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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:acedapsone
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Accession:CHEBI:139474 term browser browse the term
Definition:A sulfone that is dapsone in which both of the amino groups been acetylation. An antimicrobial drug, it also has antimalarial activity.
Synonyms:exact_synonym: N,N'-[sulfonyldi(4,1-phenylene)]diacetamide
 related_synonym: 4',4'''-sulfonylbis(acetanilide);   Formula=C16H16N2O4S;   InChI=1S/C16H16N2O4S/c1-11(19)17-13-3-7-15(8-4-13)23(21,22)16-9-5-14(6-10-16)18-12(2)20/h3-10H,1-2H3,(H,17,19)(H,18,20);   InChIKey=AMTPYFGPPVFBBI-UHFFFAOYSA-N;   N,N'-(sulfonyldi-4,1-phenylene)bisacetamide;   SMILES=S(=O)(=O)(C1=CC=C(C=C1)NC(C)=O)C2=CC=C(C=C2)NC(C)=O;   acedapsona;   acedapsonum
 alt_id: CHEBI:135417
 xref: CAS:77-46-3;   PMID:29045131;   PMID:3543161;   PMID:3794408;   PMID:4793795;   PMID:6991817;   Reaxys:2164071;   Wikipedia:Acedapsone


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        antimicrobial agent 0
          antimicrobial drug 0
            acedapsone 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
                                        primary amino compound 0
                                          primary amine 0
                                            primary arylamine 0
                                              aniline 0
                                                anilide 0
                                                  acedapsone 0
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