Date published: 2025-9-14

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CAY10449

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Application:
CAY10449 is antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner. Likewise, it inhibits the binding of tritiated iloprost to rodent neuroblastoma cells with a Ki of about 3 nM.
Molecular Weight:
323.39
Molecular Formula:
C19H21N3O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Potent compounds with high-affinity ligands and functional antagonists for the human IP (prostacyclin) receptor.1 Antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner. Likewise, it inhibits the binding of tritiated iloprost to rodent neuroblastoma cells with a Ki of about 3 nM.1


CAY10449 References

1 Clark, R.D., Jahangir, A., Severance, D., et al. Discovery and SAR development of 2-(phenylamino) imidazolines as prostacyclin receptor antagonists. Bioorg Medicinal Chem Letters 14 1053-1056 (2004).

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

CAY10449, 1 mg

sc-223863
1 mg
$92.00

CAY10449, 5 mg

sc-223863A
5 mg
$311.00