The structure, properties, distribution in nature, and biological activity of sterol glycosides and acylgylcosides are reviewed.

biological activity, sterol glycoside, acylgylcoside

• Compound ID: 13441
  

  a-D-Glcp-(1-3)-Subst Subst = cholesterol = SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Trivial name: cholesterol 3-O-α-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, steroid glycoside
  
   
  
  Helicobacter felis, Helicobacter muridarum, Helicobacter mustelae, Helicobacter fennelliae
  CSDB ID 64062 (all data & tools)
• Compound ID: 30999
  

  b-D-Glcp-(1-3)-Subst Subst = isofucosterol = SMILES C/C=C(/CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)\C(C)C

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  Structure type: monomer
  Trivial name: isofucosterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Lycopersicon esculentum, Ulva gigantea
  CSDB ID 64056 (all data & tools)
• Compound ID: 17814
  

  b-D-Glcp-(1-3)-Subst Subst = ergosterol = SMILES O{3}[C@@H]4C/C3=C/C=C1\[C@H](CC[C@]2([C@H]1CC[C@@H]2[C@@H](/C=C/[C@H](C)C(C)C)C)C)[C@@]3(C)CC4

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  Structure type: monomer
  C34H56O10
  Trivial name: ergosterol-β-D-glucopyranoside, ergosterol β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, steroid glycoside, sterylglycoside
  Reference(s) to other database(s): GenDB:KT240140
  
   
  
  Hericium erinaceus
  CSDB ID 64057 (all data & tools)
• Compound ID: 13457
  

  b-D-Glcp-(1-3)-Subst Subst = cholesterol = SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Trivial name: cholesterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside
  
   
  
  Candida bogoriensis
  CSDB ID 64061 (all data & tools)
• Compound ID: 30494
  

  b-D-Glcp-(1-6)-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: oligomer
  Trivial name: sterylglycoside SG-I
  Compound class: saponin glycoside
  
   
  
  Musa paradisiaca, Gentiana macrophylla, Vigna angularis
  CSDB ID 64019 (all data & tools)
• Compound ID: 30987
  

  b-D-Glcp-(1-6)-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: oligomer
  Trivial name: α-spinasterol 3-O-gentobioside
  Compound class: saponin glycoside
  
   
  
  
  CSDB ID 64044 (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
  
   
  
  Amarthospermum schomburghinana, Acacia arabica, Gypsophila struthium, Inga edulis var. parviflora, Stellaria dichotoma var. lanceolata, Gynostemma longipes, Prunella vulgaris
  CSDB ID 64041 (all data & tools)
• Compound ID: 30993
  

  b-D-Glcp-(1-3)-Subst Subst = 5,25-stigmastadienol = SMILES C=C(C)[C@@H](CC[C@H](C)C3CCC4C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]34C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Momordica charantia
  CSDB ID 64050 (all data & tools)
• 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
  
   
  
  Prunella vulgaris, Momordica charantia
  CSDB ID 64042 (all data & tools)
• Compound ID: 30995
  

  Pam-(1-6)-b-D-Glcp-(1-3)-Subst Subst = 5,25-stigmastadienol = SMILES C=C(C)[C@@H](CC[C@H](C)C3CCC4C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]34C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Momordica charantia
  CSDB ID 64052 (all data & tools)
• Compound ID: 30996
  

  Ste-(1-6)-b-D-Glcp-(1-3)-Subst Subst = 5,25-stigmastadienol = SMILES C=C(C)[C@@H](CC[C@H](C)C3CCC4C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]34C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Momordica charantia
  CSDB ID 64053 (all data & tools)
• Compound ID: 30962
  

  Pam-(1-6)-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: sitoindoside I
  Compound class: saponin glycoside, glycoside, steroid glycoside
  
   
  
  Musa paradisiaca, Urtica dioica, Vigna angularis, Panax ginseng
  CSDB ID 64015 (all data & tools)
• Compound ID: 30975
  

  Lin-(1-6)-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
  Compound class: saponin glycoside
  
   
  
  Typha latifolia, Panax ginseng
  CSDB ID 64029 (all data & tools)
• Compound ID: 30967
  

  b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-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: oligomer
  Trivial name: β-sitosterol 3-O-gentiotrioside
  Compound class: saponin glycoside
  
   
  
  Vigna angularis
  CSDB ID 64021 (all data & tools)
• Compound ID: 30968
  

  b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-b-D-Glcp-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: oligomer
  Trivial name: stigmasterol 3-O-gentiotrioside
  Compound class: saponin glycoside
  
   
  
  Vigna angularis
  CSDB ID 64022 (all data & tools)
• Compound ID: 30969
  

  b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-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: oligomer
  Trivial name: β-sitosterol 3-O-gentiotrioside
  Compound class: saponin glycoside
  
   
  
  Vigna angularis
  CSDB ID 64023 (all data & tools)
• Compound ID: 30970
  

  b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-b-D-Glcp-(1-6)-b-D-Glcp-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: oligomer
  Trivial name: stigmasterol 3-O-gentiotrioside
  Compound class: saponin glycoside
  
   
  
  Vigna angularis
  CSDB ID 64024 (all data & tools)
• Compound ID: 30998
  

  b-D-Glcp-(1-3)-Subst Subst = stigmasta-7,22,25-trien-3β-ol = SMILES CC[C@@H](C(C)=C)C=C[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
  Compound class: saponin glycoside
  
   
  
  Cucumis sativus
  CSDB ID 64055 (all data & tools)
• Compound ID: 30997
  

  b-D-Galp-(1-3)-Subst Subst = 24β-ethylcholesta-5,22,25-trien-3β-ol = SMILES C[C@H](C=C[C@H](CC)C(C)=C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C{3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Clerodendron inerme
  CSDB ID 64054 (all data & tools)
• Compound ID: 21921
  

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

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  Structure type: monomer
  Trivial name: stigmasterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
  
   
  
  Senecio bonariensis, Prunella vulgaris
  CSDB ID 64012 (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
  
   
  
  Prunella vulgaris
  CSDB ID 64043 (all data & tools)
• Compound ID: 30958
  

  b-D-Xylp-(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: β-sitosterol 3-O-β-D-xylopyranoside
  Compound class: saponin glycoside
  
   
  
  Maytenus senegalensis, Bauhinia candicans
  CSDB ID 64010 (all data & tools)
• Compound ID: 30960
  

  a-D-RibfA-(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: β-sitosterol 3-O-α-D-riburonofuranoside
  Compound class: saponin glycoside
  
   
  
  Bauhinia candicans
  CSDB ID 64013 (all data & tools)
• Compound ID: 30961
  

  a-D-Sugf-(1-3)-Subst Sug = α-D-xylofuranosuronic acid = SMILES O={5}C(O)[C@H]1O{1}[C@H](O){2}[C@H](O){3}[C@H]1O; 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: β-sitosterol 3-O-α-D-xyluronofuranoside
  Compound class: saponin glycoside
  
   
  
  Bauhinia candicans
  CSDB ID 64014 (all data & tools)
• Compound ID: 30959
  

  b-D-GlcpA-(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: β-sitosterol 3-O-β-D-glucuronopyranoside
  Compound class: saponin glycoside
  
   
  
  Senecio bonariensis, Vaccinium scopulorum
  CSDB ID 64011 (all data & tools)
• Compound ID: 30963
  

  Ole-(1-6)-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: sitoindoside II
  Compound class: saponin glycoside
  
   
  
  Musa paradisiaca
  CSDB ID 64016 (all data & tools)
• Compound ID: 30964
  

  Pam-(1-6)-b-D-Glcp-(1-6)-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: oligomer
  Trivial name: sitoindoside III
  Compound class: saponin glycoside
  
   
  
  Musa paradisiaca
  CSDB ID 64017 (all data & tools)
• Compound ID: 30965
  

  Pam-(1-2)-L-myoIno-(1-6)-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: sitoindoside IV
  Compound class: saponin glycoside
  
   
  
  Musa paradisiaca
  CSDB ID 64018 (all data & tools)
• Compound ID: 30966
  

  L-myoIno-(1-6)-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: sterylglycoside SG-II
  Compound class: saponin glycoside
  
   
  
  Musa paradisiaca
  CSDB ID 64020 (all data & tools)
• Compound ID: 30971
  

  Ste-(1-6)-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: β-sitosterol 3-O-6-stearoyl-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Alisma plantago-aquatica, Typha latifolia
  CSDB ID 64025 (all data & tools)
• Compound ID: 30973
  

  aLnn-(1-6)-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
  Compound class: saponin glycoside
  
   
  
  Typha latifolia
  CSDB ID 64027 (all data & tools)
• Compound ID: 30974
  

  gLnn-(1-6)-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
  Compound class: saponin glycoside
  
   
  
  Typha latifolia
  CSDB ID 64028 (all data & tools)
• Compound ID: 30972
  

  Subst-(3-3)-+ | b-D-Fruf-(2-1)-a-D-Glcp 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: oligomer
  Trivial name: β-sitosterol 3-O-β-D-glucopyranosyl-(lα→2)fructofuranoside
  Compound class: saponin glycoside
  
   
  
  Mentha arvensis
  CSDB ID 64026 (all data & tools)
• Compound ID: 30976
  

  b-D-Glcp-(1-4)-a-L-Rhap-(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: oligomer
  Compound class: saponin glycoside
  
   
  
  Gardenia lucida
  CSDB ID 64030 (all data & tools)
• Compound ID: 30977
  

  b-D-Glcp-(1-4)-a-L-Rhap-(1-3)-Subst Subst = campesterol = SMILES O{3}[C@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H]([C@H](C)CC[C@@H](C(C)C)C)CC[C@@]4([H])[C@]3([H])CC=C2C1

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  Structure type: oligomer
  Compound class: saponin glycoside
  
   
  
  Heterophragma quadriloculare
  CSDB ID 64031 (all data & tools)
• Compound ID: 30978
  

  b-D-Glcp-(1-4)-a-L-Rhap-(1-3)-Subst Subst = stigmasta-5,24(28)-diene-3β-ol = SMILES CC(C)/C(CC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C{3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)=C/C

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  Structure type: oligomer
  Compound class: saponin glycoside
  
   
  
  Boswellia serrata
  CSDB ID 64032 (all data & tools)
• Compound ID: 30979
  

  b-D-Galp-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Rhynchosia minima
  CSDB ID 64034 (all data & tools)
• Compound ID: 30980
  

  a-L-Arap-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Walleria yunguensis
  CSDB ID 64035 (all data & tools)
• Compound ID: 30981
  

  Lig-(1-2)-b-D-Xylp-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Asparagus adscendens
  CSDB ID 64036 (all data & tools)
• Compound ID: 30982
  

  b-D-Glcp-(1-2)-a-L-Arap-(1-3)-Subst Subst = stigmasterol = SMILES CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(C)C

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  Structure type: oligomer
  Compound class: saponin glycoside
  
   
  
  Asparagus adscendens
  CSDB ID 64037 (all data & tools)
• Compound ID: 30983
  

  b-D-Glcp-(1-3)-Subst Subst = 24R-ethyl-5α-cholest-7-en-3β-ol = SMILES CC(C)[C@H](CC)CC[C@@H](C)[C@H]1CC[C@@]2([H])C3=CC[C@@]4([H])C{3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Bryonia melanocarpa
  CSDB ID 64038 (all data & tools)
• Compound ID: 30984
  

  b-D-Glcp-(1-3)-Subst Subst = (24E)-stigmasta-7,24(28)-dien-3β-ol = SMILES CC(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)=C/C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Bryonia melanocarpa
  CSDB ID 64039 (all data & tools)
• Compound ID: 30985
  

  b-D-Glcp-(1-3)-Subst Subst = 4α-methyl-24E-stigmasta-7,24(28)-dien-3β-ol = SMILES CC(C)/C(CC[C@@H](C)[C@H]1CC[C@@]2([H])C3=CCC4[C@H](C){3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)=C/C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Bryonia melanocarpa
  CSDB ID 64040 (all data & tools)
• Compound ID: 30991
  

  b-D-Glcp-(1-3)-Subst Subst = stigmast-22-en-3β-ol = SMILES CC[C@@H](C(C)C)C=C[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])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-22-en-3β-ol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Gypsophila struthium
  CSDB ID 64048 (all data & tools)
• Compound ID: 30988
  

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

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  Structure type: monomer
  Trivial name: poriferasterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Sapium insigne, Physarum polycephalum
  CSDB ID 64045 (all data & tools)
• Compound ID: 30989
  

  b-D-Glcp-(1-3)-Subst Subst = (22E,24R)-stigmast-7,22-dien-3α-ol = SMILES CC[C@H](C(C)C)/C=C/[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: (24R)-stigmast-7,22(E)-dien-3α-ol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Mimusops elengi
  CSDB ID 64046 (all data & tools)
• Compound ID: 30990
  

  b-D-Galp-(1-3)-Subst Subst = (22E,24R)-stigmast-7,22-dien-3α-ol = SMILES CC[C@H](C(C)C)/C=C/[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: (24R)-stigmast-7,22(E)-dien-3α-ol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Mimusops elengi
  CSDB ID 64047 (all data & tools)
• Compound ID: 30992
  

  b-D-Glcp-(1-3)-Subst Subst = clerosterol = SMILES CC[C@@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(=C)C

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  Structure type: monomer
  Trivial name: clerosterol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Clerodendrum colebrookianum
  CSDB ID 64049 (all data & tools)
• Compound ID: 30994
  

  b-D-Galp-(1-3)-Subst Subst = clerosterol = SMILES CC[C@@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C)C(=C)C

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  Structure type: monomer
  Trivial name: clerosterol 3-O-β-D-glalactopyranoside
  Compound class: saponin glycoside
  
   
  
  Codium decorticatum
  CSDB ID 64051 (all data & tools)
• Compound ID: 31000
  

  b-D-Glcp-(1-3)-Subst Subst = ergosta-7,22-dien-3β-ol = SMILES C[C@H](C(C)C)C=C[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: ergosta-7,22-dien-3β-ol 3-O-β-D-glucopyranoside
  Compound class: saponin glycoside
  
   
  
  Tylopilus neofelleus
  CSDB ID 64058 (all data & tools)
• Compound ID: 31001
  

  a-L-Fucp-(1-3)-Subst Subst = 24-methylenecholesterol = SMILES CC(C)C(CC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C{3}[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)=C

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  Structure type: monomer
  Trivial name: 24-methylenecholesterol 3-O-α-L-fucopyranoside
  Compound class: saponin glycoside
  
   
  
  Sinularia hirta
  CSDB ID 64059 (all data & tools)
• Compound ID: 31002
  

  b-D-Xylp-(1-3)-Subst Subst = aplysterol = SMILES CC[C@H](C)[C@H](C)CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Trivial name: aplysterol 3-O-β-D-xylopyranoside
  Compound class: saponin glycoside
  
   
  
  Holothuria scabra
  CSDB ID 64060 (all data & tools)
• Compound ID: 13442
  

  Myr-(1-6)-a-D-Glcp-(1-3)-Subst Subst = cholesterol = SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Compound class: glycolipid, saponin glycoside, glycoside
  
   
  
  Helicobacter felis
  CSDB ID 64063 (all data & tools)
• Compound ID: 31003
  

  Lau-(1-6)-a-D-Glcp-(1-3)-Subst Subst = cholesterol = SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Helicobacter muridarum
  CSDB ID 64064 (all data & tools)
• Compound ID: 31004
  

  P-6)-a-D-Glcp-(1-3)-Subst Subst = cholesterol = SMILES C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC{3}[C@@H](C4)O)C)C

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  Structure type: monomer
  Compound class: saponin glycoside
  
   
  
  Helicobacter fennelliae
  CSDB ID 64065 (all data & tools)