- Compound ID: 19724
|
a-D-Glcp4Me-(1-3)-Subst
Subst = ascosteroside C aglycon = SMILES C=C(CC[C@@H](C)[C@H]1C{15}[C@@H](O)[C@@]2({30}C(=O)O)/C4=C(CC[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(=C)[C@@H]3CC4)C(C)C |
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Structure type: monomer
; 669.3964 [M+Na]+
C37H58O9
Trivial name: ascosteroside A
Compound class: glycoside
- Compound ID: 19725
|
a-D-Glcp4Me-(1-3)-Subst-(30-1)-Me
Subst = ascosteroside C aglycon = SMILES C=C(CC[C@@H](C)[C@H]1C{15}[C@@H](O)[C@@]2({30}C(=O)O)/C4=C(CC[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(=C)[C@@H]3CC4)C(C)C |
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Structure type: monomer
; 683.4113 [M+Na]+
C38H60O9
Compound class: glycoside
- Compound ID: 19726
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Subst1-(7-3)-+
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Subst1-(7-2)-a-D-Glcp4Me-(1-3)-Subst
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Subst1-(7-6)-+
Subst = ascosteroside C aglycon = SMILES C=C(CC[C@@H](C)[C@H]1C{15}[C@@H](O)[C@@]2({30}C(=O)O)/C4=C(CC[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(=C)[C@@H]3CC4)C(C)C;
Subst1 = 4-bromobenzoic acid = SMILES O={7}C(O)c1ccc(Br)cc1 |
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Structure type: monomer
; 1199.2307 [M+Li]+
C58H67O12Br3
Compound class: glycoside
- Compound ID: 19884
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a-D-Glcp4Me-(1-3)-Subst
Subst = ascosteroside C aglycon = SMILES C=C(CC[C@@H](C)[C@H]1C{15}[C@@H](O)[C@@]2({30}C(=O)O)/C4=C(CC[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(=C)[C@@H]3CC4)C(C)C |
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Structure type: monomer
Trivial name: ascosteroside A
Compound class: glycan, glycoside, triterpenoid glycoside
- Compound ID: 20754
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b-D-Glcp4Me-(1-3)-Subst
Subst = ascosteroside C aglycon = SMILES C=C(CC[C@@H](C)[C@H]1C{15}[C@@H](O)[C@@]2({30}C(=O)O)/C4=C(CC[C@]12C)/[C@@]3(C)CC{3}[C@H](O)C(=C)[C@@H]3CC4)C(C)C |
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Structure type: monomer
Trivial name: ascosteroside
Compound class: glycoside