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Details

Stereochemistry RACEMIC
Molecular Formula C14H16N2O3.ClH
Molecular Weight 296.749
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NADOXOLOL HYDROCHLORIDE

SMILES

Cl.ONC(=N)CC(O)COC1=CC=CC2=C1C=CC=C2

InChI

InChIKey=QMIHLTWUCXXBQQ-UHFFFAOYSA-N
InChI=1S/C14H16N2O3.ClH/c15-14(16-18)8-11(17)9-19-13-7-3-5-10-4-1-2-6-12(10)13;/h1-7,11,17-18H,8-9H2,(H2,15,16);1H

HIDE SMILES / InChI

Molecular Formula C14H16N2O3
Molecular Weight 260.2884
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Nadoxolol is a beta-adrenergic blocking agent and an antihypertensive drug.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Clinical study of a new anti-arrhythmia agent: nadoxolol].
1976 Apr
[Acute nadoxolol poisoning. A multicentric study of 35 cases].
1982 May
Kinetic resolution of 1-chloro-3-(1-naphthyloxy)-2-propanol, an intermediate in the synthesis of beta-adrenergic receptor blockers.
2003 Jun
Patents

Sample Use Guides

LD50 in mice (mg/kg): 180 i.v.; 1000 orally
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:41:09 GMT 2023
Edited
by admin
on Fri Dec 15 20:41:09 GMT 2023
Record UNII
RZ9G589EN2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NADOXOLOL HYDROCHLORIDE
JAN   MART.   MI   WHO-DD  
Common Name English
NADOXOLOL HYDROCHLORIDE [MI]
Common Name English
Nadoxolol hydrochloride [WHO-DD]
Common Name English
BRADYL
Brand Name English
LL-1530
Code English
NADOXOLOL HYDROCHLORIDE [MART.]
Common Name English
BUTANIMIDAMIDE, N,3-DIHYDROXY-4-(1-NAPHTHALENYLOXY)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
CAS
35991-93-6
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
PUBCHEM
88709809
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
RXCUI
236178
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID10957415
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
MERCK INDEX
m1212
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
252-825-2
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
FDA UNII
RZ9G589EN2
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
EVMPD
SUB03370MIG
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
SMS_ID
100000085705
Created by admin on Fri Dec 15 20:41:09 GMT 2023 , Edited by admin on Fri Dec 15 20:41:09 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE