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Details

Stereochemistry ACHIRAL
Molecular Formula C18H14I2O4
Molecular Weight 548.1103
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of KB-130015

SMILES

CC1=C(CC2=CC(I)=C(OCC(O)=O)C(I)=C2)C3=C(O1)C=CC=C3

InChI

InChIKey=OLIKCJUMYWSDIV-UHFFFAOYSA-N
InChI=1S/C18H14I2O4/c1-10-13(12-4-2-3-5-16(12)24-10)6-11-7-14(19)18(15(20)8-11)23-9-17(21)22/h2-5,7-8H,6,9H2,1H3,(H,21,22)

HIDE SMILES / InChI

Molecular Formula C18H14I2O4
Molecular Weight 548.1103
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Identifying regulators for EAG1 channels with a novel electrophysiology and tryptophan fluorescence based screen.
2010-09-02
The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism.
2010-04-25
The amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015) opens large-conductance Ca2+-activated K+ channels and relaxes vascular smooth muscle.
2007-01-26
Inhibition of G protein-coupled and ATP-sensitive potassium currents by 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015), an amiodarone derivative.
2004-01
Slowing of the inactivation of cardiac voltage-dependent sodium channels by the amiodarone derivative 2-methyl-3-(3,5-diiodo-4-carboxymethoxybenzyl)benzofuran (KB130015).
2003-01
Synthesis and preliminary characterization of a novel antiarrhythmic compound (KB130015) with an improved toxicity profile compared with amiodarone.
2002-01-31
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:50:11 GMT 2025
Edited
by admin
on Mon Mar 31 21:50:11 GMT 2025
Record UNII
9YA9HD8JR2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETIC ACID, 2-(2,6-DIIODO-4-((2-METHYL-3-BENZOFURANYL)METHYL)PHENOXY)-
Preferred Name English
KB-130015
Common Name English
Code System Code Type Description
PUBCHEM
9872203
Created by admin on Mon Mar 31 21:50:11 GMT 2025 , Edited by admin on Mon Mar 31 21:50:11 GMT 2025
PRIMARY
FDA UNII
9YA9HD8JR2
Created by admin on Mon Mar 31 21:50:11 GMT 2025 , Edited by admin on Mon Mar 31 21:50:11 GMT 2025
PRIMARY
CAS
147030-48-6
Created by admin on Mon Mar 31 21:50:11 GMT 2025 , Edited by admin on Mon Mar 31 21:50:11 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY