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1. (Article ID: 11504)
Yamamoto H, Yoshida K, Kondo Y, Inoue K
Production of cornoside in Abeliophyllum distichum cell suspension cultures
Phytochemistry 48(2) (1998)
273-277
The production of phenylethanoid derivatives in callus and cell suspension cultures of four oleaceous plants, Abeliophyllum distichum, Forsythia suspensa, F. viridissima, and F. koreana was investigated. Of two types of A. distichum cultured cells, the friable fine cells produced only the 4-hydroxyphenylethanoid-type glucoside, cornoside, whereas the small cell aggregates produced the 3,4-dihydroxyphenylethanoid-type glycosides (i.e. verbascoside) predominantly. In the cultured cells of F. suspensa and F. viridissima, the latter-type glycosides were produced predominantly and from those of F. koreana, lignan glucosides with 3,4-dioxygenated phenyl groups were isolated.
production, Forsythia suspensa, Oleaceae, cornoside, Abeliophyllum distichum, benzoquinolethanoid glucoside, cell suspension cultures, F. koreana, F. viridissima, phenylethanoid glycosides
Publication DOI: 10.1016/S0031-9422(97)01134-5Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Department of Pharmacognosy, Gifu Pharmaceutical University, Gifu, Japan
Methods: extraction, CC, RP-HPLC
The publication contains the following compound(s):
- Compound ID: 22429
Structure type: oligomer
Trivial name: acteoside, verbascoside, acteoside, verbascoside, trans-verbascoside, verbascoside, acteoside
Compound class: saponin glycoside, glycoside, phenolic glycoside, phenylethanoid glycoside, phenylpropanoid glycoside, iridoid glycoside, lignan glycoside
- Compound ID: 29460
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b-D-Xylp-(1-6)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet
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Caf-(9-4)-+ |
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Structure type: oligomer
Trivial name: arenarioside
Compound class: glycoside, phenolic glycoside, phenylethanoid glycoside, phenylpropanoid glycoside
- Compound ID: 29461
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b-D-Glcp-(1-8)-Subst
Subst = cornoside aglycone = SMILES O=C/1/C=C\{4}C(O)(C{8}CO)\C=C1 |
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Structure type: monomer
Trivial name: cornoside
Compound class: glycoside
- Compound ID: 29462
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b-D-Glcp-(1-4')-Subst4Me
Subst = matairesinol = SMILES COC1={4}C(O)C=CC(C[C@H]2COC([C@@H]2CC3=CC(OC)={54}C(O)C=C3)=O)=C1 |
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Structure type: oligomer
Trivial name: arctiin
Compound class: glycoside
- Compound ID: 29463
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b-D-Glcp-(1-4')-Subst
Subst = matairesinol = SMILES COC1={4}C(O)C=CC(C[C@H]2COC([C@@H]2CC3=CC(OC)={54}C(O)C=C3)=O)=C1 |
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Structure type: oligomer
Trivial name: matairesinol 4'-O-glucoside
Compound class: glycoside
- Compound ID: 29464
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b-D-Glcp-(1-4')-Subst
Subst = epipinoresinol = SMILES COc4ccc(C1OCC2C1COC2c3cc{54}c(O)c(OC)c3)c{103}c4O |
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Structure type: oligomer
Trivial name: epipinoresinol 4'-o-glucoside
Compound class: glycoside
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2. (Article ID: 11834)
Seigler DS, Spencer KC, Statler WS, Conn EE, Dunn JE
Tetraphyllin B and epitetraphyillin B sulphates: novel cyanogenic glucosides from Passiflora caerulea and P. alato-caerulea
Phytochemistry 21(9) (1982)
2277-2285
An epimeric mixture of tetraphyllin B-4-sulphate and epitetraphyllin B-4-sulphate was isolated from Passiflora caerulea and P. alato-caerulea.
NMR, Passifloraceae, cyanogenic glycoside, Passiflora caerulea, P. alato-caerulea, cyanogenic glycoside sulphate, tetraphyllin B, tetraphyllin B sulfate
Publication DOI: 10.1016/0031-9422(82)85191-1Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Department of Botany, University of Illinois, Urbana, Illinois, USA, Department of Biochemistry and Biophysics, University of California, Davis, California, USA
Methods: 13C NMR, 1H NMR, TLC, enzymatic hydrolysis, GLC, electrophoresis, acetylation, dialysis, FD-MS, trimethylsilylation
The publication contains the following compound(s):
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