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Term:anagalligenin A
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Accession:CHEBI:71347 term browser browse the term
Definition:A hexacyclic triterpenoid that is an oleanane substituted by an epoxy group between positions 13 and 28 and by hydroxy groups at positions 3, 16, 22 and 28 respectively (the 3beta,16alpha,22alpha stereoisomer). It is isolated from the whole plant of Anagallis arvensis.
Synonyms:exact_synonym: (3beta,16alpha,22alpha)-13,28-epoxyoleanane-3,16,22,28-tetrol
 related_synonym: Formula=C30H50O5;   InChI=1S/C30H50O5/c1-24(2)14-19-29-13-9-18-26(5)11-10-20(31)25(3,4)17(26)8-12-27(18,6)28(29,7)16-22(33)30(19,21(32)15-24)23(34)35-29/h17-23,31-34H,8-16H2,1-7H3/t17-,18+,19-,20-,21-,22+,23+,26-,27+,28-,29-,30-/m0/s1;   InChIKey=HUTBSECGWQRLCI-OWYJUUJQSA-N;   SMILES=[H][C@]1(O)CC[C@@]2(C)[C@@]([H])(CC[C@]3(C)[C@]2([H])CC[C@]24O[C@@H](O)[C@@]5([C@@H](O)CC(C)(C)C[C@@]25[H])[C@H](O)C[C@@]34C)C1(C)C
 xref: PMID:16595968 "Europe PMC"

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  CHEBI ontology 23805
    role 23692
      biological role 23655
        biochemical role 23000
          metabolite 22895
            anagalligenin A 0
              capilliposide B 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 23805
    subatomic particle 23756
      composite particle 23756
        hadron 23756
          baryon 23756
            nucleon 23756
              atomic nucleus 23756
                atom 23756
                  main group element atom 23575
                    main group molecular entity 23575
                      s-block molecular entity 22754
                        hydrogen molecular entity 22551
                          hydrides 20649
                            organic hydride 19727
                              organic fundamental parent 19727
                                hydrocarbon 19029
                                  terpene 9717
                                    triterpene 659
                                      triterpenoid 654
                                        hexacyclic triterpenoid 112
                                          anagalligenin A 0
                                            capilliposide B 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.