Responsive image

Common name


Encainide

IUPAC name


4-methoxy-N-{2-[2-(1-methylpiperidin-2-yl)ethyl]phenyl}benzamide

SMILES


COC1=CC=C(C=C1)C(=O)NC1=CC=CC=C1CCC1CCCCN1C

Compound class


Anti-Arrhythmia Agents; Voltage-Gated Sodium Channel Blockers; Sodium Channel Blockers; Cardiovascular System; Antiarrhythmics, Class I and Iii; Cardiac Therapy; Antiarrythmics, Class I and Iii; Antiarrhythmics, Class Ic; CYP2D6 Inducers; CYP2D6 Inducers (strong);

Therapeutic area


Encainide is a class Ic antiarrhythmic agent which was used for management of irregular heartbeats, such as atrial fibrillation, atrial flutter, ventricular tachycardia, and ventricular fibrillation.

Common name


Encainide

IUPAC name


4-methoxy-N-{2-[2-(1-methylpiperidin-2-yl)ethyl]phenyl}benzamide

SMILES


COC1=CC=C(C=C1)C(=O)NC1=CC=CC=C1CCC1CCCCN1C

INCHI


InChI=1S/C22H28N2O2/c1-24-16-6-5-8-19(24)13-10-17-7-3-4-9-21(17)23-22(25)18-11-14-20(26-2)15-12-18/h3-4,7,9,11-12,14-15,19H,5-6,8,10,13,16H2,1-2H3,(H,23,25)

FORMULA


C22H28N2O2

Responsive image

Common name


Encainide

IUPAC name


4-methoxy-N-{2-[2-(1-methylpiperidin-2-yl)ethyl]phenyl}benzamide

Molecular weight


352.470

clogP


4.095

clogS


-5.481

HBond Acceptor


3

HBond Donor


1

Total Polar
Surface Area


41.57

Number of Rings


3

Rotatable Bond


6

Drug ID Common name Structure CAS SMILE Frequency
FDBF00003 formamide Responsive image C(=O)N 0.1240
FDBF00005 benzene Responsive image c1ccccc1 0.2824
FDBF00048 benzamide Responsive image O=C(N)c1ccccc1 0.0117
FDBF00141 ethylbenzene Responsive image c1(ccccc1)CC 0.0371
FDBF01529 4-methoxybenzamide Responsive image O=C(N)c1ccc(cc1)OC 0.0014
FDBF01583 (2R)-1,2-dimethylpiperidine Responsive image N1(C(CCCC1)C)C 0.0010
FDBF01584 (2R)-2-ethyl-1-methyl-piperidine Responsive image N1(C(CCCC1)CC)C 0.0010
FDBF01731 N-(o-tolyl)formamide Responsive image O=CNc1c(cccc1)C 0.0034
FDBF01952 N-phenylbenzamide Responsive image c1(ccccc1)C(=O)Nc2ccccc2 0.0010
FDBF02772 4-methoxy-N-phenyl-benzamide Responsive image c1(ccc(cc1)OC)C(=O)Nc2ccccc2 0.0003
13 , 2