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Compound InformationSONAR Target prediction
Name:

AMIODARONE HYDROCHLORIDE

Unique Identifier:SPE02300165
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:651.534 g/mol
X log p:15.354  (online calculus)
Lipinksi Failures2
TPSA38.77
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:4
Rotatable Bond Count:11
Canonical Smiles:Cl.CCCCc1oc2ccccc2c1C(=O)c1cc(I)c(OCCN(CC)CC)c(I)c1
Source:synthetic
Reference:Adv Drug Res 16: 309 (1987)
Therapeutics:adrenergic agonist, coronary vasodilator, Ca channel blocker
Generic_name:Amiodarone
Chemical_iupac_name:(2-butylbenzofuran-3-yl)-[4-(2-diethylaminoethoxy)-3,5-diiodo-phenyl]-methanone
Drug_type:Approved Drug
Pharmgkb_id:PA448383
Kegg_compound_id:C06823
Drugbank_id:APRD00288
H2o_solubility:50000 mg/L (chloride salt)
Logp:7.706
Cas_registry_number:1951-25-3
Drug_category:Vasodilator Agents; Enzyme Inhibitors; Anti-Arrhythmia Agents; ATC:C01BD01
Indication:Intravenously, for initiation of treatment and prophylaxis of frequently recurring
ventricular fibrillation and hemodynamically unstable ventricular tachycardia in
patients refractory to other therapy. Orally, for the treatment of life-threatening
recurrent ventricular arrhythmias such as recurrent ventricular fibrillation and
recurrent hemodynamically unstable ventricular tachycardia.
Pharmacology:Amiodarone belongs to a class of drugs called Vaughan-Williams Class III
antiarrhythmic agents. It is used in the treatment of a wide range of cardiac
tachyarhthmias, including both ventricular and supraventricular (atrial)
arrhythmias. After intravenous administration in man, amiodarone relaxes vascular
smooth muscle, reduces peripheral vascular resistance (afterload), and slightly
increases cardiac index. Amiodarone prolongs phase 3 of the cardiac action
potential. It has numerous other effects however, including actions that are similar
to those of antiarrhythmic classes Ia, II, and IV. Amiodarone shows beta
blocker-like and calcium channel blocker-like actions on the SA and AV nodes,
increases the refractory period via sodium- and potassium-channel effects, and slows
intra-cardiac conduction of the cardiac action potential, via sodium-channel
effects.
Mechanism_of_action:The 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.
Organisms_affected:Humans and other mammals

Found: 201 active | as graph: single | with analogs 2 3 4 5 6 7 8 9 10  Next >> [201]
Species: 4932
Condition: AAT2
Replicates: 2
Raw OD Value: r im 0.0992±0.0181726
Normalized OD Score: sc h 0.1347±0.0241269
Z-Score: -45.9520±0.270592
p-Value: 0
Z-Factor: 0.836126
Fitness Defect: INF
Bioactivity Statement: Active
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:5|F5
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:23.70 Celcius
Date:2008-04-08 YYYY-MM-DD
Plate CH Control (+):0.0402±0.00073
Plate DMSO Control (-):0.7159±0.01647
Plate Z-Factor:0.9139
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DBLink | Rows returned: 112 Next >> 
2156 2-[4-(2-butylbenzofuran-3-carbonyl)-2,6-diiodo-phenoxy]ethyl-diethyl-azanium
2157 (2-butylbenzofuran-3-yl)-[4-(2-diethylaminoethoxy)-3,5-diiodo-phenyl]methanone
29770 2-[4-(2-butylbenzofuran-3-carbonyl)-2,6-diiodo-phenoxy]ethyl-diethyl-azanium chloride
104774 (2-butylbenzofuran-3-yl)-[4-(2-ethylaminoethoxy)-3,5-diiodo-phenyl]methanone
178801 (2-butylbenzofuran-3-yl)-[4-(2-ethylaminoethoxy)-3,5-diiodo-phenyl]methanone hydrochloride
441325 (2-butylbenzofuran-3-yl)-[4-(2-diethylaminoethoxy)-3,5-diiodo-phenyl]methanone hydrochloride

internal high similarity DBLink | Rows returned: 2
LOPAC 00166 1.0000
RJC 02270 1.0000

active | Cluster 5540 | Additional Members: 5 | Rows returned: 2
RJC 02270 0
LOPAC 00166 0

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