Found 2 publications.
Displayed publications from 1 to 2
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 12078)
Chiba M, Hisada S, Nishibe S, Thieme H
13C NMR analysis of symplocosin and (+)-epipinoresinol glucoside
Phytochemistry 19 (1980)
335-336
The structures are described of (-)-epipinoresinol-β-D-glucoside (symplocosin) from Symplocos lucida and (+)-epipinoresinol-β-D-glucoside from Forsythia sp.
13C NMR, Oleaceae, lignans, Symplocos lucida, Symplocaceae, Forsythia species, epipinoresinol-β-D-glucoside
Publication DOI: 10.1016/S0031-9422(00)81990-1Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Faculty of Pharmaceutical Sciences, Higashi Nippon Gakuen University, Ishikari-Tobetsu, Japan, Sektion Biowissenschaften der Karl-Marx-Universität, Leipzig, Germany
Methods: 13C NMR
The publication contains the following compound(s):
- Compound ID: 22478
|
b-D-Glcp-(1-4')-Subst
Subst = (+)-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2[C@@]3([H])CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
C26H32O11
Compound class: glycoside, lignan, lignan glycoside
- Compound ID: 30520
|
b-D-Glcp-(1-4)-Subst4'Me
Subst = (+)-epipinoresinol = SMILES COc1cc([C@H]2OC[C@@H]3[C@H](c4cc{4}c(O)c(OC)c4)OC[C@H]23)cc{54}c1O |
Show graphically |
Structure type: monomer
C27H34O11
Trivial name: phillyrin
Compound class: glycoside, lignan, lignan glycoside, lignan glucoside
- Compound ID: 31440
|
b-D-Glcp-(1-4')-Subst
Subst = (-)-epipinoresinol = SMILES COC1={54}C(C=CC([C@H]2[C@@H]3CO[C@@H]([C@@H]3CO2)C4=CC(OC)={4}C(C=C4)O)=C1)O |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan
- Compound ID: 31441
|
b-D-Glcp-(1-4')-Subst
Subst = (+)-epipinoresinol = SMILES COc1cc([C@H]2OC[C@@H]3[C@H](c4cc{4}c(O)c(OC)c4)OC[C@H]23)cc{54}c1O |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan
- Compound ID: 31442
|
b-D-Glcp-(1-4')-Subst4"Me
Subst = (+)-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2[C@@]3([H])CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan, lignan glycoside
Expand this publication
Collapse this publication
2. (Article ID: 12525)
Nikaido T, Ohmoto T, Kinoshita T, Sankawa U, Nishibe S, Hisada S
Inhibition of cyclic AMP phosphodiesterase by lignans
Chemical and Pharmaceutical Bulletin 29(12) (1981)
3586-3592
Cyclic adenosine monophosphate (AMP) phosphodiesterase inhibitors contained in Forsythia suspensa were identified as lignans, (+)-pinoresinol (Ia) and (+)-pinoresinol-β-D-glucoside (Id), and their structure-activity relationship was investigated. In pinoresinol congeners, the configuration of the two phenyl rings is very important in relation to the activity. When both of the p-hydroxyl groups in matairesinol congeners are substituted by methyl or glucose, the activities are decreased as compared with those of the unsubstituted compounds.
inhibitors, Forsythia suspensa, lignans, cAMP phosphodiesterase, (+)-pinoresinol, (+)-pinoresinol-β-D-glucoside, (-)-matairesinol
NCBI PubMed ID: 6280885Publication DOI: 10.1248/cpb.29.3586Journal NLM ID: 0377775Publisher: Pharmaceutical Society Of Japan
Institutions: Faculty of Pharmaceutical Sciences, University of Tokyo, Tokyo, Japan, Faculty of Pharmaceutical Sciences, Higashi Nippon Gakuen University, Ishikari-Tobetsu, Japan, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan
Methods: inhibition studies, biological assays
The publication contains the following compound(s):
- Compound ID: 26810
|
b-D-Glcp-(1-4")-Subst
Subst = (+)-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2[C@@]3([H])CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan glycoside
Reference(s) to other database(s): CCSD:
42554, CBank-STR:1012
- Compound ID: 30520
|
b-D-Glcp-(1-4)-Subst4'Me
Subst = (+)-epipinoresinol = SMILES COc1cc([C@H]2OC[C@@H]3[C@H](c4cc{4}c(O)c(OC)c4)OC[C@H]23)cc{54}c1O |
Show graphically |
Structure type: monomer
C27H34O11
Trivial name: phillyrin
Compound class: glycoside, lignan, lignan glycoside, lignan glucoside
- Compound ID: 27136
|
b-D-Glcp-(1-4')-+
|
b-D-Glcp-(1-4")-Subst
Subst = (+)-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2[C@@]3([H])CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: oligomer
Compound class: saponin glycoside, glycoside, lignan glycoside
- Compound ID: 31439
|
b-D-Glcp-(1-4')-Subst1Ac
Subst = (+)-1-hydroxy-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2{1}[C@@]3(O)CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
C28H34O13
Compound class: glycoside, lignan, lignan glycoside
- Compound ID: 31546
|
b-D-Glcp-(1-4')-Subst
Subst = (+)-1-hydroxy-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2{1}[C@@]3(O)CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan, lignan glycoside
- Compound ID: 32493
|
b-D-Glcp-(1-4')-Subst1Ac4"Me
Subst = (+)-1-hydroxy-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2{1}[C@@]3(O)CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 32494
|
b-D-Glcp-(1-4')-Subst4"Me
Subst = (+)-1-hydroxy-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2{1}[C@@]3(O)CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 32495
|
b-D-Glcp-(1-1)-Subst
Subst = (+)-1-hydroxy-pinoresinol = SMILES O{54}C1=C(OC)C=C([C@@H]2{1}[C@@]3(O)CO[C@H](C4=CC(OC)={104}C(O)C=C4)[C@@]3([H])CO2)C=C1 |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 21918
|
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 |
Show graphically |
Structure type: monomer
C27H34O11
Trivial name: arctiin
Compound class: glycoside, lignan glycoside
- Compound ID: 32091
|
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 |
Show graphically |
Structure type: monomer
C26H32O11
Trivial name: matairesinoside
Compound class: glycoside, lignan glycoside
- Compound ID: 32496
|
b-D-Glcp-(1-4')-Subst
Subst = (-)-pinoresinol = SMILES COc1cc(cc{104}c1O)[C@H]2[C@@H]3CO[C@H]([C@@H]3CO2)c4cc{54}c(c(c4)OC)O |
Show graphically |
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 30519
|
b-D-Glcp-(1-4)-Subst
Subst = (+)-epipinoresinol = SMILES COc1cc([C@H]2OC[C@@H]3[C@H](c4cc{4}c(O)c(OC)c4)OC[C@H]23)cc{54}c1O |
Show graphically |
Structure type: monomer
Trivial name: simplocosin
Compound class: glycoside, lignan glycoside, lignan glucoside
- Compound ID: 32497
|
b-D-Glcp-(1-4)-+
|
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 |
Show graphically |
Structure type: oligomer
C32H42O16
Compound class: glycoside, lignan glycoside
- Compound ID: 32498
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 32499
Structure type: monomer
Compound class: glycoside, lignan glycoside
- Compound ID: 32500
|
b-D-Glcp-(1-4)-+
|
b-D-Glcp-(1-4')-Subst
Subst = 1-hydroxymatairesinol |
Show graphically |
Structure type: oligomer
Compound class: glycoside, lignan glycoside
- Compound ID: 22479
|
b-D-Glcp-(1-4')-+
|
b-D-Glcp-(1-4")-Subst
Subst = (+)-syringaresinol = SMILES COC1=CC([C@@H]2[C@@]3([H])CO[C@H](C4=CC(OC)={104}C(O)C(OC)=C4)[C@@]3([H])CO2)=CC(OC)={54}C1O |
Show graphically |
Structure type: oligomer
Trivial name: liriodendrin
Compound class: glycoside, lignan glycoside
Reference(s) to other database(s): CCSD:
46086, CBank-STR:2954
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec