U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C19H36N2
Molecular Weight 292.5025
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BERTOSAMIL

SMILES

CC(C)CN1C[C@H]2CN(C[C@H](C1)[C@@]23CCCCC3)C(C)C

InChI

InChIKey=AOIVZQPSIHOHMP-ROUUACIJSA-N
InChI=1S/C19H36N2/c1-15(2)10-20-11-17-13-21(16(3)4)14-18(12-20)19(17)8-6-5-7-9-19/h15-18H,5-14H2,1-4H3/t17-,18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H36N2
Molecular Weight 292.5025
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Bertosamil was developed as an anti-ischemic and anti-arrhythmic drug that inhibits the atrial potassium channels Kv1.2, Kv1.4 and Kv1.5. However, the development of this drug has been discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanisms of action of antiarrhythmic agent bertosamil on hKv1.5 channels and outward potassium current in human atrial myocytes.
2002-02
The antiarrhythmic agent bertosamil induces inactivation of the sustained outward K+ current in human atrial myocytes.
1997-09
Inhibition by bertosamil of cardiac responses to pinacidil or Bay k 8644 in isolated dog atria and ventricles.
1996-08-01
Antiarrhythmic and bradycardic drugs inhibit currents of cloned K+ channels, KV1.2 and KV1.4.
1995-08-04
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:06:08 GMT 2025
Edited
by admin
on Wed Apr 02 09:06:08 GMT 2025
Record UNII
CB7433DY2H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BERTOSAMIL
INN  
INN  
Official Name English
bertosamil [INN]
Preferred Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
Code System Code Type Description
MESH
C103329
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
SMS_ID
100000086070
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104579
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
FDA UNII
CB7433DY2H
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID301350841
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
INN
6686
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
CAS
126825-36-3
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
PUBCHEM
16092093
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
NCI_THESAURUS
C90663
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
EVMPD
SUB05783MIG
Created by admin on Wed Apr 02 09:06:08 GMT 2025 , Edited by admin on Wed Apr 02 09:06:08 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY