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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:76277 term browser browse the term
Definition:A hydroxamic acid obtained by formal condensation of the carboxy group of 3-[5-(4-chlorophenyl)-1-(4-methoxyphenyl)pyrazol-3-yl]propanoic acid with the amino group of N-methylhydroxylamine. It is used in veterinary medicine for the control of pain and inflammation caused by musculoskeletal disorders such as hip dysplasia and arthritis in dogs.
Synonyms:exact_synonym: 3-[5-(4-chlorophenyl)-1-(4-methoxyphenyl)-1H-pyrazol-3-yl]-N-hydroxy-N-methylpropanamide
 related_synonym: 5-(p-Chlorophenyl)-1-(p-methoxyphenyl)-N-methylpyrazole-3-propionohydroxamic acid;   Formula=C20H20ClN3O3;   InChI=1S/C20H20ClN3O3/c1-23(26)20(25)12-7-16-13-19(14-3-5-15(21)6-4-14)24(22-16)17-8-10-18(27-2)11-9-17/h3-6,8-11,13,26H,7,12H2,1-2H3;   InChIKey=XYKWNRUXCOIMFZ-UHFFFAOYSA-N;   ORF 20485;   RWJ 20485;   SMILES=COc1ccc(cc1)-n1nc(CCC(=O)N(C)O)cc1-c1ccc(Cl)cc1;   Zubrin;   tepoxalina;   tepoxaline;   tepoxaliume
 xref: CAS:103475-41-8;   KEGG:C18362;   KEGG:D06075
 xref_mesh: MESH:C073135
 xref: PMID:16343292;   PMID:19161461;   PMID:19175721;   PMID:19552701;   PMID:19566476;   PMID:19624842;   PMID:20000343;   PMID:20807147;   PMID:21036634;   PMID:21062309;   PMID:21348304;   PMID:21497474;   PMID:21565533;   PMID:21569197;   PMID:21962280;   PMID:22091562;   PMID:22240988;   PMID:22287649;   PMID:22726277;   PMID:22986275;   PMID:23349526;   PMID:23718664;   PMID:23802664;   PMID:7652766;   PMID:9703407;   Patent:WO2007022427;   Reaxys:4334297;   VSDB:1877;   Wikipedia:Tepoxalin

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tepoxalin term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Alox5 arachidonate 5-lipoxygenase decreases activity
multiple interactions
tepoxalin results in decreased activity of ALOX5 protein
[tepoxalin results in decreased activity of ALOX5 protein] inhibits the reaction [Indomethacin results in increased abundance of Leukotriene B4]
CTD PMID:9223651 PMID:12629151 NCBI chr 4:149,531,329...149,578,696
Ensembl chr 4:149,531,515...149,578,743
JBrowse link
G Icam1 intercellular adhesion molecule 1 multiple interactions ISO tepoxalin inhibits the reaction [Lipopolysaccharides results in increased expression of ICAM1 mRNA] CTD PMID:8566054 NCBI chr 8:19,553,063...19,565,438
Ensembl chr 8:19,553,645...19,565,438
JBrowse link
G Il6 interleukin 6 multiple interactions ISO tepoxalin inhibits the reaction [Tetradecanoylphorbol Acetate results in increased expression of IL6 mRNA] CTD PMID:7759567 NCBI chr 4:5,214,602...5,219,178
Ensembl chr 4:5,213,394...5,219,178
JBrowse link
G Itgam integrin subunit alpha M multiple interactions ISO tepoxalin inhibits the reaction [Lipopolysaccharides results in increased expression of ITGAM protein] CTD PMID:8566054 NCBI chr 1:182,659,047...182,709,495
Ensembl chr 1:182,659,000...182,709,503
JBrowse link
G Sele selectin E multiple interactions ISO tepoxalin inhibits the reaction [Lipopolysaccharides results in increased expression of SELE mRNA] CTD PMID:8566054 NCBI chr13:76,402,841...76,412,741
Ensembl chr13:76,403,304...76,412,741
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19812
    role 19763
      biological role 19763
        immunomodulator 14913
          tepoxalin 5
Path 2
Term Annotations click to browse term
  CHEBI ontology 19812
    subatomic particle 19811
      composite particle 19811
        hadron 19811
          baryon 19811
            nucleon 19811
              atomic nucleus 19811
                atom 19811
                  main group element atom 19710
                    p-block element atom 19710
                      carbon group element atom 19631
                        carbon atom 19621
                          organic molecular entity 19621
                            organic group 18730
                              organic divalent group 18721
                                organodiyl group 18721
                                  carbonyl group 18670
                                    carbonyl compound 18670
                                      carboxylic acid 18367
                                        carboacyl group 17487
                                          univalent carboacyl group 17487
                                            carbamoyl group 17303
                                              carboxamide 17303
                                                hydroxamic acid 6288
                                                  tepoxalin 5
paths to the root