ONO-AE3-208
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


ONO-AE3-208
Description:
ONO-AE3-208 is a selective and orally active EP4 receptor antagonist with a Ki of 1.3 nM. ONO-AE3-208 shows less potently affects EP3, FP, and TP receptors (Ki of 30 nM, 790 nM, and 2400 nM, respectively) . ONO-AE3-208 suppresses cell invasion, migration, and metastasis of prostate cancer[1][2].Product Name Alternative:
AE 3-208UNSPSC:
12352005Hazard Statement:
H302, H315, H319, H335Target:
Prostaglandin ReceptorType:
Reference compoundRelated Pathways:
GPCR/G ProteinApplications:
Cancer-programmed cell deathField of Research:
Cancer; EndocrinologyAssay Protocol:
https://www.medchemexpress.com/ONO-AE3-208.htmlConcentration:
10mMPurity:
98.65Solubility:
DMSO : 33.33 mg/mL (ultrasonic)Smiles:
N#CC1=CC=C (C (NC (C (C2=C3C=CC=CC3=C (F) C=C2) C) =O) =C1) CCCC (O) =OMolecular Formula:
C24H21FN2O3Molecular Weight:
404.43Precautions:
H302, H315, H319, H335References & Citations:
[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.|[5]Kenji Kabashima, et al. The prostaglandin receptor EP4 suppresses colitis, mucosal damage and CD4 cell activation in the gut. J Clin Invest. 2002 Apr;109 (7) :883-93.Shipping Conditions:
Room TemperatureStorage Conditions:
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category:
Reference compound1Clinical Information:
No Development ReportedIsoform:
EP; FP; TXA2/TPCAS Number:
402473-54-5
