Bimatoprost

drug
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Also known as AGN 192024AGN-192024Bimatoprost component of ganfortDurystaLatisseLumiganProstamideUS9271961

Summary

Bimatoprost (CHEMBL1200963) is an approved small-molecule antiglaucoma drug (ATC S01EE03) targeting PTGFR; indicated across 10 conditions including open-angle glaucoma and ocular hypertension.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: S01EE03
  • Targets: 1 (PTGFR)
  • Indications: 10 conditions
  • Clinical trials: 98
  • Chemistry: 415.6 Da · C25H37NO4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1200963
NameBimatoprost
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID5311027
ChEBICHEBI:51230
ATCS01EE03
Molecular formulaC25H37NO4
Molecular weight415.6
InChIKeyAQOKCDNYWBIDND-FTOWTWDKSA-N

SMILES: CCNC(=O)CCC/C=C\C[C@H]1[C@H](C[C@H]([C@@H]1/C=C/[C@H](CCC2=CC=CC=C2)O)O)O

IUPAC name: (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3S)-3-hydroxy-5-phenylpent-1-enyl]cyclopentyl]-N-ethylhept-5-enamide

Pharmacological roles (ChEBI): antiglaucoma drug, antihypertensive agent.

Also known as: AGN 192024, AGN-192024, Bimatoprost, Bimatoprost component of ganfort, Durysta, Latisse, Lumigan, Prostamide, BIMATOPROST, bimatoprost, US9271961

Patent coverage: 2,523 distinct patent families (11,007 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).

GeneTargetActionpAffinityCancer dependencyUniProt
PTGFRFP receptorFull agonist5.30%P43088

Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Aldo-keto reductase family 1 member C3, Bile salt export pump.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
AKR1C35.3IC505000nMCHEMBL_ACT_17758231

Target pathways

Aggregated over 1 target gene(s): PTGFR.

Top Reactome pathways

2 total, by targets touching each:

PathwayTargetsGenes
Prostanoid ligand receptors1PTGFR
G alpha (q) signalling events1PTGFR

Dominant GO biological processes

GO termTargets
inflammatory response1
G protein-coupled receptor signaling pathway1
adenylate cyclase-activating G protein-coupled receptor signaling pathway1
positive regulation of cytosolic calcium ion concentration1
parturition1
positive regulation of cell population proliferation1
positive regulation of gene expression1
response to estradiol1
response to lipopolysaccharide1
negative regulation of apoptotic process1
cellular response to prostaglandin D stimulus1
signal transduction1
response to lipid1

Indications & clinical

Indications

10 indications (5 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).

IndicationTrial phaseMONDOEFO
open-angle glaucoma4MONDO:0005338EFO:0004190
ocular hypertension4MONDO:0006875EFO:1001069
hypotrichosis4MONDO:0003037MONDO:0003037
glaucoma4MONDO:0005041MONDO:0005041
androgenetic alopecia2MONDO:0005339EFO:0004191
alopecia2MONDO:0004907MONDO:0004907
alopecia areata1MONDO:0005340EFO:0004192
vitiligo0MONDO:0008661EFO:0004208

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 98.

Phase distribution

PhaseTrials
PHASE439
PHASE321
Not specified14
PHASE213
PHASE1/PHASE24
PHASE13
EARLY_PHASE13
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06761313PHASE4ACTIVE_NOT_RECRUITINGTriplenex (triple Fixed Combination) Use Evaluation in Patients with Glaucoma
NCT07217678PHASE4RECRUITINGBiomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensive Medication Use
NCT00273455PHASE4COMPLETEDLumigan Versus Cosopt
NCT00347802PHASE4COMPLETEDDiurnal Curves With Bimatoprost 0.03% Versus Travoprost 0.004%
NCT00347841PHASE4COMPLETEDEfficacy of Bimatoprost 0.03% in Patients Who Are Low-Responders to Latanoprost
NCT00348023PHASE4COMPLETEDBimatoprost Monotherapy vs. Dual Therapy With Travoprost and Timolol in Patients With Glaucoma and Ocular Hypertension
NCT00348062PHASE4COMPLETEDA Multicenter Evaluation of Methods to Reduce Hyperemia Associated With Bimatoprost Therapy for Glaucoma or Ocular Hypertension
NCT00355446PHASE4COMPLETEDBioavailability of Bimatoprost Ophthalmic Solution in Human Aqueous.
NCT00440011PHASE4COMPLETEDBimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost 0.005%
NCT00486486PHASE4COMPLETED24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination
NCT00539526PHASE4COMPLETEDEvaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues
NCT00541242PHASE4COMPLETEDSafety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With Glaucoma or Ocular Hypertension
NCT00705757PHASE4COMPLETEDThe Effects of Xalatan, Travatan and Lumigan on Skin Pigmentation Near the Eye
NCT00847483PHASE4COMPLETEDComparison of Latanoprost With Travoprost and Bimatoprost in Patients With Elevated IOP. A 12-weeks, Masked Evaluator, Phase IV Multi-center Study in the US
NCT01170884PHASE4COMPLETEDComparing Safety and Efficacy of Combigan® and Lumigan® With Lumigan® Alone in Glaucoma or Ocular Hypertension Subjects Treated With Xalatan®
NCT01202513PHASE4WITHDRAWNTopical Bimatoprost Solution 0.03%in Stable Vitiligo
NCT01229423PHASE4COMPLETEDSafety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subjects
NCT01243567PHASE4COMPLETEDSafety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost in Patients With Open-Angle Glaucoma Who Have Never Been Treated
NCT01271686PHASE4COMPLETED24-hour IOP-lowering Effect of 0.01% Bimatoprost
NCT01298700PHASE4COMPLETEDLong-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension
NCT01387906PHASE4COMPLETEDLatisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: Latisse Versus Placebo
NCT01448837PHASE4COMPLETED24-Hour Intraocular Pressure Control With Bimatoprost/Timolol Versus Latanoprost as First Choice
NCT01464424PHASE4COMPLETEDAssessment of Intraocular Pressure (IOP) Control in Subjects With Open-Angle Glaucoma or Ocular Hypertension Treated With Travoprost 0.004% (TRAVATAN® Z) or Bimatoprost 0.01% (LUMIGAN®)
NCT01594970PHASE4COMPLETEDA Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma (POAG) or Ocular Hypertension (OH)
NCT01655758PHASE4COMPLETED24-hour Control of Intraocular Pressure (IOP) in Ocular Hypertension
NCT01664039PHASE4COMPLETEDAn Efficacy and Tolerability Study of TRAVATAN® Versus LUMIGAN®
NCT01833741PHASE4COMPLETEDA Study of LUMIGAN® RC in the Clinical Setting
NCT01881126PHASE4COMPLETEDAn Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0.004% and Timolol 0.5% in Subjects With Glaucoma or Ocular Hypertension
NCT01975714PHASE4COMPLETEDIntraocular Pressure and Tolerability Study of Preservative-free Prostaglandins (Bimatoprost and Latanoprost) on Glaucoma and Ocular Hypertension: European, Multicentric, Investigator-led, Single Masked Study
NCT01978015PHASE4COMPLETEDBlood-aqueous Barrier Changes After the Use of Timolol and Prostaglandin Analogues Fixed Combination in Pseudophakic Patients With POAG
NCT02017327PHASE4COMPLETEDSafety and Efficacy Assessment of Monoprost® in Comparison With Lumigan® 0.01 % and Lumigan® 0.03% Unit Dose
NCT02020512PHASE4COMPLETEDA Study of 0.03% Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocular Hypertension
NCT02059655PHASE4COMPLETEDProstaglandin F2-alpha Eye Drops in Thyroid Eye Disease (Bima Study)
NCT02061683PHASE4COMPLETEDA Study of Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocular Hypertension
NCT02097719PHASE4COMPLETEDEfficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0.004% and Timolol 0.5% in Subjects With Glaucoma or Ocular Hypertension
NCT02571712PHASE4COMPLETEDSafety of GANFORT® Ophthalmic Solution in Chinese Patients With Open-angle Glaucoma or Ocular Hypertension
NCT03487042PHASE4UNKNOWNBimatoprost 0.03% Solution With NB-UVB Versus Their Use With Fractional Carbon Dioxide Laser in Treatment of Generalized Vitiligo
NCT03966560PHASE4COMPLETEDChoroidal Thickness and Its Correlations With Ocular Parameters in Primary Open-angle Glaucoma
NCT04981886PHASE4UNKNOWNIntraocular Pressure Reduction Efficacy of Rhopressa and Lumigan in Normal Tension Glaucoma
NCT00300443PHASE2/PHASE3COMPLETEDSafety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hypertension

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 0 clinical and 1 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

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:

MoleculeSourceStatusShared targets
DINOPROSTChEMBL + PubChemPhase 4 (approved)PTGFR
DINOPROSTONEChEMBL + PubChemPhase 4 (approved)PTGFR
LAROPIPRANTChEMBLPhase 4 (approved)PTGFR
SEPETAPROSTChEMBLPhase 3PTGFR
CLOPROSTENOLChEMBL + PubChemPhase 2 (approved)PTGFR
EBOPIPRANTChEMBLPhase 2PTGFR
FLUPROSTENOLChEMBLPhase 2PTGFR
BelzutifanPubChemApprovedPTGFR
GrapiprantPubChemApprovedPTGFR
LatanoprostPubChemApprovedPTGFR
Latanoprostene BunodPubChemApprovedPTGFR
NitroglycerinPubChemApprovedPTGFR
TafluprostPubChemApprovedPTGFR