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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/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.
Term:xibenolol
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Accession:CHEBI:135026 term browser browse the term
Synonyms:related_synonym: Formula=C15H25NO2;   InChI=1S/C15H25NO2/c1-11-7-6-8-14(12(11)2)18-10-13(17)9-16-15(3,4)5/h6-8,13,16-17H,9-10H2,1-5H3;   InChIKey=RKUQLAPSGZJLGP-UHFFFAOYSA-N;   SMILES=O(CC(CNC(C)(C)C)O)C1=C(C)C(C)=CC=C1
 xref: CAS:30187-90-7;   Drug_Central:3657
 xref_mesh: MESH:C006027


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19808
    chemical entity 19806
      group 19765
        polyatomic entity 19764
          molecule 19670
            organic molecule 19655
              organic cyclic compound 19468
                organic aromatic compound 19336
                  aromatic ether 16509
                    xibenolol 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19808
    subatomic particle 19806
      composite particle 19806
        hadron 19806
          baryon 19806
            nucleon 19806
              atomic nucleus 19806
                atom 19806
                  main group element atom 19756
                    main group molecular entity 19756
                      p-block molecular entity 19756
                        carbon group molecular entity 19705
                          organic molecular entity 19702
                            heteroorganic entity 19460
                              organochalcogen compound 19224
                                organooxygen compound 19141
                                  ether 17259
                                    aromatic ether 16509
                                      xibenolol 0
paths to the root