1. GPCR/G Protein
  2. Prostaglandin Receptor
  3. Rivenprost

Rivenprost  (Synonyms: ONO-4819; ONO-AE1-734)

Cat. No.: HY-114974 Pureza: 99.0%
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Rivenprost (ONO-4819; ONO-AE1-734) is a selective agonist for prostaglandin E receptor EP4 with Ki of 0.7 nM. Rivenprost exhibits hepatoprotective and bone anabolic effects.

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Rivenprost

Rivenprost Estructura química

No. CAS : 256382-08-8

Tamaño Precio Stock Cantidad
Solvent
100 μg (2.22 mM * 100 μL in Methyl acetate) En stock
Solvent
500 μg (2.22 mM * 500 μL in Methyl acetate) En stock
Solvent
1 mg (2.22 mM * 1 mL in Methyl acetate) En stock

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Descripciòn

Rivenprost (ONO-4819; ONO-AE1-734) is a selective agonist for prostaglandin E receptor EP4 with Ki of 0.7 nM. Rivenprost exhibits hepatoprotective and bone anabolic effects[1][2].

IC50 & Target

EP4

0.7 nM (Ki)

Cellular Effect
Cell Line Type Value Description References
CHO EC50
1.6 nM
Compound: 52, ONO-4819
Agonist activity at mouse EP4 receptor expressed in CHO cells assessed as cAMP production
Agonist activity at mouse EP4 receptor expressed in CHO cells assessed as cAMP production
[PMID: 20218623]
In Vitro

Rivenprost (1 nM–1 μM) stimulates the osteoblast differentiation through upregulation of Runx2 and Osterix, leading to increased bone formation[1].
Rivenprost (1 nM–1 μM) inhibits the adipocytes differentation in bone by downregulating the mRNA expression of PPARγ[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

RT-PCR[1]

Cell Line: C3H10T1/2
Concentration: 1 nM–1 μM
Incubation Time: 7 days
Result: Reduced PPARγ in a dose-dependent manner.
In Vivo

Rivenprost (10 μg/kg, s.c. for 5 weeks) increases bone formation and decreases levels of age-dependent adipocytes in Sprague-Dawley rats[1].
Rivenprost (0.2 mg/kg, i.p., single dosage) exhibits hepatoprotective efficacy towards GalN-/LPS-induced liver injury in wistar rats through inflammatory cytokines such as TNF-α[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague Dawley rats[1]
Dosage: 10 μg/kg
Administration: s.c., twice a day for 5 weeks
Result: Increased osteoblast number, bone volume, mineral apposition rate and bone formation rate.
Decreased adipocyte number.
Animal Model: GalN/LPS-induced acute liver injury in wistar rats[2]
Dosage: 0.2 mg/kg
Administration: i.p., single dosage
Result: Inhibited development of hepatic necrosis, decreased levels of AST, ALT, TNF-α and IFN-γ.
Ensayo clínico
Peso molecular

450.59

Fòrmula

C24H34O6S

No. CAS
Appearance

Liquid

Color

Colorless to light yellow

SMILES

COCC1=CC=CC(C[C@H](O)/C=C/[C@@H]2[C@H](C(C[C@H]2O)=O)CCSCCCC(OC)=O)=C1

Envío

Room temperature in continental US; may vary elsewhere.

Almacenamiento

Solution, -20°C, 2 years

Pureza y Documentación

Purity: 99.0%

Referencias
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Inquiry Information

Nombre del producto:
Rivenprost
Cat. No.:
HY-114974
Cantidad:
MCE Japan Authorized Agent: