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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:hydroxybenzyl alcohol
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Accession:CHEBI:24679 term browser browse the term
Definition:Any member of the class of benzyl alcohols that is a benzyl alcohol substituted by at least one hydroxy group on the benzene ring.
Synonyms:related_synonym: hydroxybenzyl alcohols



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salicin term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Alb albumin multiple interactions ISO ALB protein binds to and affects the transport of salicin CTD PMID:8831264 NCBI chr14:17,607,397...17,622,814
Ensembl chr14:17,607,381...17,622,836
JBrowse link
G Tas2r118 taste receptor, type 2, member 118 multiple interactions
increases activity
ISO 4-((diethylamino)sulfonyl)benzoic acid inhibits the reaction [salicin results in increased activity of TAS2R16 protein]; Probenecid inhibits the reaction [salicin results in increased activity of TAS2R16 protein] CTD PMID:21629661 NCBI chr 4:52,449,208...52,450,107
Ensembl chr 4:52,449,208...52,450,107
JBrowse link
salicyl alcohol term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Alb albumin multiple interactions ISO ALB protein binds to and affects the transport of salicyl alcohol CTD PMID:8831264 NCBI chr14:17,607,397...17,622,814
Ensembl chr14:17,607,381...17,622,836
JBrowse link
G Bche butyrylcholinesterase multiple interactions ISO [2-(2-cresyl)-4H-1-3-2-benzodioxaphosphorin-2-oxide binds to and results in decreased activity of BCHE protein] which results in increased abundance of salicyl alcohol CTD PMID:22898212 NCBI chr 2:158,308,674...158,401,148
Ensembl chr 2:158,307,584...158,401,148
JBrowse link
G Sod2 superoxide dismutase 2 multiple interactions EXP salicyl alcohol inhibits the reaction [2,2'-azobis(2-amidinopropane) results in decreased activity of SOD2 protein] CTD PMID:19665455 NCBI chr 1:47,638,318...47,645,163
Ensembl chr 1:47,636,528...47,645,189
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19740
    chemical entity 19738
      molecular entity 19738
        polyatomic entity 19698
          heteroatomic molecular entity 19650
            hydroxides 19255
              organic hydroxy compound 18867
                phenols 18567
                  hydroxybenzyl alcohol 4
                    3-hydroxybenzyl alcohol 0
                    dihydropyriculariol 0
                    salicyl alcohol + 4
                    trichoxide 0
                    virensol A 0
                    virensol B 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19740
    subatomic particle 19738
      composite particle 19738
        hadron 19738
          baryon 19738
            nucleon 19738
              atomic nucleus 19738
                atom 19738
                  main group element atom 19686
                    p-block element atom 19686
                      chalcogen 19482
                        oxygen atom 19459
                          oxygen molecular entity 19459
                            hydroxides 19255
                              organic hydroxy compound 18867
                                alcohol 15178
                                  aromatic alcohol 450
                                    benzyl alcohols 409
                                      hydroxybenzyl alcohol 4
                                        3-hydroxybenzyl alcohol 0
                                        dihydropyriculariol 0
                                        salicyl alcohol + 4
                                        trichoxide 0
                                        virensol A 0
                                        virensol B 0
paths to the root