1982
DOI: 10.1016/s0040-4039(00)88724-9
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A novel type of bis-quinolizidine alkaloid from the sponge

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Cited by 64 publications
(27 citation statements)
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“…Sponges, in particular, are responsible for a large number of these compounds, which exhibit a wide range of activities including antitumor (Baslow and Turlapaty, 1969), antiviral (Carter and Rinehart, 1978), antibacterial (Sharma and Burkholder, 1967), and antifungal activity (Phillipson and Rinehart, 1983). The compounds also show broad chemical diversity and are among others comprised of unusual nucleosides (Quinn et al, 1980), terpenes (Cimino et al, 1971), peptides (Stonard and Andersen, 1980), alkaloids (Braekman et al, 1982), fatty acids (Morales and Litchfield, 1976), and unnatural amino acid (which are frequently halogenated) (Crews et al, 1986;Inman and Crews, 1989). It is believed that the early appearance of sponges in evolution has afforded them sufficient time to develop an advanced chemical defence system (Sipkema et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…Sponges, in particular, are responsible for a large number of these compounds, which exhibit a wide range of activities including antitumor (Baslow and Turlapaty, 1969), antiviral (Carter and Rinehart, 1978), antibacterial (Sharma and Burkholder, 1967), and antifungal activity (Phillipson and Rinehart, 1983). The compounds also show broad chemical diversity and are among others comprised of unusual nucleosides (Quinn et al, 1980), terpenes (Cimino et al, 1971), peptides (Stonard and Andersen, 1980), alkaloids (Braekman et al, 1982), fatty acids (Morales and Litchfield, 1976), and unnatural amino acid (which are frequently halogenated) (Crews et al, 1986;Inman and Crews, 1989). It is believed that the early appearance of sponges in evolution has afforded them sufficient time to develop an advanced chemical defence system (Sipkema et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…Petrosin 434 , initially extracted from marine sponge Petrosia seriata , actually is a bisquinolizidine alkaloid showing anti‐HIV activity . Total synthesis of (‐)‐ and (+)‐Petrosin 434 was accomplished and reported by Tokuyama and co‐workers in 2014.…”
Section: Coupling Of Sp3 Hybridised C–b Compoundsmentioning
confidence: 99%
“…Chemical structures of these compounds were established by comparing the NMR data ( 1 H-, 13 C-NMR, 1 H-1 H COSY, HMQC) and physical properties ([a] D , mp) with those of reported compounds. 8,9) Cells and Virus MT2 cells 10) were obtained from National AIDS Research Institute, Pune, India, and were maintained in RPMI 1640 (Sigma cat # R4130) containing 10% Fetal Bovine Serum (Sigma cat # F2442) and PenicillinStreptomycin suspension (Sigma cat # P0781) at 37°C in a 5% CO 2 humidified atmosphere incubator (Forma scientific company, U.S.A.) and splitted twice a week. Cultures were maintained in complete medium for the whole experiment.…”
Section: Animal Materialsmentioning
confidence: 99%