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

ONTOLOGY REPORT - ANNOTATIONS


Term:oseltamivir acid
go back to main search page
Accession:CHEBI:73139 term browser browse the term
Definition:A cyclohexenecarboxylic acid that is cyclohex-1-ene-1-carboxylic acid which is substituted at positions 3, 4, and 5 by pentan-3-yloxy, acetamido, and amino groups, respectively (the 3R,4R,5S enantiomer). An antiviral drug, it is used as the corresponding ethyl ester prodrug, oseltamivir, to slow the spread of influenza.
Synonyms:exact_synonym: (3R,4R,5S)-4-acetamido-5-amino-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylic acid
 related_synonym: Formula=C14H24N2O4;   GS 4071;   InChI=1S/C14H24N2O4/c1-4-10(5-2)20-12-7-9(14(18)19)6-11(15)13(12)16-8(3)17/h7,10-13H,4-6,15H2,1-3H3,(H,16,17)(H,18,19)/t11-,12+,13+/m0/s1;   InChIKey=NENPYTRHICXVCS-YNEHKIRRSA-N;   Ro 64-0802;   SMILES=CCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O;   oseltamivir carboxylate
 xref: CAS:187227-45-8 "ChemIDplus";   PMID:10628898 "Europe PMC";   PMID:21338262 "Europe PMC";   PMID:21495632 "Europe PMC";   PMID:21803598 "Europe PMC";   PMID:22145997 "Europe PMC";   PMID:23000242 "Europe PMC";   PMID:23208436 "Europe PMC";   PMID:23353784 "Europe PMC";   PMID:23362894 "Europe PMC";   PMID:23436258 "Europe PMC";   PMID:23443310 "Europe PMC";   PMID:23459475 "Europe PMC";   PMID:23507284 "Europe PMC";   Reaxys:7714446 "Reaxys"


GViewer not supported for chinchilla.
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
          antiviral agent 0
            antiviral drug 0
              oseltamivir acid 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
                                        monocarboxylic acid 0
                                          acetic acid 0
                                            acetate ester 0
                                              oseltamivir acid 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.