CAS 402473-54-5|ONO-AE3-208

Introduction:Basic information about CAS 402473-54-5|ONO-AE3-208, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameONO-AE3-208
CAS Number402473-54-5Molecular Weight404.434
Density1.3±0.1 g/cm3Boiling Point662.4±55.0 °C at 760 mmHg
Molecular FormulaC24H21FN2O3Melting Point/
MSDS/Flash Point354.4±31.5 °C

Names

Name4-[4-cyano-2-[2-(4-fluoronaphthalen-1-yl)propanoylamino]phenyl]butanoic acid
SynonymMore Synonyms

ONO-AE3-208 BiologicalActivity

DescriptionONO-AE3-208 is an EP4 antagonist, and suppresses cell invasion, migration, and metastasis of prostate cancer.
Related CatalogSignaling Pathways >>GPCR/G Protein >>Prostaglandin ReceptorResearch Areas >>Cancer
Target

EP4

In VitroONO-AE3-208 surpresses the in vitro cell invasion and migration in a dose-dependent manner without affecting cell proliferation[1]. ONO-AE3-208 abolisheS CTGF in the presence of the EET synthesis inhibitor MS-PPOH. Arachidonic acid (AA) causeS dose-dependent dilation of the attached Af-Art, and this effect is blocked by ONO-AE3-208[2].
In VivoONO-AE3-208 surpresses the in vivo bone metastasis of PC3 cells in mice[1]. The photon tumor burdens are significantly increased in a time-dependent manner in the control group in comparison with those in the ONO-AE3-208-treated group. The rate of metastasis formation is significantly higher in the former than in the latter. The median time of metastasis formation is 29 d in the ONO-AE3-208-treated animals as compared with 21 d in the controls[3].
References

[1]. Xu S, et al. An EP4 Antagonist ONO-AE3-208 Suppresses Cell Invasion, Migration, and Metastasis of Prostate Cancer. Cell Biochem Biophys. 2014 Apr 18.

[2]. Ren Y, et al. Prostaglandin E2 mediates connecting tubule glomerular feedback. Hypertension. 2013 Dec;62(6):1123-8.

[3]. Xu S, et al. Inhibitory effect of ONO-AE3-208 on the formation of bone metastasis of prostate cancer in mice. Zhonghua Nan Ke Xue. 2014 Aug;20(8):684-9.

[4]. Thieme K, et al. EP4 inhibition attenuates the development of diabetic and non-diabetic experimental kidney disease. Sci Rep. 2017 Jun 13;7(1):3442.

Chemical & Physical Properties

Density1.3±0.1 g/cm3
Boiling Point662.4±55.0 °C at 760 mmHg
Molecular FormulaC24H21FN2O3
Molecular Weight404.434
Flash Point354.4±31.5 °C
Exact Mass404.153625
PSA90.19000
LogP4.56
Vapour Pressure0.0±2.1 mmHg at 25°C
Index of Refraction1.637
InChIKeyMTDIMKNAJUQTIO-UHFFFAOYSA-N
SMILESCC(C(=O)Nc1cc(C#N)ccc1CCCC(=O)O)c1ccc(F)c2ccccc12
Storage condition2-8℃

Synonyms

4-Cyano-2-[[2-(4-fluoro-1-naphthalenyl)-1-oxopropyl]amino]benzenebutanoic acid
ONO AE3 208
4-[4-cyano-2-[2-(4-fluoro-1-naphthyl)propanoylamino]phenyl]butanoic acid
4-(4-cyano-2-(2-(4-fluoronaphthalen-1-yl)propionylamino)phenyl)butyric acid
ONO-AE3-208||ONO AE3 208
4-(4-Cyano-2-{[2-(4-fluoro-1-naphthyl)propanoyl]amino}phenyl)butanoic acid
Benzenebutanoic acid, 4-cyano-2-[[2-(4-fluoro-1-naphthalenyl)-1-oxopropyl]amino]-
ONO-AE3-208
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