Page last updated: 2024-09-05

ibogaine and catharanthine

ibogaine has been researched along with catharanthine in 3 studies

Compound Research Comparison

Studies
(ibogaine)
Trials
(ibogaine)
Recent Studies (post-2010)
(ibogaine)
Studies
(catharanthine)
Trials
(catharanthine)
Recent Studies (post-2010) (catharanthine)
445813684039

Protein Interaction Comparison

ProteinTaxonomyibogaine (IC50)catharanthine (IC50)
CholinesteraseHomo sapiens (human)3.17
CholinesteraseEquus caballus (horse)5.17
Transient receptor potential cation channel subfamily M member 8Mus musculus (house mouse)0.8

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arias, HR; Feuerbach, D; Jozwiak, K; Targowska-Duda, KM1
Becker, K; Brun, R; Calderón, AI; Munigunti, R1
Beatty, JW; Stephenson, CR1

Other Studies

3 other study(ies) available for ibogaine and catharanthine

ArticleYear
Catharanthine alkaloids are noncompetitive antagonists of muscle-type nicotinic acetylcholine receptors.
    Neurochemistry international, 2010, Volume: 57, Issue:2

    Topics: Animals; Calcium; Cell Line; Humans; Ibogaine; Ion Channels; Ion Transport; Muscles; Nicotinic Antagonists; Radioligand Assay; Receptors, Nicotinic; Torpedo; Tritium; Vinca Alkaloids

2010
Determination of antiplasmodial activity and binding affinity of selected natural products towards PfTrxR and PfGR.
    Natural product communications, 2013, Volume: 8, Issue:8

    Topics: Animals; Antiprotozoal Agents; Biological Products; Glutathione Reductase; Humans; Ibogaine; Indole Alkaloids; Inhibitory Concentration 50; Plasmodium falciparum; Thioredoxin-Disulfide Reductase; Vinca Alkaloids

2013
Synthesis of (-)-pseudotabersonine, (-)-pseudovincadifformine, and (+)-coronaridine enabled by photoredox catalysis in flow.
    Journal of the American Chemical Society, 2014, Jul-23, Volume: 136, Issue:29

    Topics: Catalysis; Ibogaine; Indole Alkaloids; Light; Molecular Conformation; Oxidation-Reduction; Photochemical Processes; Stereoisomerism; Vinca Alkaloids

2014