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HCID 2157Erstellt: 25. Oktober 2026

Amiodaron

Amiodarone Base · Ancaron · Atlansil · Sedacoron · AMidorone · Sedacorone · Amiodarons · amiodarona

https://huagongshe.com/de/chemical/2157

Molekülstruktur von Amiodaron

Identifikatoren & physikalische Daten

CAS No.1951-25-3
SummenformelC25H29I2NO3
Durchschnittliche Molmasse645,3 g/mol
Monoisotopische Masse645,02368979 g/mol
SMILESCCCCc1oc2ccccc2c1C(=O)c1cc(I)c(OCCN(CC)CC)c(I)c1
InChIKeyIYIKLHRQXLHMJQ-UHFFFAOYSA-N
PubChem CID2157
ChEMBLCHEMBL633
ChEBICHEBI:2663
EC No.217-772-1
DTXSIDDTXSID7022592
Lokaler NameAmiodaron

Chemische & physikalische Eigenschaften

XLogP7,6
Polarare Oberfläche (TPSA)42,7
H-Brücken-Donoren0
H-Brücken-Akzeptoren4
Frei drehbare Bindungen11
Schwere Atome31
Formalladung0
Komplexität547
ArzneimittelPharmaceuticals -> Listed in ZINC15Pharmaceuticals -> Used in Switzerland
LogP (Verteilungskoeffizient)7.96.59
LöslichkeitLow4.76e-03 g/LChloroform (Slightly), Methanol (Slightly)716.4mg/L(25 ºC)
Human DrugsBreast FeedingLactationMilk, HumanAntiarrhythmicsPharmaceuticalsAntiarrhythmic medicines
Endocrine DisruptorsPotential endocrine disrupting compound
Physical DescriptionSolid
Ionization EfficiencyPositive4.7016910252.7Thermo LTQElectrospray ionizationformic acid (5.3nM)
Dissociation Constants9.066.56 ± 0.06
Collision Cross Section223.8 Ų [M+H]+ [CCS Type: DTBuffer gas: N2Ionization: APCI+Dataset: TOXCASTSource Identifier: DTXSID7037185]224.84 Ų [M+H]+ [CCS Type: TWMethod: calibrated with polyalanine and drug standards]226.4 Ų [M+H]+ [CCS Type: TWMethod: Major Mix IMS/Tof Calibration Kit (Waters)]
Schmelzpunkt54 - 55°C
Siedepunkt635.1±55.0 °C(Predicted)
Dichte1.5730 (estimate)
Lagerbedingungen2-8°C
AggregatzustandSolid
pKa (Säurekonstante)6.56(at 25℃)
FarbeColourless to Pale Yellow
StabilitätStable. Incompatible with strong oxidizing agents.
InChIInChI=1S/C25H29I2NO3/c1-4-7-11-22-23(18-10-8-9-12-21(18)31-22)24(29)17-15-19(26)25(20(27)16-17)30-14-13-28(5-2)6-3/h8-10,12,15-16H,4-7,11,13-14H2,1-3H3
InChIKeyIYIKLHRQXLHMJQ-UHFFFAOYSA-N
SMILESC(C1C2=CC=CC=C2OC=1CCCC)(C1=CC(I)=C(OCCN(CC)CC)C(I)=C1)=O
CAS Datenbank1951-25-3(CAS DataBase Reference)
EPA chemische InformationenMethanone, (2-butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl]- (1951-25-3)

Sicherheit & Vorschriften

GHS-EinstufungThis chemical does not meet GHS hazard criteria for 96.4% (53 of 55) of all reports.Not ClassifiedAggregated GHS information provided per 55 reports by companies from 3 notifications to the ECHA C&L Inventory.
Regulatorische InformationenAmiodarone: Does not have an individual approval but may be used under an appropriate group standard
Weitere SicherheitsinformationenIMAP assessments - Methanone, (2-butyl-3-benzofuranyl)[4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl]-: Human health tier I assessment
Hazard Classes and CategoriesNot Classified
Gesundheitliche AuswirkungenSome side effects have a significant mortality rate: specifically, hepatitis, exacerbation of asthma and congestive failure, and pneumonitis.
HepatotoxicityWhile liver injury from amiodarone is uncommon, it is not rare. Serum enzyme elevations are reported to occur in 15% to 50% of patients on long term therapy, but with lower doses (200 to 300 mg daily), ALT elevations are less common. Often these elevations resolve despite continuation of amiodarone, and liver biopsy may reveal minimal changes, or accumulation of granular material in macrophages without other evidence of injury. Patients taking amiodarone are recommended to have ALT and AST values taken at baseline and then every six months, and to discontinue therapy if levels are persistently greater than twice the upper limit of the normal range. The efficacy of this approach, even if followed, in preventing serious liver injury from amiodarone is unclear.
Unerwünschte WirkungenAdverse effects from amiodarone therapy can be as high as 15% within the initial year of use and may reach 50% with long-term treatment. The risk-to-benefit ratio frequently results in the discontinuation of amiodarone within the first year of treatment, particularly for patients with atrial fibrillation. The most prevalent adverse effect is the development of corneal microdeposits, which occur in at least 90% of patients taking amiodarone. This occurrence is believed to result from amiodarone being secreted in the lacrimal gland and subsequently taken up by the corneal epithelium. However, only about 10% of these patients will develop actual visual symptoms. Additional ocular adverse effects include photophobia, optic neuropathy, and visual halos. A baseline ophthalmological assessment is recommended for patients initiating amiodarone therapy.
ExpositionspfadeSlow and variable (about 20 to 55% of an oral dose is absorbed).
ToxizitätsübersichtSigns and Symptoms of OverdoseThe antiarrhythmic effect of amiodarone may be due to at least two major actions. It prolongs the myocardial cell-action potential (phase 3) duration and refractory period and acts as a noncompetitive a- and b-adrenergic inhibitor.
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).
Drug Induced Liver InjuryBenchmark Dataset for the Liver Toxicity Knowledge Base (LTKB)amiodaroneCordarone®Antiarrhythmics8most-DILI-concern
Effects During Pregnancy and Lactation◉ Summary of Use during Lactation
Toxicity DataIntravenous, mouse: LD<sub>50</sub> = 178 mg/kg.
EPA Human Health Benchmarks for PharmaceuticalsAmiodarone9.339.4When adequate arrhythmia control is achieved, or if side effects become prominent, amiodarone dose should be reduced to 600 to 800 mg/day for one month and then to the maintenance dose, usually 400 mg/day.Data used to generate the benchmarks include the following: Lowest Daily Dose (LDD): 400 mg/day, Lowest Therapeutic Dose (LTD): 5.0 mg/kg-day, and Screening Dose: 0.002 mg/kg-day.15-Dec-21
Wassergefährdungsklasse (WGK)3
RTECS-Nr.OB1361000
R-Sätze (R)20/21/22
GefahrensymboleXn
Sicherheitshinweise (S)36

Anwendungen & Verwendung

Beschreibung

From the chemical point of view, amiodarone is completely different from other antiarrhythmics. It has two iodide atoms and a diethylaminoethanol group as substituents in the benzoyl part, and overall it is very similar to the structure of thyroxin-like molecules.

Verwenden

antibacterial