Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H29NO3.ClH |
Molecular Weight | 343.889 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)NC[C@H](O)COC1=CC=C(CCOCC2CC2)C=C1
InChI
InChIKey=CHDPSNLJFOQTRK-LMOVPXPDSA-N
InChI=1S/C18H29NO3.ClH/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;1H/t17-;/m0./s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/19668496Curator's Comment: description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021114s003lbl.pdf
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19668496
Curator's Comment: description was created based on several sources, including
http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/021114s003lbl.pdf
BETAXON™ is a trade name for levobetaxolol hydrochloride ophthalmic suspension 0.5%, which is indicated for lowering intraocular pressure in patients with chronic open-angle glaucoma or ocular hypertension. The brand name Betaxon is discontinued in USA, but generic versions may be available. Levobetaxolol is a cardioselective (beta-1¬ adrenergic) receptor-blocking agent that does not have significant membrane-stabilizing (local anesthetic) activity and is devoid of intrinsic sympathomimetic action. Animal studies suggest levobetaxolol (S-isomer) is the more active enantiomer of betaxolol (racemate).
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL213 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19668496 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | BETAXON Approved UseBETAXON™ (levobetaxolol hydrochloride ophthalmic suspension) 0.5% is indicated for lowering intraocular pressure in patients with
chronic open-angle glaucoma or ocular hypertension. Launch Date2000 |
|||
Primary | BETAXON Approved UseBETAXON™ (levobetaxolol hydrochloride ophthalmic suspension) 0.5% is indicated for lowering intraocular pressure in patients with
chronic open-angle glaucoma or ocular hypertension. Launch Date2000 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
4.7 ng/g |
1 drop 2 times / day multiple, ocular dose: 1 drop route of administration: Ocular experiment type: MULTIPLE co-administered: |
LEVOBETAXOLOL plasma | Oryctolagus cuniculus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.5 ng/mL |
1 drop 2 times / day steady-state, ocular dose: 1 drop route of administration: Ocular experiment type: STEADY-STATE co-administered: |
LEVOBETAXOLOL plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
10.4 ng × h/g |
1 drop 2 times / day multiple, ocular dose: 1 drop route of administration: Ocular experiment type: MULTIPLE co-administered: |
LEVOBETAXOLOL plasma | Oryctolagus cuniculus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
1.6 h |
1 drop 2 times / day multiple, ocular dose: 1 drop route of administration: Ocular experiment type: MULTIPLE co-administered: |
LEVOBETAXOLOL plasma | Oryctolagus cuniculus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
20 h |
1 drop 2 times / day steady-state, ocular dose: 1 drop route of administration: Ocular experiment type: STEADY-STATE co-administered: |
LEVOBETAXOLOL plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
48% |
1 drop 2 times / day multiple, ocular dose: 1 drop route of administration: Ocular experiment type: MULTIPLE co-administered: |
LEVOBETAXOLOL plasma | Oryctolagus cuniculus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Doses
Dose | Population | Adverse events |
---|---|---|
0.5 % 2 times / day steady, ophthalmic Recommended Dose: 0.5 %, 2 times / day Route: ophthalmic Route: steady Dose: 0.5 %, 2 times / day Sources: |
unhealthy, 1 - 6 years n = 48 Health Status: unhealthy Condition: pediatric glaucomas Age Group: 1 - 6 years Sex: M+F Population Size: 48 Sources: |
Other AEs: Eye disorders NEC, Bradycardia... Other AEs: Eye disorders NEC (6 patients) Sources: Bradycardia (1 patient) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Bradycardia | 1 patient | 0.5 % 2 times / day steady, ophthalmic Recommended Dose: 0.5 %, 2 times / day Route: ophthalmic Route: steady Dose: 0.5 %, 2 times / day Sources: |
unhealthy, 1 - 6 years n = 48 Health Status: unhealthy Condition: pediatric glaucomas Age Group: 1 - 6 years Sex: M+F Population Size: 48 Sources: |
Eye disorders NEC | 6 patients | 0.5 % 2 times / day steady, ophthalmic Recommended Dose: 0.5 %, 2 times / day Route: ophthalmic Route: steady Dose: 0.5 %, 2 times / day Sources: |
unhealthy, 1 - 6 years n = 48 Health Status: unhealthy Condition: pediatric glaucomas Age Group: 1 - 6 years Sex: M+F Population Size: 48 Sources: |
Sample Use Guides
The recommended dose is one drop of BETAXON™ (levobetaxolol hydrochloride
ophthalmic suspension) 0.5% in the affected eye(s) twice daily. In some patients, the intraocular pressure lowering responses to BETAXONTM Ophthalmic Suspension may require a few weeks to stabilize.
Route of Administration:
Other
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29576
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admin on Fri Dec 15 15:36:35 GMT 2023 , Edited by admin on Fri Dec 15 15:36:35 GMT 2023
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CHEMBL1201274
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DBSALT001395
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60656
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DTXSID20151321
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116209-55-3
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261718
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AA-114
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8MR4W4O06J
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C66007
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ACTIVE MOIETY
SUBSTANCE RECORD