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Atomfair 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one 1H-ODQ C9H5N3O2

Description 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (CAS No. 443-82-3) is a heterocyclic organic compound with the molecular formula C9H5N3O2. This high-purity chemical is widely utilized in pharmacological and biochemical research due to its role as a selective inhibitor of soluble guanylyl cyclase (sGC). It is supplied as a crystalline solid with >98% purity, verified by HPLC and NMR analysis. Ideal for researchers studying nitric oxide signaling pathways, this compound is packaged under inert conditions to ensure stability and longevity. Store at -20??C in a dry environment to maintain optimal quality.

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Description

Description

1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (CAS No. 443-82-3) is a heterocyclic organic compound with the molecular formula C9H5N3O2. This high-purity chemical is widely utilized in pharmacological and biochemical research due to its role as a selective inhibitor of soluble guanylyl cyclase (sGC). It is supplied as a crystalline solid with >98% purity, verified by HPLC and NMR analysis. Ideal for researchers studying nitric oxide signaling pathways, this compound is packaged under inert conditions to ensure stability and longevity. Store at -20??C in a dry environment to maintain optimal quality.

  • CAS No: 443-82-3
  • Molecular Formula: C9H5N3O2
  • Molecular Weight: 187.15
  • Exact Mass: 187.038176411
  • Monoisotopic Mass: 187.038176411
  • IUPAC Name: [1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one
  • SMILES: C1=CC=C2C(=C1)N=CC3=NOC(=O)N23
  • Synonyms: 41443-28-1, 1h-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one, 1H-ODQ, 1H-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one, DTXSID2036796

Application

1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one is primarily used as a potent and selective inhibitor of soluble guanylyl cyclase (sGC), making it valuable in studies of nitric oxide-mediated signaling pathways. Researchers employ this compound to investigate cardiovascular and neurological systems where sGC plays a critical role. Its application extends to in vitro and ex vivo experiments aimed at elucidating the mechanisms of vasodilation and platelet aggregation.

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