The aerial parts from Blutaparon portulacoides yielded a flavonol whose structure was established as 3,5,3'-trihydroxy-4'-methoxy-6,7-methylenedioxyflavone. In addition, the aerial parts yielded the isoflavone irisone B and the steroids stigmasterol, sitosterol and campesterol. The roots of B. portucaloides furnished sitosteryl, stigmast-7-enyl and spinasteryl β-D-glucopyranosides as well as vanillic acid.

Amaranthaceae, Blutaparon portulacoides, capotiragua, methylenedioxyflavonol

• Compound ID: 20490
  

  b-D-Glcp-(1-3)-Subst Subst = β-sitosterol = SMILES O{3}[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@@]2([H])CC[C@@]4(C)[C@]3([H])CC[C@]4([C@@H](C)CC[C@@H](CC)C(C)C)[H]

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  Structure type: monomer
  Trivial name: daucosterol, β-daucosterol, β-sitosterol, β-sitosterol-β-D-glucoside, androsine, saxifragifolin B, β-sitosterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
  Reference(s) to other database(s): GenDB:MK026953.1
  
   
  
  Blutaparon portulacoides
  CSDB ID 65452 (all data & tools)
• Compound ID: 30057
  

  b-D-Glcp-(1-3)-Subst Subst = α-spinasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: monomer
  Trivial name: α-spinasterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, triterpenoid glycoside
  
   
  
  Blutaparon portulacoides
  CSDB ID 65454 (all data & tools)
• Compound ID: 30986
  

  b-D-Glcp-(1-3)-Subst Subst = stigmast-7-en-3β-ol = SMILES CC[C@@H](C(C)C)CC[C@@H](C)[C@H]1CC[C@@]2([H])C3=CCC4C{3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C

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  Structure type: monomer
  Trivial name: stigmast-7-en-3β-ol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, triterpenoid glycoside
  
   
  
  Blutaparon portulacoides
  CSDB ID 65453 (all data & tools)