Latanoprost
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Also known as CatiolanzeIyuzehLatanoprost (isopropyl ester)Latanoprost component of rocklatanLatanoprost component of xalacomMonopostPHXA-41PHXA41T-2345T2345XA-41XA41XalatanXelprosLanatoprostSID26719861LatonoprostC0164737
Summary
Latanoprost (CHEMBL1051) is an approved small-molecule antiglaucoma drug (ATC S01EE01) targeting PTGFR; indicated across 7 conditions including open-angle glaucoma and ocular hypertension.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: S01EE01
- Targets: 1 (PTGFR)
- Indications: 7 conditions
- Clinical trials: 154
- Chemistry: 432.6 Da · C26H40O5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1051 |
| Name | Latanoprost |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 5311221 |
| ChEBI | CHEBI:6384 |
| ATC | S01EE01 |
| Molecular formula | C26H40O5 |
| Molecular weight | 432.6 |
| InChIKey | GGXICVAJURFBLW-CEYXHVGTSA-N |
SMILES: CC(C)OC(=O)CCC/C=C\C[C@H]1[C@H](C[C@H]([C@@H]1CC[C@H](CCC2=CC=CC=C2)O)O)O
IUPAC name: propan-2-yl (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(3R)-3-hydroxy-5-phenylpentyl]cyclopentyl]hept-5-enoate
ChEBI definition: A prostaglandin Fα that is the isopropyl ester prodrug of latanoprost free acid. Used in the treatment of open-angle glaucoma and ocular hypertension.
Pharmacological roles (ChEBI): antiglaucoma drug, antihypertensive agent, EC 4.2.1.1 (carbonic anhydrase) inhibitor, prodrug.
Also known as: Catiolanze, Iyuzeh, Latanoprost, Latanoprost (isopropyl ester), Latanoprost component of rocklatan, Latanoprost component of xalacom, Monopost, PHXA-41, PHXA41, T-2345, T2345, XA-41
Patent coverage: 3,721 distinct patent families (14,975 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| PTGFR | FP receptor | Full agonist | 6.3 | 0% | P43088 |
Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Microtubule-associated protein tau, Lysine-specific demethylase 4E, Menin/Histone-lysine N-methyltransferase MLL, Mitogen-activated protein kinase 1, Bile salt export pump.
Bioactivity
ChEMBL activities: 1 potent at pChembl ≥ 5 of 5 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| MAPT | 5.3 | Potency | 5012 | nM | CHEMBL_ACT_4012935 |
Target pathways
Aggregated over 1 target gene(s): PTGFR.
Top Reactome pathways
2 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Prostanoid ligand receptors | 1 | PTGFR |
| G alpha (q) signalling events | 1 | PTGFR |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| inflammatory response | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| adenylate cyclase-activating G protein-coupled receptor signaling pathway | 1 |
| positive regulation of cytosolic calcium ion concentration | 1 |
| parturition | 1 |
| positive regulation of cell population proliferation | 1 |
| positive regulation of gene expression | 1 |
| response to estradiol | 1 |
| response to lipopolysaccharide | 1 |
| negative regulation of apoptotic process | 1 |
| cellular response to prostaglandin D stimulus | 1 |
| signal transduction | 1 |
| response to lipid | 1 |
Indications & clinical
Indications
7 indications (4 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| open-angle glaucoma | 4 | MONDO:0005338 | EFO:0004190 |
| ocular hypertension | 4 | MONDO:0006875 | EFO:1001069 |
| hypertensive disorder | 4 | MONDO:0005044 | EFO:0000537 |
| glaucoma | 4 | MONDO:0005041 | MONDO:0005041 |
| Meniere disease | 2 | MONDO:0007972 | EFO:0006862 |
| vitiligo | 2 | MONDO:0008661 | EFO:0004208 |
| alopecia areata | 1 | MONDO:0005340 | EFO:0004192 |
Clinical trials
Total trials: 154.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 55 |
| PHASE3 | 32 |
| PHASE2 | 29 |
| Not specified | 19 |
| PHASE1 | 7 |
| PHASE1/PHASE2 | 6 |
| PHASE2/PHASE3 | 3 |
| EARLY_PHASE1 | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04957329 | PHASE4 | RECRUITING | Effect of Benzalkonium Chloride Preserved and Preservative-free Latanoprost Eye Drops on Conjunctival Goblet Cells |
| NCT06883123 | PHASE4 | RECRUITING | Efficacy of Simbrinza and Rocklatan vs Cosopt and Latanoprost |
| NCT07048886 | PHASE4 | NOT_YET_RECRUITING | Rocklatan Adds Pressure Reduction After MIGS (Minimally Invasive Glaucoma Surgery) |
| NCT07325240 | PHASE4 | RECRUITING | 24-hour Effect of Rocklatan Compared With Latanoprost in Open Angle Glaucoma and Ocular Hypertension Patients |
| NCT07465913 | PHASE4 | RECRUITING | Rocklatan vs Latanoprost Post-DSLT |
| NCT00140062 | PHASE4 | COMPLETED | Efficacy And Safety Of Xalatan Compared To Usual Care In Patients With Open Angle Glaucoma Or Ocular Hypertension. |
| NCT00224289 | PHASE4 | COMPLETED | Effect of Age on Latanoprost 0.005% in Patients With Glaucoma |
| NCT00273429 | PHASE4 | COMPLETED | Cosopt Versus Xalatan |
| NCT00273481 | PHASE4 | COMPLETED | Cosopt Versus Xalacom |
| NCT00304785 | PHASE4 | COMPLETED | Latanoprost Versus Fotil |
| NCT00308945 | PHASE4 | COMPLETED | Influence of Prostaglandins on Ocular Blood Flow in Glaucoma Patients |
| NCT00329095 | PHASE4 | COMPLETED | An Evaluation of Use of Topical Ocular Hypotensive Medication by Compliance |
| NCT00330577 | PHASE4 | COMPLETED | 24-Hour Intraocular Pressure (IOP) And Blood Pressure Control In Glaucoma And Ocular Hypertension Patients |
| NCT00348400 | PHASE4 | COMPLETED | Brimonidine Purite 0.15% Versus Dorzolamide 2% Used as Adjunctive Therapy to Latanoprost |
| NCT00440141 | PHASE4 | COMPLETED | Brimonidine 0.1% Versus Brinzolamide 1% as Adjunctive Therapy to Latanoprost 0.005% |
| NCT00539526 | PHASE4 | COMPLETED | Evaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues |
| NCT00541242 | PHASE4 | COMPLETED | Safety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With Glaucoma or Ocular Hypertension |
| NCT00647101 | PHASE4 | COMPLETED | A Study to Assess the Efficacy of 3 Months of Latanoprost Treatment in Reducing the Intraocular Pressure in Patients With Ocular Hypertension or Open-angle Glaucoma |
| NCT00705757 | PHASE4 | COMPLETED | The Effects of Xalatan, Travatan and Lumigan on Skin Pigmentation Near the Eye |
| NCT00735449 | PHASE4 | COMPLETED | Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in Glaucoma or Ocular Hypertension Subjects |
| NCT00757835 | PHASE4 | COMPLETED | 24-hr IOP With Travoprost/Timolol Compared With Latanoprost/Timolol in XFG |
| NCT00759941 | PHASE4 | COMPLETED | A Comparison of Azopt Versus Placebo Added to Xalatan in Patients With Elevated Intraocular Pressure (IOP) on a Prostaglandin |
| NCT00796198 | PHASE4 | UNKNOWN | Effects of Cosopt on IOP and on Ocular Diastolic Perfusion Pressure |
| NCT00798694 | PHASE4 | COMPLETED | How Similar Are Changes to the Surface of the Eye When Two Different Glaucoma Eye Drops Are Used? |
| NCT00799682 | PHASE4 | COMPLETED | Exploratory Study Comparing Signs and Symptoms in Patients With Ocular Hypertension or Glaucoma Using Xalatan R® or Travatan Z® |
| NCT00811564 | PHASE4 | COMPLETED | An Evaluation of the Fixed Combination Brimonidine Tartrate 0.2%/ Timolol Maleate 0.5% to Latanoprost 0.005% in Glaucoma or Ocular Hypertension Subjects |
| NCT00847483 | PHASE4 | COMPLETED | Comparison of Latanoprost With Travoprost and Bimatoprost in Patients With Elevated IOP. A 12-weeks, Masked Evaluator, Phase IV Multi-center Study in the US |
| NCT00906594 | PHASE4 | COMPLETED | Additive Intra-ocular Pressure Reduction Effect of Fixed Combination of Maleate Timolol 0.5%/Dorzolamide 2% on Monotherapy With Latanoprost in Patients With Elevated Intra-ocular Pressure |
| NCT00913029 | PHASE4 | COMPLETED | Evaluation of the iStent Versus Two Ocular Hypotensive Agents in Patients With Primary Open-angle Glaucoma (POAG) |
| NCT00941525 | PHASE4 | COMPLETED | Central Corneal Thickness and 24-hour Fluctuation of Intraocular Pressure |
| NCT01151904 | PHASE4 | TERMINATED | Study of Brimonidine and Timolol Ophthalmic Solution With Latanoprost Compared With Latanoprost in Glaucoma Patients |
| NCT01155219 | PHASE4 | COMPLETED | Safety, Efficacy Assessment of Geltim LP® 1 mg/g in Ocular Hypertensive or Glaucomatous Patients. |
| NCT01162603 | PHASE4 | COMPLETED | Latanoprost Versus Tafluprost: 24-hour Intraocular Pressure (IOP) |
| NCT01225653 | PHASE4 | COMPLETED | Topical Application of Latanoprost in Diabetic Retinopathy |
| NCT01243567 | PHASE4 | COMPLETED | Safety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost in Patients With Open-Angle Glaucoma Who Have Never Been Treated |
| NCT01315574 | PHASE4 | TERMINATED | Effects of Anti-Glaucoma Medications on the Ocular Surface |
| NCT01448837 | PHASE4 | COMPLETED | 24-Hour Intraocular Pressure Control With Bimatoprost/Timolol Versus Latanoprost as First Choice |
| NCT01525173 | PHASE4 | COMPLETED | A Safety and Efficacy Study of ALPHAGAN® P and LUMIGAN® in Subjects Previously Treated With Latanoprost for Glaucoma and Ocular Hypertension |
| NCT01655758 | PHASE4 | COMPLETED | 24-hour Control of Intraocular Pressure (IOP) in Ocular Hypertension |
| NCT01779284 | PHASE4 | COMPLETED | Travoprost/Timolol vs Latanoprost/Timolol Fixed Combination Therapy |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
13 molecules share ≥1 primary target. Top 13 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| DINOPROST | ChEMBL + PubChem | Phase 4 (approved) | PTGFR |
| DINOPROSTONE | ChEMBL + PubChem | Phase 4 (approved) | PTGFR |
| LAROPIPRANT | ChEMBL | Phase 4 (approved) | PTGFR |
| SEPETAPROST | ChEMBL | Phase 3 | PTGFR |
| CLOPROSTENOL | ChEMBL + PubChem | Phase 2 (approved) | PTGFR |
| EBOPIPRANT | ChEMBL | Phase 2 | PTGFR |
| FLUPROSTENOL | ChEMBL | Phase 2 | PTGFR |
| Belzutifan | PubChem | Approved | PTGFR |
| Bimatoprost | PubChem | Approved | PTGFR |
| Grapiprant | PubChem | Approved | PTGFR |
| Latanoprostene Bunod | PubChem | Approved | PTGFR |
| Nitroglycerin | PubChem | Approved | PTGFR |
| Tafluprost | PubChem | Approved | PTGFR |
Related Atlas pages
- Genes: PTGFR
- Diseases: open-angle glaucoma, ocular hypertension, hypertensive disorder, glaucoma
- Drugs: Dinoprost, Dinoprostone, Laropiprant, Sepetaprost, Belzutifan, Bimatoprost, Latanoprostene Bunod, Nitroglycerin, Tafluprost