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: 10741)
Fauvel MT, Bousquet-Melou A, Moulis C, Gleye J, Jensen SR
Iridoid glucosides from Avicennia germinans
Phytochemistry 38 (1995)
893-894
A new iridoid glucoside, namely 2′-caffeoyl mussaenosidic acid has been isolated from leaves of Avicennia germinans along with the known compounds 2′-cinnamoyl mussaenosidic acid and verbascoside. The structure of the new compound was established by spectroscopic methods.
iridoid glucosides, Avicennia germinans, Avicenniaceae/Verbenaceae, 2′-cinnamoyl mussaenosidic acid, 2′-caffeoyl mussaenosidic acid, verbascoside
Publication DOI: 10.1016/0031-9422(94)00750-NJournal NLM ID: 0151434Publisher: Elsevier
Institutions: Institut de la Carte Internationale de la Végétation, Toulouse, France, EA820 “Substances naturelles à visée antiparasitaire” Faculté des Sciences Pharmaceutiques 35 chemin des Maraîchers, Toulouse, France, Department of Organic Chemistry, Technical University of Denmark, Lyngby, Denmark
Methods: 13C NMR, 1H NMR, IR, FAB-MS, CC
The publication contains the following compound(s):
- Compound ID: 25863
|
Caf-(9-4)-+
|
a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet
Caf = caffeic acid;
3,4,8HOPhet = phenylethane-3,4,8-triol |
Show graphically |
Structure type: oligomer
Trivial name: acteoside verbascoside, acteoside, verbascoside
Compound class: saponin glycoside, glycoside, phenolic glycoside, flavonol glycoside, phenylethanoid glycoside
Reference(s) to other database(s): CCSD:
50837, CBank-STR:5112
- Compound ID: 26744
|
Cin-(9-2)-b-D-Glcp-(1-1)-Subst
Subst = mussaenosidic acid aglycon = SMILES C{10}[C@]1(O)CC[C@H]2[C@@H]1{1}[C@H](O)OC=C2{11}C(O)=O;
Cin = cinnamic acid |
Show graphically |
Structure type: monomer
; 539 [M+Na]+
Compound class: glycoside
Reference(s) to other database(s): CCSD:
41309, CBank-STR:2329
- Compound ID: 26745
|
Caf-(9-2)-b-D-Glcp-(1-1)-Subst
Subst = mussaenosidic acid aglycon = SMILES C{10}[C@]1(O)CC[C@H]2[C@@H]1{1}[C@H](O)OC=C2{11}C(O)=O;
Caf = caffeic acid |
Show graphically |
Structure type: monomer
; 556 [M+NH4]+
Compound class: glycoside
Reference(s) to other database(s): CCSD:
41310, CBank-STR:2321
Expand this publication
Collapse this publication
2. (Article ID: 11682)
Fauvel MT, Bon M, Crasnier F, Moulis C, Fouraste I
Megastigmane and iridoid glucosides from Avicennia germinans: two isomeric forms of an iridoid
Natural Product Letters 14(2) (1999)
99-106
The iridoid 2′-coumaroyl mussaenosidic acid, isolated from Avicennia germinans (Avicenniaceae), was analysed by NMR and molecular modeling: two isomeric forms were confirmed. In addition, the known compound 1 (6S, 9R) roseoside was isolated for the first time from this species of Avicennia.
NMR, molecular modeling, iridoid, Avicennia germinans, Avicenniaceae, megastigmane glucoside vomifoliol 9-O-β-D-Glucopyranoside (roseoside), 2′-coumaroyl mussaenosidic acid
Publication DOI: 10.1080/10575639908041216Journal NLM ID: 9315615Publisher: Taylor & Francis Health Sciences
Institutions: Laboratoire d'Ecologic Terrestre CNRS/UPS, 13 avenue du Colonel Roche F-31405, Toulouse, France, Institut de Chimie Moleculaire (FU14) Université Paul Sabatier, 118 route de Narbonne F-31062, Toulouse, France, UPRES EA 820 ''Substances Naturelles à Visée Antiparasitaire'' Faculté des Sciences Pharmaceutiques, 35 Chemin des Maraichers F-31062, Toulouse, France
Methods: 13C NMR, 1H NMR, TLC, molecular modeling, CID-MS, molecular mechanics, HMBC, HMQC, COSY
The publication contains the following compound(s):
- Compound ID: 30061
|
b-D-Glcp-(1-9)-Subst
Subst = blumenol C = SMILES O=C1CC(C)([C@H](C(C)=C1)CC{9}[C@@H](C)O)C |
Show graphically |
Structure type: monomer
; 387 [M+H]+
Trivial name: roseoside
Compound class: iridoid glycoside
- Compound ID: 30062
|
pCoum-(9-2)-b-D-Glcp-(1-1)-Subst
Subst = mussaenosidic acid aglycon = SMILES C{10}[C@]1(O)CC[C@H]2[C@@H]1{1}[C@H](O)OC=C2{11}C(O)=O |
Show graphically |
Structure type: monomer
Compound class: iridoid glycoside
- Compound ID: 30063
|
Subst1-(9-2)-b-D-Glcp-(1-1)-Subst2
Subst1 = cis-cinnamic acid = SMILES O={9}C(O)/C=C\C1=CC=CC=C1;
Subst2 = mussaenosidic acid aglycon = SMILES C{10}[C@]1(O)CC[C@H]2[C@@H]1{1}[C@H](O)OC=C2{11}C(O)=O |
Show graphically |
Structure type: monomer
Compound class: iridoid glycoside
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