Molecules · 2021 · 15 citations · 15 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsFungal Secondary MetabolitesStructure-activity Relationship AnalysisAnticancer ActivityAnticancer Compound ScreeningBacillus SubtilisChemical Structure-activity RelationshipsCircular DichroismCircular Dichroism AnalysisCytotoxicity AssaysElectronic Circular Dichroism
Seven undescribed scalarane sesterterpenoids, nambiscalaranes B–H (1–7), together with two known compounds, nambiscalarane (8) and aurisin A (9) were isolated from the cultured mycelium of the luminescent mushroom Neonothopanus nambi. Their structures were elucidated by thorough analysis of their 1D and 2D NMR spectroscopic data. The absolute configurations of 1–8 were determined by electronic circular dichroism (ECD) calculations and optical rotation measurements. The isolated sesterterpenoids were evaluated against A549, HT29, HeLa, and HCT-116 cancer cell lines, and against five bacterial strains. Compounds 3, 5, and 7 showed strong cytotoxicity against HCT-116 cell line, with IC50 values ranging from 13.41 to 16.53 µM, and showed no cytotoxicity towards Vero cells. Moreover, compound 8 inhibited the growth of Bacillus subtilis with a MIC value of 8 µg/mL, which was equivalent to the MIC value of the standard kanamycin.
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Scalarin, a new pentacyclic C-25 terpenoid from the sponge Cacospongia scalaris
Ernesto Fattorusso, Silvana Magno, C. Santacroce et al. · Tetrahedron · 1972 · 100 citations
Piyawan Kumnerdkhonkaen, Somprasong Saenglee, Md. Ali Asgar et al. · BMC Complementary and Alternative Medicine · 2018 · 48 citations · Full text
Medicine, Oncology, Pharmacology +15