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RO1138452

Cat. No. M9473

All AbMole products are for research use only, cannot be used for human consumption.

RO1138452 Structure
Synonym:

CAY10441

Size Price Availability Quantity
5mg USD 118 In stock
10mg USD 195 In stock
25mg USD 417 In stock
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Quality Control & Documentation
Biological Activity

RO1138452 is a potent and selective antagonist for both human and rat IP receptors and that is possesses analgesic and anti-inflammatory potential. RO1138452 (10 pM-10 μM) added to cells concurrently with a fixed concentration of Taprostene (1 μM) prevents, in a concentration-dependent manner, the inhibition of CXCL9 and CXCL10 release, with p[A]50 (molar) values of -8.73±0.11 and -8.47±0.16 (p>0.05), respectively. RO1138452 (1-10 mg/kg, i.v.) significantly reduces acetic acid-induced abdominal constrictions. RO1138452 (3-100 mg/kg, p.o.) significantly reduces carrageenan-induced mechanical hyperalgesia and edema formation.

Chemical Information
Molecular Weight 309.41
Formula C19H23N3O
CAS Number 221529-58-4
Solubility (25°C) DMSO ≥ 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ayer LM, et al. J Pharmacol Exp Ther. 4,5-Dihydro-1H-imidazol-2-yl)-[4-(4-isopropoxy-benzyl)-phenyl]-amine (RO1138452) is a selective, pseudo-irreversible orthosteric antagonist at the prostacyclin (IP)-receptor expressed by human airway epithelial cells: IP-receptor-mediated inhibition of CXCL9 and CXCL10 release.

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Keywords: RO1138452, CAY10441 supplier, Prostaglandin Receptor, inhibitors, activators

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