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Details

Stereochemistry RACEMIC
Molecular Formula C18H29NO3
Molecular Weight 307.4278
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BETAXOLOL

SMILES

CC(C)NCC(O)COC1=CC=C(CCOCC2CC2)C=C1

InChI

InChIKey=NWIUTZDMDHAVTP-UHFFFAOYSA-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

HIDE SMILES / InChI

Molecular Formula C18H29NO3
Molecular Weight 307.4278
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 15:38:15 UTC 2023
Edited
by admin
on Fri Dec 15 15:38:15 UTC 2023
Record UNII
O0ZR1R6RZ2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BETAXOLOL
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
2-PROPANOL, 1-(4-(2-(CYCLOPROPYLMETHOXY)ETHYL)PHENOXY)-3-((1-METHYLETHYL)AMINO)-
Systematic Name English
betaxolol [INN]
Common Name English
SL-7521210 FREE BASE
Code English
BETAXOLOL [MI]
Common Name English
ALO-140102 FREE BASE
Code English
Betaxolol [WHO-DD]
Common Name English
BETAXOLOL [VANDF]
Common Name English
Classification Tree Code System Code
WHO-VATC QS01ED52
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
LIVERTOX NBK548618
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
WHO-VATC QS01ED02
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
WHO-ATC C07AB05
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
NDF-RT N0000000161
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
WHO-VATC QC07AB05
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
NDF-RT N0000175556
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
WHO-ATC S01ED02
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
WHO-ATC S01ED52
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
Code System Code Type Description
EVMPD
SUB05804MIG
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
INN
4530
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
MESH
D015784
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
IUPHAR
549
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
WIKIPEDIA
BETAXOLOL
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
LACTMED
Betaxolol
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
PUBCHEM
2369
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL423
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
NCI_THESAURUS
C61652
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
FDA UNII
O0ZR1R6RZ2
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
MERCK INDEX
m2454
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY Merck Index
RXCUI
1520
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY RxNorm
CHEBI
3082
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
SMS_ID
100000092503
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
DAILYMED
O0ZR1R6RZ2
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
CAS
63659-18-7
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
DRUG CENTRAL
356
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID2022674
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
DRUG BANK
DB00195
Created by admin on Fri Dec 15 15:38:15 UTC 2023 , Edited by admin on Fri Dec 15 15:38:15 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SHORT-ACTING
ENANTIOMER -> RACEMATE
BINDER->LIGAND
BINDING
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC