Compounds > di-n-desethylamiodarone
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di-n-desethylamiodarone and amiodarone

di-n-desethylamiodarone has been researched along with amiodarone in 4 studies

*Amiodarone: An antianginal and class III antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting POTASSIUM CHANNELS and VOLTAGE-GATED SODIUM CHANNELS. There is a resulting decrease in heart rate and in vascular resistance. [MeSH]

*Amiodarone: An antianginal and class III antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting POTASSIUM CHANNELS and VOLTAGE-GATED SODIUM CHANNELS. There is a resulting decrease in heart rate and in vascular resistance. [MeSH]

Compound Research Comparison

Studies
(di-n-desethylamiodarone)		Trials
(di-n-desethylamiodarone)		Recent Studies (post-2010)
(di-n-desethylamiodarone)		Studies
(amiodarone)		Trials
(amiodarone)		Recent Studies (post-2010) (amiodarone)
7038,1567431,889

Protein Interaction Comparison

ProteinTaxonomydi-n-desethylamiodarone (IC50)amiodarone (IC50)
Voltage-dependent L-type calcium channel subunit alpha-1CCavia porcellus (domestic guinea pig)0.27
Voltage-dependent L-type calcium channel subunit alpha-1FHomo sapiens (human)1.085
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)0.404
Bile salt export pumpHomo sapiens (human)10
Receptor tyrosine-protein kinase erbB-2Homo sapiens (human)9.148
Tyrosine-protein kinase FynHomo sapiens (human)0.817
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)2.271
Muscarinic acetylcholine receptor M2Homo sapiens (human)5.08
Muscarinic acetylcholine receptor M4Homo sapiens (human)3.63
Muscarinic acetylcholine receptor M5Homo sapiens (human)1.499
Alpha-2A adrenergic receptorHomo sapiens (human)0.312
Thyroid hormone receptor alphaHomo sapiens (human)0.65
Thyroid hormone receptor betaHomo sapiens (human)0.6
Muscarinic acetylcholine receptor M1Homo sapiens (human)2.613
Lethal factorBacillus anthracis3.5
Muscarinic acetylcholine receptor M3Homo sapiens (human)3.201
D(1A) dopamine receptorHomo sapiens (human)9.142
Sodium-dependent noradrenaline transporter Homo sapiens (human)2.271
5-hydroxytryptamine receptor 2AHomo sapiens (human)3.59
5-hydroxytryptamine receptor 2CHomo sapiens (human)0.404
Sodium-dependent serotonin transporterHomo sapiens (human)2.305
Melanocortin receptor 5Homo sapiens (human)9.497
D(3) dopamine receptorHomo sapiens (human)1.208
Sodium channel protein type 1 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 4 subunit alphaHomo sapiens (human)4.8
Squalene synthaseHomo sapiens (human)8
Delta-type opioid receptorHomo sapiens (human)8.014
5-hydroxytryptamine receptor 2BHomo sapiens (human)0.923
Sodium channel protein type 7 subunit alphaHomo sapiens (human)4.8
Voltage-dependent L-type calcium channel subunit alpha-1D Homo sapiens (human)1.085
Sodium-dependent dopamine transporter Homo sapiens (human)2.505
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)6.206
Voltage-dependent L-type calcium channel subunit alpha-1SHomo sapiens (human)1.085
Voltage-dependent L-type calcium channel subunit alpha-1CHomo sapiens (human)1.085
Sodium channel protein type 5 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 9 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 2 subunit alphaHomo sapiens (human)4.8
Sigma non-opioid intracellular receptor 1Homo sapiens (human)0.097
Sodium channel protein type 3 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 11 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 8 subunit alphaHomo sapiens (human)4.8
Sodium channel protein type 10 subunit alphaHomo sapiens (human)4.8

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bakker, O; van Beeren, HC; Wiersinga, WM1
Gilmour, BP; Lewin, AH; Navarro, HA1
Burlingame, AL; Kates, RE; Latini, R; Reginato, R1
Brecht, K; Krähenbühl, S; Lindinger, PW; Maseneni, S; Morand, R; Török, M; Zahno, A1

Other Studies

4 other study(ies) available for di-n-desethylamiodarone and amiodarone

ArticleYear
Structure-function relationship of the inhibition of the 3,5,3'-triiodothyronine binding to the alpha1- and beta1-thyroid hormone receptor by amiodarone analogs.
    Endocrinology, 1996, Volume: 137, Issue:7

    Topics: Amiodarone; Animals; Binding, Competitive; Chickens; Kinetics; Molecular Conformation; Molecular Structure; Rats; Receptors, Thyroid Hormone; Recombinant Fusion Proteins; Structure-Activity Relationship; Triiodothyronine

1996
Amiodarone and its putative metabolites fail to activate wild type hTAAR1.
    Bioorganic & medicinal chemistry letters, 2009, Oct-15, Volume: 19, Issue:20

    Topics: Amiodarone; Animals; CHO Cells; Cricetinae; Cricetulus; Humans; Rats; Receptors, G-Protein-Coupled; Transfection

2009
High-performance liquid chromatographic isolation and fast atom bombardment mass spectrometric identification of Di-N-desethylamiodarone, a new metabolite of amiodarone in the dog.
    Biomedical mass spectrometry, 1984, Volume: 11, Issue:9

    Topics: Amiodarone; Animals; Anti-Arrhythmia Agents; Benzofurans; Chemical Phenomena; Chemistry; Chromatography, High Pressure Liquid; Dogs; Humans; Mass Spectrometry; Myocardium

1984
The role of CYP3A4 in amiodarone-associated toxicity on HepG2 cells.
    Biochemical pharmacology, 2011, Feb-01, Volume: 81, Issue:3

    Topics: Amiodarone; Anti-Arrhythmia Agents; Apoptosis; Chromatography, High Pressure Liquid; Cytochrome P-450 CYP3A; Hep G2 Cells; Hepatocytes; Humans; Reactive Oxygen Species

2011