Compounds > pyrroles
Page last updated: 2024-08-18

pyrroles and hymenidin

pyrroles has been researched along with hymenidin in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hirata, Y; Kobayashi, J; Nakamura, H; Ohizumi, Y1
Assmann, M; Köck, M; Zea, S1
Chapuis, JC; Doubek, DL; Ducki, S; Herald, DL; Pettit, GR; Schmidt, JM1
Dhawane, AN; Golen, JA; Kumbam, V; Lovely, CJ; Rasapalli, S; Rheingold, AL1
Ilaš, J; Kikelj, D; Kirby, RW; Mašič, LP; Peigneur, S; Rogers, M; Tomašič, T; Tytgat, J; Zidar, N; Žula, A1

Other Studies

5 other study(ies) available for pyrroles and hymenidin

ArticleYear
A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine sponge Hymeniacidon sp.
    Experientia, 1986, Oct-15, Volume: 42, Issue:10

    Topics: Animals; Aorta; Biological Assay; Chemical Phenomena; Chemistry; Male; Muscle Contraction; Porifera; Pyrroles; Rabbits; Receptors, Serotonin; Spectrum Analysis

1986
Sventrin, a new bromopyrrole alkaloid from the Caribbean sponge Agelas sventres.
    Journal of natural products, 2001, Volume: 64, Issue:12

    Topics: Alkaloids; Animals; Bahamas; Carboxylic Acids; Chromatography, High Pressure Liquid; Feeding Behavior; Fishes; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Porifera; Pyrroles; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared

2001
Antineoplastic agents 470. Absolute configuration of the marine sponge bromopyrrole agelastatin A.
    Oncology research, 2005, Volume: 15, Issue:1

    Topics: Alkaloids; Animals; Antineoplastic Agents; Molecular Conformation; Oxazolidinones; Porifera; Pyrroles; X-Ray Diffraction

2005
Total syntheses of oroidin, hymenidin and clathrodin.
    Organic & biomolecular chemistry, 2013, Jul-07, Volume: 11, Issue:25

    Topics: Models, Molecular; Pyrimidines; Pyrroles

2013
Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels.
    European journal of medicinal chemistry, 2017, Oct-20, Volume: 139

    Topics: Dose-Response Relationship, Drug; Humans; Molecular Structure; Potassium Channel Blockers; Potassium Channels, Voltage-Gated; Pyrroles; Structure-Activity Relationship

2017