ChemSpider 2D Image | Amiodarone HCl | C25H30ClI2NO3

Amiodarone HCl

  • Molecular FormulaC25H30ClI2NO3
  • Average mass681.773 Da
  • Monoisotopic mass681.000366 Da
  • ChemSpider ID27664

More details:

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(2-butyl-1-benzofur-3-yl){4-[2-(diéthylamino)éthoxy]-3,5-diiodophényl}méthanone chlorhydrate
(2-Butyl-1-benzofur-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodphenyl}methanonhydrochlorid
(2-Butyl-1-benzofuran-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl}methanone hydrochloride
(2-Butyl-1-benzofuran-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl}methanone hydrochloride (1:1) [ACD/IUPAC Name]
(2-Butyl-1-benzofuran-3-yl){4-[2-(diéthylamino)éthoxy]-3,5-diiodophényl}méthanone, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
(2-Butyl-1-benzofuran-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodphenyl}methanonhydrochlorid (1:1) [German] [ACD/IUPAC Name]
(2-butylbenzo[b]furan-3-yl){4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl}methanone hydrochloride
19774-82-4 [RN]
200-659-6 [EINECS]
243-293-2 [EINECS]
More...

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

976728SY6Z [DBID]
UNII-976728SY6Z [DBID]
1951-25-3,9774-82-4 [DBID]
A8423_SIGMA [DBID]
D00636 [DBID]
EU-0100122 [DBID]
HSDB 6525 [DBID]
L-3428 [DBID]
MLS000028520 [DBID]
NSC 85442 [DBID]
More...
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Target Organs:

      Potassium Channel; Adrenergic Receptor antagonist TargetMol T1496

    • Bio Activity:

      Amiodarone is an antiarrhythmic drug for inhibition of ATP-sensitive potassium channel with IC50 of 19.1 ?M. MedChem Express HY-14188
      Broad spectrum ion channel blocker; antiarrhythmic Tocris Bioscience 4095
      Broad-spectrum ion channel blocker; blocks late INa, ICa, IKr and IKs and increases QT. Displays class III antiarrhythmic properties. Also exhibits fungicidal activity; elicits Ca2+ influx in Saccharo myces cerevisiae and causes mitochondrial fragmentation and cell death. Thought to stimulate autophagy by targeting upstream mTORC1 control pathways. Selectively toxic to NSCs in hESC-derived cell pop ulations. Tocris Bioscience 4095
      Broad-spectrum ion channel blocker; blocks late INa, ICa, IKr and IKs and increases QT. Displays class III antiarrhythmic properties. Also exhibits fungicidal activity; elicits Ca2+ influx in Saccharomyces cerevisiae and causes mitochondrial fragmentation and cell death. Thought to stimulate autophagy by targeting upstream mTORC1 control pathways. Selectively toxic to NSCs in hESC-derived cell populations. Tocris Bioscience 4095
      Ion Channels Tocris Bioscience 4095
      Membrane Tranporter/Ion Channel MedChem Express HY-14188
      Membrane Tranporter/Ion Channel; MedChem Express HY-14188
      Membrane Transporter/Ion Channel; GPCR/G Protein TargetMol T1496
      Other Channel Modulators Tocris Bioscience 4095
      Potassium Channel MedChem Express HY-14188
      Potassium Channel ;??-adrenergic receptor TargetMol T1496

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


Advertisement