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The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at The data is made available under the Creative Commons License (CC BY 3.0, For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

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Accession:CHEBI:116315 term browser browse the term
Definition:A member of the class of azabicycloalkanes that is 1,3-diazabicyclo[2.2.0]hex-4-en-2-one substituted at position 6 by a 5-amino-5-methyl-2,4-dioxodihydropyrimidin-6-yl group.
Synonyms:exact_synonym: 5-amino-5-methyl-6-(2-oxo-1,3-diazabicyclo[2.2.0]hex-4-en-6-yl)dihydropyrimidine-2,4(1H,H)-dione
 related_synonym: Formula=C9H11N5O3;   InChI=1S/C9H11N5O3/c1-9(10)5(12-7(16)13-6(9)15)3-2-4-11-8(17)14(3)4/h2-3,5H,10H2,1H3,(H,11,17)(H2,12,13,15,16);   InChIKey=JJFGFASKBCXOBF-UHFFFAOYSA-N;   SMILES=N1C(NC(C(C1C2N3C(NC3=C2)=O)(C)N)=O)=O
 xref: PMID:22817898

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Path 1
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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            prokaryotic metabolite 0
              bacterial metabolite 0
                Mycoplasma genitalium metabolite 0
                  5-amino-5-methyl-6-\{2-oxo-1,3-diazabicyclo[2.2.0]hex-4-en-6-yl\}-1,3-diazinane-2,4-dione 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    main group molecular entity 0
                      s-block molecular entity 0
                        hydrogen molecular entity 0
                          hydrides 0
                            inorganic hydride 0
                              pnictogen hydride 0
                                nitrogen hydride 0
                                  azane 0
                                    ammonia 0
                                      organic amino compound 0
                                        aromatic amine 0
                                          aminopyrimidine 0
                                            5-amino-5-methyl-6-\{2-oxo-1,3-diazabicyclo[2.2.0]hex-4-en-6-yl\}-1,3-diazinane-2,4-dione 0
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