U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C15H19NO
Molecular Weight 229.3175
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PRONETALOL

SMILES

CC(C)NCC(O)C1=CC=C2C=CC=CC2=C1

InChI

InChIKey=HRSANNODOVBCST-UHFFFAOYSA-N
InChI=1S/C15H19NO/c1-11(2)16-10-15(17)14-8-7-12-5-3-4-6-13(12)9-14/h3-9,11,15-17H,10H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C15H19NO
Molecular Weight 229.3175
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 Sat Dec 16 17:50:09 UTC 2023
Edited
by admin
on Sat Dec 16 17:50:09 UTC 2023
Record UNII
XBP4RT1IMQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRONETALOL
INN   WHO-DD  
INN  
Official Name English
AY-6204 FREE BASE
Code English
Pronetalol [WHO-DD]
Common Name English
NETHALIDE
Common Name English
2-ISOPROPYLAMINO-1-(NAPHTH-2-YL)ETHANOL
Systematic Name English
NETH
Common Name English
COMPOUND 38174
Code English
DL-PRONETHALOL
Common Name English
GNF-PF-2670
Code English
ICI 38174 FREE BASE
Code English
PRONETHALOL [MI]
Common Name English
PRONETHALOL
MI  
Common Name English
AY-6204 HCL
Code English
pronetalol [INN]
Common Name English
NAPHTHYLISOPROTERENOL
Common Name English
ICI-38174 FREE BASE
Code English
INETOL
Brand Name English
AY 6204 FREE BASE
Code English
2-NAPHTHALENEMETHANOL, .ALPHA.-(((1-METHYLETHYL)AMINO)METHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID8021193
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
WIKIPEDIA
Pronethalol
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
CAS
54-80-8
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
SMS_ID
100000081148
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
DRUG CENTRAL
2289
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
FDA UNII
XBP4RT1IMQ
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
EVMPD
SUB10092MIG
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
PUBCHEM
4930
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
MERCK INDEX
m1239
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C82257
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
MESH
C084832
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
ChEMBL
CHEMBL16476
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
INN
1580
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
PRIMARY
CAS
2238-85-9
Created by admin on Sat Dec 16 17:50:09 UTC 2023 , Edited by admin on Sat Dec 16 17:50:09 UTC 2023
SUPERSEDED
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY