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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:organic nitrogen anion
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Accession:CHEBI:50335 term browser browse the term
Synonyms:related_synonym: organic nitrogen anions



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chloramine T term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cd86 CD86 molecule increases expression ISO chloramine-T results in increased expression of CD86 protein CTD PMID:19665512 NCBI chr11:64,142,193...64,200,816
Ensembl chr11:64,163,828...64,200,818
JBrowse link
G Gpx1 glutathione peroxidase 1 increases expression EXP chloramine-T results in increased expression of GPX1 protein CTD PMID:24213014 NCBI chr 8:109,026,905...109,028,031
Ensembl chr 8:109,026,905...109,028,024
JBrowse link
G Hmox1 heme oxygenase 1 increases expression ISO chloramine-T results in increased expression of HMOX1 mRNA CTD PMID:26244607 NCBI chr19:13,466,287...13,474,082
Ensembl chr19:13,467,244...13,474,079
JBrowse link
G Icam1 intercellular adhesion molecule 1 increases expression ISO chloramine-T results in increased expression of ICAM1 protein CTD PMID:38360295 NCBI chr 8:19,553,063...19,565,438
Ensembl chr 8:19,553,645...19,565,438
JBrowse link
G Il1b interleukin 1 beta increases expression ISO chloramine-T results in increased expression of IL1B protein CTD PMID:38360295 NCBI chr 3:116,577,005...116,583,386
Ensembl chr 3:116,577,010...116,583,415
JBrowse link
G Kcnh2 potassium voltage-gated channel subfamily H member 2 multiple interactions ISO chloramine-T results in increased oxidation of and results in decreased activity of KCNH2 protein CTD PMID:17624316 NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008
JBrowse link
G Msra methionine sulfoxide reductase A decreases response to substance
multiple interactions
ISO MSRA protein results in decreased susceptibility to chloramine-T
S-methylcysteine promotes the reaction [MSRA protein results in decreased susceptibility to chloramine-T]
CTD PMID:19085252 NCBI chr15:38,363,459...38,677,406
Ensembl chr15:38,351,445...38,676,585
JBrowse link
G Muc1 mucin 1, cell surface associated decreases expression ISO chloramine-T results in decreased expression of MUC1 protein CTD PMID:38360295 NCBI chr 2:174,635,989...174,640,738
Ensembl chr 2:174,635,995...174,640,733
JBrowse link
G Nrgn neurogranin multiple interactions
affects phosphorylation
EXP Dithiothreitol inhibits the reaction [chloramine-T affects the phosphorylation of NRGN protein] CTD PMID:21241739 NCBI chr 8:37,255,462...37,263,659
Ensembl chr 8:37,256,930...37,257,516
JBrowse link
G Prdx1 peroxiredoxin 1 increases expression EXP chloramine-T results in increased expression of PRDX1 protein CTD PMID:24213014 NCBI chr 5:130,147,258...130,162,856
Ensembl chr 5:130,147,204...130,162,856
JBrowse link
G Selp selectin P decreases expression ISO chloramine-T results in decreased expression of SELP protein CTD PMID:11441983 NCBI chr13:76,476,229...76,511,846
Ensembl chr13:76,476,295...76,511,845
JBrowse link
G Sod2 superoxide dismutase 2 increases expression EXP chloramine-T results in increased expression of SOD2 protein CTD PMID:24213014 NCBI chr 1:47,638,318...47,645,163
Ensembl chr 1:47,636,528...47,645,189
JBrowse link
dimenhydrinate term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bche butyrylcholinesterase decreases activity ISO Dimenhydrinate results in decreased activity of BCHE protein CTD PMID:236606 NCBI chr 2:158,308,674...158,401,148
Ensembl chr 2:158,307,584...158,401,148
JBrowse link
G Slc22a2 solute carrier family 22 member 2 multiple interactions ISO Dimenhydrinate inhibits the reaction [SLC22A2 protein results in increased uptake of 4-(4-dimethylaminostyryl)-1-methylpyridinium] CTD PMID:21599003 NCBI chr 1:48,121,061...48,163,268
Ensembl chr 1:48,121,061...48,163,268
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19932
    chemical entity 19930
      molecular entity 19930
        ion 17101
          anion 16648
            organic anion 6850
              organic nitrogen anion 14
                8-chlorotheophylline(1-) + 2
                asulam(1-) + 0
                benzimidazolide 0
                chloro(p-tolylsulfonyl)azanide + 12
                cyanamide(2-) + 0
                dasabuvir(1-) + 0
                flucarbazone(1-) + 0
                fomesafen(1-) + 0
                glymidine(1-) + 0
                imidazolide 0
                rabeprazole(1-) + 0
                sulfacetamide(1-) + 0
                sulfadiazinate + 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19932
    subatomic particle 19930
      composite particle 19930
        hadron 19930
          baryon 19930
            nucleon 19930
              atomic nucleus 19930
                atom 19930
                  main group element atom 19876
                    p-block element atom 19876
                      carbon group element atom 19816
                        carbon atom 19812
                          organic molecular entity 19812
                            organic ion 11451
                              organic anion 6850
                                organic nitrogen anion 14
                                  8-chlorotheophylline(1-) + 2
                                  asulam(1-) + 0
                                  benzimidazolide 0
                                  chloro(p-tolylsulfonyl)azanide + 12
                                  cyanamide(2-) + 0
                                  dasabuvir(1-) + 0
                                  flucarbazone(1-) + 0
                                  fomesafen(1-) + 0
                                  glymidine(1-) + 0
                                  imidazolide 0
                                  rabeprazole(1-) + 0
                                  sulfacetamide(1-) + 0
                                  sulfadiazinate + 0
paths to the root