DRONEDARONE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C31H44N2O5S
Molecular Weight	556.756
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of DRONEDARONE

Structure Search

SMILES

CCCCN(CCCC)CCCOC1=CC=C(C=C1)C(=O)C2=C(CCCC)OC3=CC=C(NS(C)(=O)=O)C=C23

InChI

InChIKey=ZQTNQVWKHCQYLQ-UHFFFAOYSA-N

InChI=1S/C31H44N2O5S/c1-5-8-12-29-30(27-23-25(32-39(4,35)36)15-18-28(27)38-29)31(34)24-13-16-26(17-14-24)37-22-11-21-33(19-9-6-2)20-10-7-3/h13-18,23,32H,5-12,19-22H2,1-4H3

HIDE SMILES / InChI

Approval Year

Name

Type

Language

DRONEDARONE

Official Name

English

dronedarone [INN]

Common Name

English

METHANESULFONAMIDE, N-(2-BUTYL-3-(4-(3-(DIBUTYLAMINO)PROPOXY)BENZOYL)-5-BENZOFURANYL)-

Systematic Name

English

SR33589

Code

English

SR-33589

Code

English

DRONEDARONE [VANDF]

Common Name

English

N-(2-BUTYL-3-(4-(3-(DIBUTYLAMINO)PROPROXY)BENZOYL)BENZOFURAN-5-YL)METHANESULFONAMIDE

Common Name

English

DRONEDARONE [EMA EPAR]

Common Name

English

Dronedarone [WHO-DD]

Common Name

English

DRONEDARONE [MI]

Common Name

English

DRONEDARONE [MART.]

Common Name

English

Classification Tree Code System Code

WHO-VATC

QC01BD07

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

LIVERTOX

NBK548208

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

NDF-RT

N0000175426

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

WHO-ATC

C01BD07

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

NCI_THESAURUS

C47793

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

Code System Code Type Description

WIKIPEDIA

DRONEDARONE

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

DRUG BANK

DB04855

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

NDF-RT

N0000185503

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

P-Glycoprotein Inhibitors [MoA]

RXCUI

233698

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

RxNorm

SMS_ID

100000081006

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

PUBCHEM

208898

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

MESH

C118667

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

EPA CompTox

DTXSID3048653

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

HSDB

7928

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

MERCK INDEX

m4768

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

Merck Index

NDF-RT

N0000182137

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

Cytochrome P450 2D6 Inhibitors [MoA]

IUPHAR

7465

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

CAS

141626-36-0

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

EVMPD

SUB06408MIG

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

DAILYMED

JQZ1L091Y2

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

ChEMBL

CHEMBL184412

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

NDF-RT

N0000190114

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

Cytochrome P450 3A Inhibitors [MoA]

CHEBI

50659

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

NCI_THESAURUS

C65485

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

INN

7382

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

FDA UNII

JQZ1L091Y2

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

DRUG CENTRAL

4112

Created by admin on Fri Dec 15 16:18:50 UTC 2023 , Edited by admin on Fri Dec 15 16:18:50 UTC 2023

PRIMARY

ACTIVE MOIETY


					JQZ1L091Y2

METABOLITE (PARENT)


					N9M9R8L6HY

N-(2-BUTYL-3-(4-(3-HYDROXYPROPOXY)BENZOYL)-5-BENZOFURANYL)METHANESULFONAMIDE

METABOLITE (PARENT)


					P7K8A6HQU5

3-(4-((2-BUTYL-5-((METHYLSULFONYL)AMINO)-3-BENZOFURANYL)CARBONYL)PHENOXY)PROPANOIC ACID

METABOLITE (PARENT)


					V4SVV994JM

N-(2-BUTYL-3-(4-(3-(2-HYDROXYETHYLAMINO)PROPOXY)BENZOYL)BENZOFURAN-5-YL)METHANESULFONAMIDE

METABOLITE (PARENT)


					HJS89VA2WC

(5-AMINO-2-BUTYL-3-BENZOFURANYL)(4-(3-(DIBUTYLAMINO)PROPOXY)PHENYL)METHANONE

METABOLITE (PARENT)


					4QS7YH22HT

(2S,3S,4S,5R,6S)-6-(4-(3-(DIBUTYLAMINO)PROPOXY)BENZOYL)OXY-3,4,5-TRIHYDROXY-TETRAHYDROPYRAN-2-CARBOXYLIC ACID

METABOLITE LESS ACTIVE (PARENT)


					C3801M93QC

DEBUTYLDRONEDARONE

SALT/SOLVATE (PARENT)


					FA36DV299Q

DRONEDARONE HYDROCHLORIDE