Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:exalamide
go back to main search page
Accession:CHEBI:31585 term browser browse the term
Definition:An arenecarboxamide that is salicylamide in which the phenolic hydroxy group has been converted to the corresponding hexyl ether. It has been used as a topical antifungal agent.
Synonyms:exact_synonym: 2-(hexyloxy)benzamide
 related_synonym: 2-hexyloxybenzamide;   2-n-hexyloxybenzamide;   Formula=C13H19NO2;   HBA;   Hyperan;   InChI=1S/C13H19NO2/c1-2-3-4-7-10-16-12-9-6-5-8-11(12)13(14)15/h5-6,8-9H,2-4,7,10H2,1H3,(H2,14,15);   InChIKey=CKSJXOVLXUMMFF-UHFFFAOYSA-N;   SMILES=CCCCCCOc1ccccc1C(N)=O;   exalamida;   exalamidum;   o-hexyloxybenzamide;   ortho-hexyloxybenzamide
 xref: CAS:53370-90-4 "ChemIDplus";   CAS:53370-90-4 "KEGG DRUG";   Drug_Central:1119 "DrugCentral";   KEGG:D01585;   PMID:6386917 "Europe PMC";   Patent:GB726786;   Reaxys:2645003 "Reaxys"


show annotations for term's descendants       view all columns           Sort by:
 

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        antimicrobial agent 0
          antifungal agent 0
            exalamide 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
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            carbamoyl group 0
                                              carboxamide 0
                                                monocarboxylic acid amide 0
                                                  arenecarboxamide 0
                                                    benzamides 0
                                                      salicylamides 0
                                                        salicylamide 0
                                                          exalamide 0
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.