemical investigation of the aerial parts of Astragalus lehmannianus
Bunge (Leguminosae) led to the isolation and identification of a new
cycloartane triterpene glycoside – lehmanniaside (2\'-O-acetyl-3-β-O-D-xylopyranosyl-3β,6α,16β,24α-tetrahydroxy-20,25-epoxycycloartane).
Its structure was elucidated by means of spectroscopic analysis (HR-MS,
1D and 2D NMR). Bioassays showed that lehmanniaside exhibits weak
anthelmintic, antifungal, and cytotoxic activities.