ACEBUTOLOL

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C18H28N2O4
Molecular Weight	336.4259
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ACEBUTOLOL

Structure Search

SMILES

CCCC(=O)NC1=CC(C(C)=O)=C(OCC(O)CNC(C)C)C=C1

InChI

InChIKey=GOEMGAFJFRBGGG-UHFFFAOYSA-N

InChI=1S/C18H28N2O4/c1-5-6-18(23)20-14-7-8-17(16(9-14)13(4)21)24-11-15(22)10-19-12(2)3/h7-9,12,15,19,22H,5-6,10-11H2,1-4H3,(H,20,23)

HIDE SMILES / InChI

Molecular Formula	C18H28N2O4
Molecular Weight	336.4259
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:40:21 UTC 2023` Edited by `admin` on `Fri Dec 15 17:40:21 UTC 2023`
Record UNII	67P356D8GH
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

ACEBUTOLOL

Official Name

English

C07AB04

Code

English

Acebutolol [WHO-DD]

Common Name

English

BUTANAMIDE, N-(3-ACETYL-4-(2-HYDROXY-3-((1-METHYLETHYL)AMINO)PROPOXY)PHENYL)-, (±)-

Systematic Name

English

acebutolol [INN]

Common Name

English

ACEBUTOLOL [VANDF]

Common Name

English

ACEBUTOLOL [MI]

Common Name

English

ACEBUTOLOL [USAN]

Common Name

English

ACEBUTOLOL [MART.]

Common Name

English

(±)-3'-ACETYL-4'-(2-HYDROXY-3-(ISOPROPYLAMINO)PROPOXY)BUTYRANILIDE

Systematic Name

English

Classification Tree Code System Code

WHO-ATC

C07AB04

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

NDF-RT

N0000175556

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

NDF-RT

N0000000161

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

WHO-VATC

QC07AB04

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

LIVERTOX

NBK548853

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

WHO-ATC

C07BB04

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

NCI_THESAURUS

C29576

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

Code System Code Type Description

INN

3295

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

MESH

D000070

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

NCI_THESAURUS

C61525

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

PUBCHEM

1978

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

DAILYMED

67P356D8GH

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

ECHA (EC/EINECS)

253-539-0

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

DRUG BANK

DB01193

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

SMS_ID

100000092351

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

RXCUI

149

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

RxNorm

EVMPD

SUB07371MIG

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

MERCK INDEX

m1290

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

Merck Index

LACTMED

Acebutolol

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

FDA UNII

67P356D8GH

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

CHEBI

2379

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

EPA CompTox

DTXSID2048539

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

CAS

37517-30-9

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

ChEMBL

CHEMBL642

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

DRUG CENTRAL

40

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

WIKIPEDIA

ACEBUTOLOL

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

IUPHAR

7107

Created by admin on Fri Dec 15 17:40:21 UTC 2023 , Edited by admin on Fri Dec 15 17:40:21 UTC 2023

PRIMARY

Related Record Type Details


					1QW38XEE0N

ACEBUTOLOL, (S)-

ENANTIOMER -> RACEMATE


					B025Y34C54

ACEBUTOLOL HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					4A4MK4KIB5

BETA-1 ADRENERGIC RECEPTOR

TARGET -> AGONIST

Interaction Type:

SHORT-ACTING

Amount:


					856NOF5HE9

ACEBUTOLOL, (R)-

ENANTIOMER -> RACEMATE


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:

Related Record Type Details


					2JZ6BC3K11

DEACYL ACEBUTOLOL

METABOLITE -> PARENT

Qualification:

PLASMA; URINE


					4ER0CZ5G7C

METABOLITE ACTIVE -> PARENT

Interaction Type:

MAJOR

Qualification:

PLASMA; URINE

Related Record Type Details


					67P356D8GH

ACTIVE MOIETY

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Volume of Distribution	PHARMACOKINETIC

Biological Half-life	PHARMACOKINETIC