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Details

Stereochemistry RACEMIC
Molecular Formula C24H27N.C6H12O7
Molecular Weight 525.6332
Optical Activity ( + / - )
Defined Stereocenters 4 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRENYLAMINE GLUCONATE

SMILES

OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.CC(CC1=CC=CC=C1)NCCC(C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=XWLQOHKWSBPMOX-IFWQJVLJSA-N
InChI=1S/C24H27N.C6H12O7/c1-20(19-21-11-5-2-6-12-21)25-18-17-24(22-13-7-3-8-14-22)23-15-9-4-10-16-23;7-1-2(8)3(9)4(10)5(11)6(12)13/h2-16,20,24-25H,17-19H2,1H3;2-5,7-11H,1H2,(H,12,13)/t;2-,3-,4+,5-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C24H27N
Molecular Weight 329.4779
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula C6H12O7
Molecular Weight 196.1553
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Prenylamine, a slow Ca2+ channel blocker, was used to treat patients with angina pectoris, but because of the QT prolongation, this drug was withdrawn from the market. Prenylamine binds to calmodulin section and inhibits myosin light chain kinase.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.72 µM [IC50]
Target ID: Q9H1R3
Gene ID: 85366.0
Gene Symbol: MYLK2
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Refining the human iPSC-cardiomyocyte arrhythmic risk assessment model.
2013-12
Comparative evaluation of HERG currents and QT intervals following challenge with suspected torsadogenic and nontorsadogenic drugs.
2006-03
[Modulation of serine/threonine protein kinase activity in chloramphenicol-resistant mutants of Streptomyces avermitilis].
2004-08-03
Female gender as a risk factor for torsades de pointes associated with cardiovascular drugs.
1993-12-01
Prevention of adriamycin-induced cardiotoxicity by prenylamine: a pilot double blind study.
1987
Atrio-ventricular block after administration of lignocaine in patients treated with prenylamine.
1982-03
An overall review on prenylamine mechanisms of action in experimental models of myocardial damage.
1982
Overdrive pacing in quinidine syncope and other long QT-interval syndromes.
1980-08
Protective effect of creatinol O-phosphate (COP) on ventricular fibrillation and death induced by intravenous CaCl2 in mice.
1979
[Prevention of isoproterenol-induced lesions in the rat myocardium by prenylamine].
1975-09-01

Sample Use Guides

270 mg of prenylamine per day for one month
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Wed Apr 02 11:38:25 GMT 2025
Edited
by admin
on Wed Apr 02 11:38:25 GMT 2025
Record UNII
Q09085O516
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRENYLAMINE GLUCONATE
Common Name English
BENZENEPROPANAMINE, N-(1-METHYL-2-PHENYLETHYL)-.GAMMA.-PHENYL-, D-GLUCONATE
Preferred Name English
PHENETHYLAMINE, N-(3,3-DIPHENYLPROPYL)-.ALPHA.-METHYL-, D-GLUCONATE
Common Name English
D-GLUCONIC ACID, COMPD. WITH N-(1-METHYL-2-PHENYLETHYL)-.GAMMA.-PHENYLBENZENEPROPANAMINE (1:1)
Systematic Name English
GLUCONIC ACID, D-, COMPD. WITH N-(3,3-DIPHENYLPROPYL)-.ALPHA.-METHYLPHENETHYLAMINE (1:1)
Systematic Name English
PRENYLAMINE D-GLUCONATE
Common Name English
Code System Code Type Description
PUBCHEM
167965
Created by admin on Wed Apr 02 11:38:25 GMT 2025 , Edited by admin on Wed Apr 02 11:38:25 GMT 2025
PRIMARY
FDA UNII
Q09085O516
Created by admin on Wed Apr 02 11:38:25 GMT 2025 , Edited by admin on Wed Apr 02 11:38:25 GMT 2025
PRIMARY
CAS
21156-48-9
Created by admin on Wed Apr 02 11:38:25 GMT 2025 , Edited by admin on Wed Apr 02 11:38:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID10943479
Created by admin on Wed Apr 02 11:38:25 GMT 2025 , Edited by admin on Wed Apr 02 11:38:25 GMT 2025
PRIMARY