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Details

Stereochemistry RACEMIC
Molecular Formula C19H33N3O
Molecular Weight 319.4848
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENTISOMIDE

SMILES

CC(C)CC(CCN(C(C)C)C(C)C)(C(N)=O)C1=CC=CC=N1

InChI

InChIKey=ZZOZYGHXNQPIPS-UHFFFAOYSA-N
InChI=1S/C19H33N3O/c1-14(2)13-19(18(20)23,17-9-7-8-11-21-17)10-12-22(15(3)4)16(5)6/h7-9,11,14-16H,10,12-13H2,1-6H3,(H2,20,23)

HIDE SMILES / InChI

Molecular Formula C19H33N3O
Molecular Weight 319.4848
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Pentisomide is an agent structurally related to disopyramide. Pentisomide is a class-I antiarrhythmic agent with a marked effect on depolarization (action of class Ia and Ic) and on repolarization. Pentisomide dose-dependently inhibited ischaemia-reperfusion arrhythmia. Pentisomide had been in phase II clinical trial for the treatment of arrhythmias. The electrophysiologic effects of pentisomide were investigated after intravenous and oral application in patients with drug refractory atrioventricular nodal tachycardia and patients with orthodromic atrioventricular re-entrant tachycardia. If intravenous pentisomide did not prevent induction of the tachycardia, oral pentisomide was not effective either. Long-term treatment with pentisomide had to be discontinued because of possible side effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Cardioprotective effects of various class I antiarrhythmic drugs in canine hearts.
1989 Jul
[Effects of oral pentisomide on ECG and hemodynamics].
1990 Dec
Effect of pentisomide (CM 7857) on myocardial excitation, conduction, repolarization, and refractoriness. An electrophysiological study in humans.
1991 Dec
Effects of pentisomide and E-4031 on canine atrial flutter due to reentry: a comparative study with disopyramide and propafenone.
1991 Jul
Evaluation of pentisomide on stable ventricular premature beats. Comparison with placebo.
1991 Jun
[Pharmacological analysis of drug interactions of disopyramide and its congeners with peripheral muscarinic acetylcholine receptors].
1991 Sep
Binding profiles of class I antiarrhythmic agents to cardiac muscarinic receptors: competitive and allosteric interactions with the receptors and their pharmacological significance.
1991 Sep
Electrophysiology and long-term efficacy of pentisomide in patients with supraventricular tachycardia.
1992 Jul
Antiarrhythmic effect related to the plasma concentration of pentisomide in vivo and the antiarrhythmic-concentration relationship in vitro.
1995

Sample Use Guides

900-1200 mg three times a day
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:25:20 GMT 2023
Edited
by admin
on Fri Dec 15 16:25:20 GMT 2023
Record UNII
506T8KTW5Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PENTISOMIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
(±)-.ALPHA.-(2-(DIISOPROPYLAMINO)ETHYL)-.ALPHA.-ISOBUTYL-2-PYRIDINEACETAMIDE
Systematic Name English
2-PYRIDINEACETAMIDE, .ALPHA.-(2-(BIS(1-METHYLETHYL)AMINO)ETHYL)-.ALPHA.-(2-METHYLPROPYL)-
Systematic Name English
PROPISOMIDE
Common Name English
ME-3202
Code English
PENTICAINIDE
Common Name English
pentisomide [INN]
Common Name English
PENTISOMIDE [MI]
Common Name English
PENTISOMIDE [MART.]
Common Name English
CM-7857
Code English
PENTISOMIDE [JAN]
Common Name English
Pentisomide [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47793
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID40869274
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
CAS
96513-83-6
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
SUPERSEDED
MERCK INDEX
m8512
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY Merck Index
SMS_ID
100000082535
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
MESH
C045930
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
FDA UNII
506T8KTW5Q
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
278-989-5
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
INN
5814
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
CAS
78833-03-1
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
PUBCHEM
65847
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
ChEMBL
CHEMBL141837
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
EVMPD
SUB09697MIG
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
NCI_THESAURUS
C90666
Created by admin on Fri Dec 15 16:25:20 GMT 2023 , Edited by admin on Fri Dec 15 16:25:20 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY