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

Details

Stereochemistry ABSOLUTE
Molecular Formula C13H21NO3
Molecular Weight 239.3107
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOMOPROLOL

SMILES

COC1=CC=CC=C1OC[C@@H](O)CNC(C)C

InChI

InChIKey=LFTFGCDECFPSQD-NSHDSACASA-N
InChI=1S/C13H21NO3/c1-10(2)14-8-11(15)9-17-13-7-5-4-6-12(13)16-3/h4-7,10-11,14-15H,8-9H2,1-3H3/t11-/m0/s1

HIDE SMILES / InChI
Levomoprolol (L-moprolol) is a beta-adrenergic blocker which was introduced as an oral medication for treatment of systemic hypertension. It was found to be effective in 2% eyedrops in reducing the intraocular pressure in glaucoma. Observations on glaucoma patients treated with the eyedrop for 1.5 to 2.5 years was without undesirable side effects. L-moprolol and dipivefrin had an equivalent effect in lowering the intraocular pressure. The association of the two drugs caused a further reduction of intraocular pressure.

Approval Year

PubMed

PubMed

TitleDatePubMed
Tolerability of high doses of (-)-moprolol in healthy volunteers.
1982
[Effects of acute administration of the levogyral beta-blocker levomoprolol on the exercise test in angina pectoris].
1984 Dec
A new catalyst for the asymmetric Henry reaction: synthesis of β-nitroethanols in high enantiomeric excess.
2012 Dec 21
Patents
Name Type Language
LEVOMOPROLOL
INN  
INN  
Official Name English
MOPROLOL, (S)-
Common Name English
(-)-(S)-1-(ISOPROPYLAMINO)-3-(O-METHOXYPHENOXY)-2-PROPANOL
Common Name English
levomoprolol [INN]
Common Name English
MOPROLOL L-FORM
MI  
Common Name English
MOPROLOL, (-)-
Common Name English
MOPROLOL L-FORM [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
Code System Code Type Description
FDA UNII
K4NON6FSON
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
PRIMARY
SMS_ID
100000082279
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106030
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
PRIMARY
EVMPD
SUB08480MIG
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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CAS
77164-20-6
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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DRUG CENTRAL
3981
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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MERCK INDEX
m1207
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
PRIMARY Merck Index
INN
6150
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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EPA CompTox
DTXSID301016500
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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PUBCHEM
3034006
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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WIKIPEDIA
Levomoprolol
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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NCI_THESAURUS
C83877
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
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MESH
C009976
Created by admin on Sat Dec 16 17:56:17 GMT 2023 , Edited by admin on Sat Dec 16 17:56:17 GMT 2023
PRIMARY