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1. (Article ID: 11801)
Cuendet M, Potterat O, Hostettmann K
Iridoid glucosides, phenylpropanoid derivatives and flavonoids from Bartsia alpina
Pharmaceutical Biology 37(4) (1999)
318-320
Three iridoid glucosides, two phenylpropanoid derivatives and one flavonoid have been isolated from the methanolic whole plant extract of Bartsia alpina L. (Scrophulariaceae). Their structures were established by spectrometric (UV, D/CI and FAB mass spectrometry, 1H and 13C NMR) and chemical methods. Some of these compounds have radical scavenging activity against DPPH or antioxidant activity against beta-carotene on TLC bioassay.
flavonoid, Antioxidant activity, radical scavenging activity, Scrophulariaceae, Iridoids, phenylpropanoid derivatives, Bartsia alpina
Publication DOI: 10.1076/phbi.37.4.318.5808Journal NLM ID: 9812552Publisher: Lisse, the Netherlands: Swets & Zeitlinger
Correspondence: Hostettmann K
ipp.unil.ch>
Institutions: Institut de Pharmacognosie et Phytochimie, Université de Lausanne, BEP, CH-1015 Lausanne, Switzerland
Methods: 13C NMR, 1H NMR, TLC, UV, antioxidant activities, MPLC, HPLC-UV
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: 23824
Structure type: oligomer
Trivial name: glucoluteolin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
27029, CBank-STR:939
- Compound ID: 27208
|
b-D-Glcp-(1-1)-Subst11Me
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 |
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Structure type: monomer
Trivial name: mussaenoside, penstemide
Compound class: glycoside, iridoid glycoside
Reference(s) to other database(s): CCSD:
49802, CBank-STR:1149
- Compound ID: 27302
|
b-D-Glcp-(1-1)-Subst
Subst = aucubin aglycon = SMILES O{10}CC1=C{6}[C@@H](O)[C@H]2[C@@H]1{1}[C@H](O)OC=C2 |
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Structure type: monomer
Trivial name: aucubin
Compound class: glycoside, iridoid glycoside
Reference(s) to other database(s): CCSD:
50098, CBank-STR:1313, PubChem:91458
- Compound ID: 29555
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a-L-Rhap-(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: poliumoside
Compound class: glycoside, phenylpropanoid glycoside
- Compound ID: 30495
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b-D-Glcp-(1-1)-Subst10Bz
Subst = aucubin aglycon = SMILES O{10}CC1=C{6}[C@@H](O)[C@H]2[C@@H]1{1}[C@H](O)OC=C2 |
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Structure type: monomer
Trivial name: melampyroside, 10-benzoylaucubin, melampyroside, 10-benzoylaucubin
Compound class: glycoside, iridoid glycoside
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