Marine Drugs · 2006 · 42 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyAntimicrobial ResistanceDrug DiscoveryStructure-activity RelationshipsAntibacterial AgentsAntibacterial PharmacologyAntibacterial ResistanceAntibiotic ResistanceStructure-activity Relationship AnalysisBioactive Compounds From Marine SpongesEscherichia ColiMarine AlkaloidsMarine Sponge MetabolitesPlant AlkaloidsSponges As Drug SourcesSponges-derived Metabolites
Cyclostellettamines A – F (1 – 6) isolated from the sponge Pachychalina sp. and cyclostellettamines G - I, K and L (7 – 11) obtained by synthesis were evaluated in bioassays of antimicrobial activity against susceptible and antibiotic-resistant Staphylococcus aureus, Pseudomonas aeruginosa and antibiotic-susceptible Escherichia coli and Candida albicans, as well as in antimycobacterial activity against Mycobacterium tuberculosis H37Rv bioassays. The results obtained indicated that cyclostellettamines display different antimicrobial activity depending on the alkyl-chain size, suggesting that, if a mechanism-of action is implied, it is dependent on the distance between the two pyridinium moieties of cyclostellettamines.
11
L A Collins, Scott G. Franzblau · Antimicrobial Agents and Chemotherapy · 1997 · 1.6K citations · Full text
Veterinary Medicine, Infectious Diseases, Antimicrobial Pharmacology +7
Nobuhiro Fusetani, Naoki Asai, Shigeki Matsunaga et al. · Tetrahedron Letters · 1994 · 112 citations
Marieke I.A. van der Kraan, Kamran Nazmi, Afke Teeken et al. · Biological Chemistry · 2005 · 76 citations