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

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H29NO3
Molecular Weight 307.4278
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOBETAXOLOL

SMILES

CC(C)NC[C@H](O)COC1=CC=C(CCOCC2CC2)C=C1

InChI

InChIKey=NWIUTZDMDHAVTP-KRWDZBQOSA-N
InChI=1S/C18H29NO3/c1-14(2)19-11-17(20)13-22-18-7-5-15(6-8-18)9-10-21-12-16-3-4-16/h5-8,14,16-17,19-20H,3-4,9-13H2,1-2H3/t17-/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H29NO3
Molecular Weight 307.4278
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:29:20 UTC 2023
Edited
by admin
on Fri Dec 15 16:29:20 UTC 2023
Record UNII
75O9XHA4TU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOBETAXOLOL
INN  
INN  
Official Name English
Levobetaxolol [WHO-DD]
Common Name English
BETAXOLOL, (S)-
Common Name English
levobetaxolol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
Code System Code Type Description
RXCUI
353497
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL1201274
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
SMS_ID
100000082805
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
IUPHAR
8035
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
CHEBI
59254
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
NCI_THESAURUS
C66006
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID30239341
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
DRUG BANK
DB09351
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
WIKIPEDIA
Levobetaxolol
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
PUBCHEM
60657
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
EVMPD
SUB08462MIG
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
FDA UNII
75O9XHA4TU
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
CAS
93221-48-8
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
DRUG CENTRAL
4752
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
INN
6447
Created by admin on Fri Dec 15 16:29:20 UTC 2023 , Edited by admin on Fri Dec 15 16:29:20 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY