CHEBI:133247 - N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide

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ChEBI Name N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide
ChEBI ID CHEBI:133247
ChEBI ASCII Name N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide
Definition A nitrone that is the N-oxido derivative of N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Sabrina Toro
Supplier Information
Download Molfile XML SDF
Formula C12H19N3O
Net Charge 0
Average Mass 221.299
Monoisotopic Mass 221.15281
InChI InChI=1S/C12H19N3O/c1-8-9(2)14-11(10(3)13-8)7-15(16)12(4,5)6/h7H,1-6H3
InChIKey BESRYENXPUCIID-UHFFFAOYSA-N
SMILES C=1(C(=NC(=C(N1)C)C)C(=[N+]([O-])C(C)(C)C)[H])C
Roles Classification
Application(s): platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
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ChEBI Ontology
Outgoing N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide (CHEBI:133247) has role neuroprotective agent (CHEBI:63726)
N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide (CHEBI:133247) has role platelet aggregation inhibitor (CHEBI:50427)
N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide (CHEBI:133247) is a nitrone (CHEBI:77477)
N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide (CHEBI:133247) is a pyrazines (CHEBI:38314)
IUPAC Name
N-tert-butyl(3,5,6-trimethylpyrazin-2-yl)methanimine N-oxide
Synonyms Sources
2-[[(1,1-Dimethylethyl)oxidoimino]-methyl]-3,5,6-tri-methylpyrazine ChEBI
TBN
Note: (2017-11-20) Ambiguous - TBN has been used as an abbreviation for t-butyl nitrite; triple block nanocarrier; and traumatic biliary neuroma among others.
 ChEBI
Registry Numbers Types Sources
1083171-75-8 CAS Registry Number Reaxys
18904586 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21243778 PubMed citation Europe PMC
24305623 PubMed citation Europe PMC
27452038 PubMed citation Europe PMC
27841332 PubMed citation Europe PMC
28160291 PubMed citation Europe PMC
28342896 PubMed citation Europe PMC
Last Modified
20 November 2017