oroidin and sceptrin

oroidin has been researched along with sceptrin* in 4 studies

Other Studies

4 other study(ies) available for oroidin and sceptrin

ArticleYear
Hybrid Pyrrole-Imidazole Alkaloids from the Sponge Agelas sceptrum.
    Journal of natural products, 2016, Feb-26, Volume: 79, Issue:2

    A chemical investigation of the tropical sponge Agelas sceptrum from Plana Cays (Bahamas) led to the isolation of two hybrid pyrrole-imidazole alkaloids (PIAs), 15'-oxoadenosceptrin (1) and decarboxyagelamadin C (2). Herein, we report their challenging structure elucidation established by NMR and ECD spectroscopy. 15'-Oxoadenosceptrin (1) shows sceptrin merged with an adenine moiety, not yet encountered in the PIA family, whereas decarboxyagelamadin C (2) is a close derivative of agelamadins C to E recently isolated from an Agelas sp. from Okinawa.

    Topics: Agelas; Alkaloids; Animals; Bahamas; Hydrocarbons, Brominated; Imidazoles; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pyrroles

2016
Brominated pyrrole alkaloids from marine Agelas sponges reduce depolarization-induced cellular calcium elevation.
    Toxicon : official journal of the International Society on Toxinology, 2004, Volume: 44, Issue:1

    Seven pyrrole alkaloids isolated from Agelas sponges were tested for interactions with the cellular calcium homeostasis. Brominated pyrrole alkaloids reduced voltage dependent calcium elevation in PC12 cells. Dibromosceptrin was the most potent alkaloid with a half maximal concentration of 2.8 microM followed by sceptrin (67.5 microM) and oroidin (75.8 microM). 4,5-Dibromopyrrole-2-carboxylic acid reduced calcium elevation at concentrations exceeding 30 microM but did not eliminate calcium elevation at concentrations up to 1 mM. 4-Bromopyrrole-2-carboxylic acid and pyrrole-2-carboxylic acid were not active in this respect. The aminoimidazole group appeared to have a significant effect on voltage dependent calcium elevation shown by the comparison of oroidin with 4,5-dibromopyrrole-2-carboxylic acid. The degree of bromination of the pyrrole moiety is another important factor, as was shown by the comparison of 4,5-dibromopyrrole-2-carboxylic acid with 4-bromopyrrole-2-carboxylic acid, as well as oroidin with hymenidin and dibromosceptrin with sceptrin. The previously reported feeding deterrent activity of brominated pyrrole alkaloids in Agelas sponges against predatory reef fish may partly be explained by a general interaction of these alkaloids with the cellular calcium homeostasis. The chemoreception of bromopyrrole alkaloids in sea water is shown using sensory neurons in the rhinophore of the sea slug Aplysia punctata.

    Topics: Animals; Aplysia; Biological Transport, Active; Calcium; Calcium Channels; Carboxylic Acids; Fluorescence; Germany; Hydrocarbons, Brominated; Neurons, Afferent; PC12 Cells; Porifera; Pyrroles; Rats

2004
An analysis of phakellin and oroidin structures stimulated by further study of an Agelas sponge.
    Journal of natural products, 2004, Volume: 67, Issue:8

    Two new phakellin alkaloids, (-)-7-N-methyldibromophakellin (14) and (-)-7-N-methylmonobromophakellin (15), were isolated from an Agelas sp. sponge, collected near Wewak, Papua New Guinea. Inhibition assays employing both 12- and 15-human lipoxygenase isozymes (12-HLO, 15-HLO) were used to guide the isolation of 14, and LCMS data pointed the way to uncovering 15. The structure elucidations were completed by spectroscopic data analysis and comparisons to the properties of known phakellins. The lipoxygenase IC50 data showed that 14 was modest in its selective inhibition of 12-HLO. The phakellin family is uniquely marine-derived, and comments are offered on the biogenetic insights provided by these new structures.

    Topics: Alkaloids; Animals; Enzyme Inhibitors; Guanidines; Inhibitory Concentration 50; Lipoxygenase Inhibitors; Molecular Structure; Papua New Guinea; Piperazines; Porifera; Pyrroles; Spiro Compounds

2004
Anti-muscarinic activity of a family of C11N5 compounds isolated from Agelas sponges.
    Experientia, 1992, Sep-15, Volume: 48, Issue:9

    In a search for potential target sites for C11N5 compounds obtained from marine sponges of the genus Agelas we evaluated their interaction with muscarinic acetylcholine receptors from rat brain membranes. In competition experiments with 3H-QNB these compounds displayed the following rank order of potency: sceptrin greater than oroidin greater than or equal to dibromosceptrin greater than or equal to clathrodin. Sceptrin (50 microM) was shown to be a competitive inhibitor of 3H-QNB binding as revealed by Scatchard analysis. The results demonstrate the ability of these compounds to interact with multiple target molecules in the micromolar range.

    Topics: Alkaloids; Animals; Binding, Competitive; Brain; Cell Membrane; In Vitro Techniques; Parasympatholytics; Porifera; Pyrroles; Radioligand Assay; Rats; Receptors, Muscarinic

1992