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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:sangivamycin
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Accession:CHEBI:85997 term browser browse the term
Definition:A nucleoside analogue that is adenosine in which the nitrogen at position 7 is replaced by a carbamoyl-substituted carbon. It is a potent inhibitor of protein kinase C.
Synonyms:exact_synonym: 4-amino-7-beta-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxamide
 related_synonym: 7-Deaza-7-carbamoyladenosine;   7-Deazaadenosine-7-carboxamide;   Formula=C12H15N5O5;   InChI=1S/C12H15N5O5/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16)/t5-,7-,8-,12-/m1/s1;   InChIKey=OBZJZDHRXBKKTJ-JTFADIMSSA-N;   SMILES=NC(=O)c1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2ncnc(N)c12
 xref: Beilstein:626355;   CAS:18417-89-5;   PMID:26024233;   PMID:3338987;   Reaxys:626355


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  CHEBI ontology 0
    role 0
      biological role 0
        pharmacological role 0
          analgesic 0
            adenosine 0
              sangivamycin 0
Path 2
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  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
                            heteroorganic entity 0
                              organochalcogen compound 0
                                organooxygen compound 0
                                  carbohydrates and carbohydrate derivatives 0
                                    carbohydrate 0
                                      carbohydrate derivative 0
                                        glycosyl compound 0
                                          N-glycosyl compound 0
                                            nucleoside 0
                                              ribonucleoside 0
                                                purine ribonucleoside 0
                                                  purines D-ribonucleoside 0
                                                    adenosine 0
                                                      sangivamycin 0
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