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Aromatic organic heterocyclic compounds that consist of a five-membered ring with four carbon atoms and one nitrogen atom that forms an amine functional group.
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17-Phenyl trinor PGF2α isopropyl ester is a synthetic prostaglandin F2α analogue used as a research reagent for prostaglandin receptor and endocrinology studies (CAS 130209-76-6). It is provided in small milligram quantities for analytical and biological experiments and is typically supplied with characterization data.
Synthetic prostaglandin F2α analogue suitable for receptor studies.
High purity, commonly reported as ≥98% by some suppliers.
Available in small milligram pack sizes for research applications.
Soluble in common organic solvents; consult supplier documentation for solvent guidance.
Useful as a reference standard for pharmacology and assay validation.
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17-phenyl trinor prostaglandin F2α isopropyl ester (CAS 130209-76-6) is a synthetic F-series prostaglandin analog and FP receptor agonist used in biomedical research. It is supplied as a small, premeasured solid for laboratory studies of prostaglandin signaling and ocular hypotensive activity.
Prostaglandin F2α analog with activity at FP receptors.
Suitable for in vitro and in vivo research applications.
Available as a 50 MG premeasured solid for laboratory use.
CAS 130209-76-6 provided for unambiguous identification.
Molecular formula C26H38O5; molecular weight 430.6 g/mol.
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Isopropyl ester derivative of 17-phenyl trinor prostaglandin F2α used as a research reagent in prostaglandin pharmacology. The compound acts as a potent FP receptor agonist and is supplied at high purity for in vitro and pharmacological studies.
Isopropyl ester of 17-phenyl trinor PGF2α.
Potent FP receptor agonist for prostaglandin research.
High purity (≥98%).
Molecular weight 430.6 g/mol; formula C26H38O5.
Available in small research pack sizes such as 5 mg.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
JMS-17-2 is a potent, selective antagonist of the chemokine receptor CX3CR1 used in research to inhibit CX3CR1-mediated signaling. It shows an IC50 of 0.32 nM and has been reported to impair metastatic seeding and colonization of breast cancer cells, making it useful for in vitro pharmacology and cell-based assays.
Potent CX3CR1 inhibition (IC50 0.32 nM).
High reported purity (99.18%).
Defined chemical characteristics: C25H26ClN3O, MW 419.95 g/mol.
Solid, white to off-white appearance.
Storage: in solvent, -80 °C up to 6 months; -20 °C up to 1 month; protect from light.
Relevant for studies of metastatic seeding and colonization in cancer research.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More