Chemical compound
Pharmaceutical compound
Timolol Trade names Timoptic, others[ 1] AHFS /Drugs.com Maleate Monograph eent Monograph MedlinePlus a684029 License data
Pregnancy category Routes of administration By mouth , topical (eye drop )Drug class Beta blocker ATC code Legal status
Bioavailability 60% Metabolism Liver (80%, mainly CYP2D6 [ 4] )Onset of action 15–30 min[ 3] Elimination half-life 2.5–5 hours Duration of action 24 hours[ 3] Excretion Kidney
(S )-1-(tert -Butylamino)-3-[(4-morpholin-4-yl-1,2,5-thiadiazol-3-yl)oxy]propan-2-ol
CAS Number PubChem CID IUPHAR/BPS DrugBank ChemSpider UNII KEGG ChEBI ChEMBL CompTox Dashboard (EPA ) ECHA InfoCard 100.043.651 Formula C 13 H 24 N 4 O 3 S Molar mass 316.42 g·mol−1 3D model (JSmol )
CC(C)(C)NCC(O)COc1nsnc1N1CCOCC1
InChI=1S/C13H24N4O3S/c1-13(2,3)14-8-10(18)9-20-12-11(15-21-16-12)17-4-6-19-7-5-17/h10,14,18H,4-9H2,1-3H3/t10-/m0/s1
Y Key:BLJRIMJGRPQVNF-JTQLQIEISA-N
Y
(verify)
Timolol is a beta blocker medication used either by mouth or as eye drops .[ 3] [ 5] As eye drops it is used to treat increased pressure inside the eye such as in ocular hypertension and glaucoma .[ 3] By mouth it is used for high blood pressure , chest pain due to insufficient blood flow to the heart , to prevent further complications after a heart attack , and to prevent migraines .[ 5]
Common side effects with the drops is irritation of the eye.[ 3] Common side effects by mouth include tiredness, slow heart beat , itchiness, and shortness of breath .[ 5] Other side effects include masking the symptoms of low blood sugar in those with diabetes .[ 3] Use is not recommended in those with asthma , uncompensated heart failure , or chronic obstructive pulmonary disease (COPD).[ 3] It is unclear if use during pregnancy is safe for the fetus.[ 6] Timolol is a non-selective beta blocker .[ 3]
Timolol was patented in 1968, and came into medical use in 1978.[ 7] It is on the World Health Organization's List of Essential Medicines .[ 8] Timolol is available as a generic medication .[ 3] [ 9] In 2023, it was the 173rd most commonly prescribed medication in the United States, with more than 2 million prescriptions.[ 10] [ 11]
Medical uses
By mouth
In its by mouth or oral form, it is used:
The combination of timolol and the alpha-1 blocker prazosin has sedative effects.[ 13]
Eye drops
In its eye drop form it is used to treat open-angle and, occasionally, secondary glaucoma .[ 3] [ 14] The mechanism of action of timolol is probably the reduction of the formation of aqueous humor[ 3] in the ciliary body in the eye. It was the first beta blocker approved for topical use in treatment of glaucoma in the United States (1978).[ 15] When used by itself, it depresses intraocular pressure (IOP) 18–34% below baseline within first few treatments. However, there are short-term escape and long-term drift effects in some people. That is, tolerance develops. It may reduce the extent of the daytime IOP curve up to 50%. The IOP is higher during sleep. Efficacy of timolol in lowering IOP during the sleep period may be limited.[ 16] [ 17] [ 18] It is a 5–10× more potent beta blocker than propranolol . Timolol is light-sensitive; it is usually preserved with 0.01% benzalkonium chloride (BAC), but also comes BAC-free. It can also be used in combination with pilocarpine , carbonic anhydrase inhibitors [ 19] or prostaglandin analogs.[ 20]
A Cochrane review compared the effect of timolol versus brimonidine in slowing the progression of open angle glaucoma in adults but found insufficient evidence to come to conclusions.[ 21]
On the skin
In its gel form it is used on the skin to treat infantile hemangiomas .[ 22]
It is available in tablet and liquid formulations.[ 23] [ 24]
For ophthalmic use, timolol is also available combined:
Contraindications
The medication should not be taken by individuals with:[ 23]
Side effects
The most serious possible side effects include cardiac arrhythmias and severe bronchospasms .[ 23] Timolol can also lead to fainting , congestive heart failure , depression , confusion , worsening of Raynaud's syndrome and impotence .[ 23]
Side effects when given in the eye include: burning sensation, eye redness, superficial punctate keratopathy, corneal numbness.[ 24] [ 14]
Chemistry
The experimental log P of timolol is 1.8 and its predicted log P ranges from 0.68 to 1.8.[ 26] [ 27] [ 28]
Society and culture
Brand names
Timolol is sold under many brand names worldwide.[ 1] Timolol eye drops are sold under the brand names Timoptic and Istalol among others.[ 29] [ 30]
References
^ a b "Timolol" . Drugs.com . Archived from the original on 7 March 2016. Retrieved 28 December 2016 .
^ "Product monograph brand safety updates" . Health Canada . February 2024. Retrieved 24 March 2024 .
^ a b c d e f g h i j k "Timolol eent" . The American Society of Health-System Pharmacists. Archived from the original on 28 December 2016. Retrieved 8 December 2016 .
^ Volotinen M, Turpeinen M, Tolonen A, Uusitalo J, Mäenpää J, Pelkonen O (July 2007). "Timolol metabolism in human liver microsomes is mediated principally by CYP2D6". Drug Metabolism and Disposition . 35 (7): 1135– 1141. doi :10.1124/dmd.106.012906 . PMID 17431033 . S2CID 794764 .
^ a b c "Timolol Maleate" . The American Society of Health-System Pharmacists. Archived from the original on 28 December 2016. Retrieved 8 December 2016 .
^ "Timolol ophthalmic Use During Pregnancy" . The American Society of Health-System Pharmacists. Archived from the original on 28 December 2016. Retrieved 28 December 2016 .
^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery . John Wiley & Sons. p. 460. ISBN 9783527607495 . Archived from the original on 28 December 2016.
^ World Health Organization (2023). The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023) . Geneva: World Health Organization. hdl :10665/371090 . WHO/MHP/HPS/EML/2023.02.
^ "Competitive Generic Therapy Approvals" . U.S. Food and Drug Administration (FDA) . 29 June 2023. Archived from the original on 29 June 2023. Retrieved 29 June 2023 .
^ "Top 300 of 2023" . ClinCalc . Archived from the original on 12 August 2025. Retrieved 12 August 2025 .
^ "Timolol Drug Usage Statistics, United States, 2013 - 2023" . ClinCalc . Retrieved 19 August 2025 .
^ Marcus DA, Bain PA (27 February 2009). Effective Migraine Treatment in Pregnant and Lactating Women: A Practical Guide . シュプリンガー・ジャパン株式会社. pp. 141–. ISBN 978-1-60327-438-8 . Archived from the original on 5 November 2017. Retrieved 14 November 2010 .
^ Atkin T, Comai S, Gobbi G (April 2018). "Drugs for Insomnia beyond Benzodiazepines: Pharmacology, Clinical Applications, and Discovery" . Pharmacol Rev . 70 (2): 197– 245. doi :10.1124/pr.117.014381 . PMID 29487083 . S2CID 3578916 .
^ a b "Timolol Ophthalmic" . MedlinePlus . 15 April 2017. Retrieved 31 December 2019 .
^ Sambhara D, Aref AA (January 2014). "Glaucoma management: relative value and place in therapy of available drug treatments" . Therapeutic Advances in Chronic Disease . 5 (1): 30– 43. doi :10.1177/2040622313511286 . PMC 3871276 . PMID 24381726 .
^ Liu JH, Kripke DF, Weinreb RN (September 2004). "Comparison of the nighttime effects of once-daily timolol and latanoprost on intraocular pressure". American Journal of Ophthalmology . 138 (3): 389– 95. doi :10.1016/j.ajo.2004.04.022 . PMID 15364220 .
^ Liu JH, Medeiros FA, Slight JR, Weinreb RN (March 2009). "Comparing diurnal and nocturnal effects of brinzolamide and timolol on intraocular pressure in patients receiving latanoprost monotherapy". Ophthalmology . 116 (3): 449– 54. doi :10.1016/j.ophtha.2008.09.054 . PMID 19157559 .
^ Liu JH, Slight JR, Vittitow JL, Scassellati Sforzolini B, Weinreb RN (September 2016). "Efficacy of Latanoprostene Bunod 0.024% Compared With Timolol 0.5% in Lowering Intraocular Pressure Over 24 Hours" . American Journal of Ophthalmology . 169 : 249– 257. doi :10.1016/j.ajo.2016.04.019 . PMID 27457257 .
^ Strohmaier K, Snyder E, Adamsons I (July 1998). "A multicenter study comparing dorzolamide and pilocarpine as adjunctive therapy to timolol: patient preference and impact on daily life". Journal of the American Optometric Association . 69 (7): 441– 51. PMID 9697378 .
^ "Ganfort 0.3 mg/ml + 5 mg/ml eye drops, solution - Summary of Product Characteristics (SmPC)" . (emc) . 20 February 2020. Retrieved 1 March 2020 .
^ Sena DF, Lindsley K (January 2017). "Neuroprotection for treatment of glaucoma in adults" . The Cochrane Database of Systematic Reviews . 1 (1): CD006539. doi :10.1002/14651858.CD006539.pub4 . PMC 5370094 . PMID 28122126 . {{cite journal }}
: CS1 maint: article number as page number (link )
^ Novoa M, Baselga E, Beltran S, Giraldo L, Shahbaz A, Pardo-Hernandez H, et al. (April 2018). "Interventions for infantile haemangiomas of the skin" . The Cochrane Database of Systematic Reviews . 2018 (4): CD006545. doi :10.1002/14651858.CD006545.pub3 . PMC 6513200 . PMID 29667726 . {{cite journal }}
: CS1 maint: article number as page number (link )
^ a b c d "Timolol Maleate tablet" . DailyMed . 17 August 2006. Retrieved 1 December 2019 .
^ a b "Betimol- timolol solution" . DailyMed . 18 March 2010. Retrieved 1 December 2019 .
^ "Package leaflet: Information for the user Timolol" (PDF) . hpra.ie . Archived from the original (PDF) on 16 August 2018. Retrieved 15 August 2018 .
^ "Timolol | C13H24N4O3S | CID 33624 - PubChem" . pubchem.ncbi.nlm.nih.gov . Retrieved 2 August 2025 .
^ "(−)-S-Timolol" . ChemSpider . 10 June 2024. Retrieved 10 July 2025 .
^ "Timolol: Uses, Interactions, Mechanism of Action" . DrugBank Online . 31 December 1994. Retrieved 10 July 2025 .
^ "Generic Istalol Availability" . Drugs.com . Retrieved 20 June 2019 .
^ "Istalol" . Drugs.com . 1 August 2018. Retrieved 19 July 2019 .
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