Journal of Asian Natural Products Research · 2017 · 12 citations · 11 references
Life SciencesBiochemistryBotanyBioorganic ChemistryDrug DiscoveryStructure-activity RelationshipsAromatic PlantsMedicinal PlantsStructure-activity Relationship AnalysisActive Compound IsolationAntimicrobial MetabolitesBacillus SubtilisBioactive Plant CompoundsBotanical BioassaysPhytochemical CompositionThree-dimensional Nmr SpectroscopyTwo-dimensional Nmr Spectroscopy
A phytochemical study on the whole plant of Spermacoce latifolia led to the isolation of a new anthraquinone, 1,2,6-trihydroxy-5-methoxy-9,10-anthraquinone (1), and a new naphthoquinone, (2R)-6-hydroxy-7-methoxy-dehydroiso-α-lapachone (2), together with three known anthraquinones (3–5). Their structures were established on the basis of detailed spectroscopic analysis, including one- and two-dimensional NMR, ESI–MS, and HR–ESI–MS techniques. All the compounds were isolated from S. latifolia for the first time. Compounds 1, 2, 4, and 5 showed significant antibacterial activity toward Bacillus subtilis with MIC values ranging from 0.9 to 31.2 μg/ml, and compound 4 aslo exhibited antibacterial activity against Bacillus cereus with a MIC value 62.5 μg/ml. Compound 1 was further revealed to show significant in vitro α-glucosidase inhibitory activity with IC50 value of 0.653 mM.
11
Antifungal and antibacterial naphthoquinones from Newbouldia laevis roots
Stefan Gafner, Jean‐Luc Wolfender, Malo Nianga et al. · Phytochemistry · 1996 · 133 citations
Antiosteoporotic Activity of Anthraquinones from Morinda officinalis on Osteoblasts and Osteoclasts
Yanbin Wu, Chengjian Zheng, Luping Qin et al. · Molecules · 2009 · 126 citations · Full text
Bioactive Furanonaphthoquinones from Crescentia cujete
Carl E. Heltzel, A. A. Leslie Gunatilaka, Thomas E. Glass et al. · Journal of Natural Products · 1993 · 57 citations