Latanoprost Immunology & Inflammation related agonist

Cat.No.S4709

Latanoprost (Xalatan, PhXA41) is a prostaglandin F2alpha analogue and a prostanoid selective FP receptor agonist with an ocular hypertensive effect. This compound increases uveoscleral outflow and thereby reduces intraocular pressure.
Latanoprost Immunology & Inflammation related agonist Chemical Structure

Chemical Structure

Molecular Weight: 432.59

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 432.59 Formula

C26H40O5

Storage (From the date of receipt) 2 years  -20°C  liquid
CAS No. 130209-82-4 Download SDF Storage of Stock Solutions

Synonyms Xalatan, PhXA41, PHXA-41 Smiles CC(C)OC(=O)CCCC=CCC1C(CC(C1CCC(CCC2=CC=CC=C2)O)O)O

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Mechanism of Action

Targets/IC50/Ki
retinoid X receptor α [2]
PGF-prostanoid receptor [3]
In vitro
Latanoprost functioned as both an indirect activator of AMP-activated protein kinase and a selective retinoid X receptor α (RXRα) antagonist able to selectively antagonise the transcription of a RXRα/peroxisome proliferator-activated receptor γ heterodimer[2]. This compound induced morphological abnormality and viability decline of HCS cells in vitro. It induces cell cycle arrest of HCS cells. This chemical induces abnormal changes of plasma membrane, DNA fragmentation and ultrastructural abnormality of HCS cells. Caspase activation in HCS cells is also activated by this compound treatment. It induces MTP disruption and quantitative changes of mitochondrion-associated pro-apoptotic regulators in HCS cells[1]. This compound is effective in inhibiting adipogenesis, reducing lipogenesis, promoting fatty acid oxidation and enhancing GLUT4 translocation and glucose uptake both in adipocytes and myotubes[2].
In vivo
Latanoprost, a clinical drug for treating primary open-angle glaucoma and intraocular hypertension, effectively ameliorates glucose and lipid disorders in two mouse models of type 2 diabetes. Its treatment improves glucose tolerance. Chronic administration of this compound decreases serum lipids and enhances insulin signalling in white adipose tissue and skeletal muscle. It effectually activates AMPK and regulates glucose and lipid metabolism-relevant genes in diabetic mice[2].
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05333419 Completed
Open Angle Glaucoma|Ocular Hypertension
PolyActiva Pty Ltd
March 4 2022 Phase 1
NCT02622334 Completed
Glaucoma
Hoffmann-La Roche
December 29 2015 Phase 1
NCT00941525 Completed
Open Angle Glaucoma|Ocular Hypertension
Aristotle University Of Thessaloniki
September 2009 Phase 4

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