BUPRANOLOL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C14H22ClNO2
Molecular Weight	271.783
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BUPRANOLOL

Structure Search

SMILES

CC1=CC(OCC(O)CNC(C)(C)C)=C(Cl)C=C1

InChI

InChIKey=HQIRNZOQPUAHHV-UHFFFAOYSA-N

InChI=1S/C14H22ClNO2/c1-10-5-6-12(15)13(7-10)18-9-11(17)8-16-14(2,3)4/h5-7,11,16-17H,8-9H2,1-4H3

HIDE SMILES / InChI

Molecular Formula	C14H22ClNO2
Molecular Weight	271.783
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 16:47:17 UTC 2023` Edited by `admin` on `Fri Dec 15 16:47:17 UTC 2023`
Record UNII	858YGI5PIT
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

BUPRANOLOL

Official Name

English

B-1312 FREE BASE

Code

English

KL-255 FREE BASE

Code

English

Bupranolol [WHO-DD]

Common Name

English

B 1312 FREE BASE

Code

English

OPHTORENIN

Brand Name

English

1-(TERT-BUTYLAMINO)-3-((6-CHLORO-M-TOLYL)-OXY)-2-PROPANOL

Systematic Name

English

BUPRANOLOL [MI]

Common Name

English

bupranolol [INN]

Common Name

English

BUPRANOL

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C29576

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

WHO-VATC

QC07AA19

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

WHO-ATC

C07AA19

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

Code System Code Type Description

DRUG CENTRAL

433

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

IUPHAR

550

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

WIKIPEDIA

Bupranolol

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

CAS

14556-46-8

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

SMS_ID

100000088467

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

FDA UNII

858YGI5PIT

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

MESH

D002046

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

CAS

70578-42-6

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

SUPERSEDED

INN

3166

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

EVMPD

SUB05984MIG

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

DRUG BANK

DB08808

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

RXCUI

1817

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

RxNorm

EPA CompTox

DTXSID7022704

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

ChEMBL

CHEMBL305380

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

PUBCHEM

2475

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

NCI_THESAURUS

C72615

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

MERCK INDEX

m2770

Created by admin on Fri Dec 15 16:47:17 UTC 2023 , Edited by admin on Fri Dec 15 16:47:17 UTC 2023

PRIMARY

Merck Index

Related Record Type Details


					94461Q7T5J

BUPRANOLOL, (R)-

ENANTIOMER -> RACEMATE


					DTC2G3GDPL

BUPRANOLOL HYDROCHLORIDE

SALT/SOLVATE -> PARENT


					H6YMB4FH7P

BUPRANOLOL, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					858YGI5PIT

ACTIVE MOIETY