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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:Chloramphenicol succinate
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Accession:CHEBI:3606 term browser browse the term
Synonyms:related_synonym: Formula=C15H16Cl2N2O8;   InChI=1S/C15H16Cl2N2O8/c16-14(17)15(24)18-10(7-27-12(22)6-5-11(20)21)13(23)8-1-3-9(4-2-8)19(25)26/h1-4,10,13-14,23H,5-7H2,(H,18,24)(H,20,21)/t10-,13-/m1/s1;   InChIKey=LIRCDOVJWUGTMW-ZWNOBZJWSA-N;   SMILES=C1([C@H]([C@](NC(C(Cl)Cl)=O)(COC(=O)CCC(O)=O)[H])O)=CC=C([N+](=O)[O-])C=C1;   chloramphenicol monosuccinate sodium salt;   levomycetin sodium succinate;   sodium chloramphenicol succinate
 xref: CAS:3544-94-3;   Drug_Central:4653;   KEGG:C11727;   KEGG:C13962;   KEGG:D02185;   KEGG:D07675;   PDBeChem:CL8


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19875
    role 19825
      application 19494
        refrigerant 17511
          ammonia 17039
            organic amino compound 17038
              amine 7792
                amphetamines 5720
                  Chloramphenicol succinate 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19875
    subatomic particle 19873
      composite particle 19873
        hadron 19873
          baryon 19873
            nucleon 19873
              atomic nucleus 19873
                atom 19873
                  main group element atom 19763
                    p-block element atom 19763
                      carbon group element atom 19668
                        carbon atom 19657
                          organic molecular entity 19657
                            organic group 18569
                              organic divalent group 18560
                                organodiyl group 18560
                                  carbonyl group 18468
                                    carbonyl compound 18468
                                      dicarboxylic acids and O-substituted derivatives 10300
                                        dicarboxylic acid 10292
                                          alpha,omega-dicarboxylic acid 2784
                                            succinic acid 220
                                              succinate ester 111
                                                hemisuccinate 107
                                                  Chloramphenicol succinate 0
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