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ONTOLOGY REPORT - ANNOTATIONS


Term:cilostazol
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Accession:CHEBI:31401 term browser browse the term
Definition:A lactam that is 3,4-dihydroquinolin-2(1H)-one in which the hydrogen at position 6 is substiuted by a 4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy group.
Synonyms:exact_synonym: 6-[4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy]-3,4-dihydroquinolin-2(1H)-one
 related_synonym: 6-(4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy)-3,4-dihydro-2(1H)-quinolinone;   6-(4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy)-3,4-dihydrocarbostyril;   6-[4-(1-Cyclohexyl-1H-tetrazol-5-yl)-butoxy]-3,4-dihydro-1H-quinolin-2-one;   Formula=C20H27N5O2;   InChI=1S/C20H27N5O2/c26-20-12-9-15-14-17(10-11-18(15)21-20)27-13-5-4-8-19-22-23-24-25(19)16-6-2-1-3-7-16/h10-11,14,16H,1-9,12-13H2,(H,21,26);   InChIKey=RRGUKTPIGVIEKM-UHFFFAOYSA-N;   SMILES=O=C1CCc2cc(OCCCCc3nnnn3C3CCCCC3)ccc2N1;   cilostazolum
 alt_id: CHEBI:150440
 xref: Beilstein:3632017 "Beilstein";   CAS:73963-72-1 "ChemIDplus";   CAS:73963-72-1 "KEGG DRUG";   DrugBank:DB01166;   Drug_Central:644 "DrugCentral";   KEGG:D01896;   LINCS:LSM-3491
 xref_mesh: MESH:C045645
 xref: PMID:17500510 "ChEMBL";   PMID:9873372 "ChEMBL";   Patent:BE878548;   Patent:US4277479;   VSDB:1939;   Wikipedia:Cilostazol


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  CHEBI ontology 0
    role 0
      application 0
        pharmaceutical 0
          drug 0
            bronchodilator agent 0
              cilostazol 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
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            carbamoyl group 0
                                              carboxamide 0
                                                lactam 0
                                                  cilostazol 0
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