- Compound ID: 19262
|
b-D-Glcp-(1-2)-Subst
Subst = magnolol = SMILES C=CCC1=CC={52}C(C(C2={2}C(O)C=CC(CC=C)=C2)=C1)O |
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Structure type: monomer
; 427.18 [M-H]-
C24H22O7
Trivial name: phenolic glycoside
- Compound ID: 19263
|
b-D-Glcp-(1-2)-Subst
Subst = honokiol = SMILES C=CCC1=CC(C2=CC={54}C(C(CC=C)=C2)O)={2}C(O)C=C1 |
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Structure type: monomer
; 473.09 [M+HCOOH-H]-
C30H24O7
Trivial name: phenolic glycoside
- Compound ID: 19264
|
b-D-Glcp-(1-4')-Subst
Subst = honokiol = SMILES C=CCC1=CC(C2=CC={54}C(C(CC=C)=C2)O)={2}C(O)C=C1 |
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Structure type: monomer
; 472.90 [M+HCOOH-H]-
C30H24O7
Trivial name: phenolic glycoside
- Compound ID: 19265
|
b-D-Glcp-(1-3)-Subst
Subst = fisetin = SMILES O=C1{3}C(O)=C(OC2=C1C=C{7}C(O)=C2)C3=CC={54}C({53}C(O)=C3)O |
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Structure type: monomer
; 448.72 [M+H]+
C21H20O11
Trivial name: phenolic glycoside
- Compound ID: 19266
|
b-D-Glcp-(1-8)-Subst
Subst = emodin = SMILES O{1}C(C=C(C=C1C(C2=C3{8}C(O)=C{6}C(O)=C2)=O)C)=C1C3=O |
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Structure type: monomer
; 431.35 [M-H]-
C21H20O10
Trivial name: phenolic glycoside
- Compound ID: 19267
|
b-D-Glcp-(1-3)-Subst
Subst = resveratrol = SMILES O{54}C1=CC=C(/C=C/C2=C{3}C(O)=C{5}C(O)=C2)C=C1 |
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Structure type: monomer
; 390.69 [M+H]+
C22H22O8
Trivial name: phenolic glycoside
- Compound ID: 19268
|
b-D-Glcp-(1-4)-Subst
Subst = 2,4-dihydroxybenzophenone = SMILES O=C(C1={2}C(O)C={4}C(O)C=C1)C2=CC=CC=C2 |
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Structure type: monomer
; 420.65 [M+HCOOH-H]-
C19H20O8
Trivial name: phenolic glycoside
- Compound ID: 19269
|
b-D-Glcp-(1-8)-Subst
Subst = curcumin = SMILES COC1=CC(/C=C/C(CC(/C=C/C2=CC={8}C(C(OC)=C2)O)=O)=O)=CC={58}C1O |
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Structure type: monomer
; 531.02 [M+H]+
C27H30O11
Trivial name: phenolic glycoside
- Compound ID: 19270
|
b-D-Glcp-(1-7)-Subst
Subst = 7-hydroxy-4-methylcoumarin = SMILES Cc1cc(=O)oc2c{7}c(O)ccc12 |
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Structure type: monomer
; 338.93 [M+H]+
C16H18O8
Trivial name: phenolic glycoside