Found 11 structures.
Displayed structures from 1 to 11
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1. Compound ID: 33546
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b-D-Glcp-(1-1)-+
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Subst-(9-3)-a-L-Rhap-(1-6)-Catalpol
Subst = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: oligomer
Compound class: glycoside, iridoid glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12920
de Sandos J, Fernandez L, Díaz AM, Rubio B, Olivier E, Fauer R, Balansard G "Catalpol glycosides from Scrophularia scorodonia" -
Die Pharmazie 53(6) (1998) 427-428
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Laboratory of Pharmacognosy, Faculty of Pharmacy, University of Alcalá de Henares Madrid, Spain, Laboratory of Pharmacognosy, Faculty of Pharmacy, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France, URA 14111, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France
Methods: extraction, CC, MPLC
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2. Compound ID: 33547
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b-D-Glcp-(1-1)-+
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pCoum-(9-4)-+ |
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pCoum-(9-3)-a-L-Rhap2Ac-(1-6)-Catalpol |
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Structure type: oligomer
Trivial name: scropolioside
Compound class: glycoside, iridoid glycoside
Contained glycoepitopes: IEDB_116879,IEDB_130422,IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12920
de Sandos J, Fernandez L, Díaz AM, Rubio B, Olivier E, Fauer R, Balansard G "Catalpol glycosides from Scrophularia scorodonia" -
Die Pharmazie 53(6) (1998) 427-428
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Laboratory of Pharmacognosy, Faculty of Pharmacy, University of Alcalá de Henares Madrid, Spain, Laboratory of Pharmacognosy, Faculty of Pharmacy, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France, URA 14111, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France
Methods: extraction, CC, MPLC
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3. Compound ID: 33548
Structure type: monomer
Trivial name: 6-methoxycatalpol
Compound class: glycoside, iridoid glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12920
de Sandos J, Fernandez L, Díaz AM, Rubio B, Olivier E, Fauer R, Balansard G "Catalpol glycosides from Scrophularia scorodonia" -
Die Pharmazie 53(6) (1998) 427-428
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Laboratory of Pharmacognosy, Faculty of Pharmacy, University of Alcalá de Henares Madrid, Spain, Laboratory of Pharmacognosy, Faculty of Pharmacy, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France, URA 14111, University Aix-Marseille III Avenue Escadrille Normandie Niemen, Marseille, France
Methods: extraction, CC, MPLC
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4. Compound ID: 33549
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b-D-Glcp-(1-28)-Subst
Subst = 2α,3β,19α-trihydroxyolean-12-ene-24,28-dioic acid |
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Structure type: monomer
Compound class: glycoside, triterpenoid glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12922
Fontana N, Bisio A, Romussi G "Triterpene saponins and flavonoids from Quercus glauca Thun. Part 233: Constituents of fagaceae (Cupuliferae)" -
Die Pharmazie 53(9) (1998) 653-654
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Genoa University, Italy, Istituto Botanico Hanbury, Genoa University, Italy
Methods: TLC, extraction, CC, evaporation, DCCC
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5. Compound ID: 33550
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b-D-Glcp-(1-28)-Subst
Subst = 2α,3β,19α-trihydroxyurs-12-ene-24,28-dioic acid |
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Structure type: monomer
Trivial name: trachelosperoside A-1
Compound class: glycoside, triterpenoid glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12922
Fontana N, Bisio A, Romussi G "Triterpene saponins and flavonoids from Quercus glauca Thun. Part 233: Constituents of fagaceae (Cupuliferae)" -
Die Pharmazie 53(9) (1998) 653-654
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Genoa University, Italy, Istituto Botanico Hanbury, Genoa University, Italy
Methods: TLC, extraction, CC, evaporation, DCCC
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6. Compound ID: 33551
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
Contained glycoepitopes: IEDB_116879,IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12922
Fontana N, Bisio A, Romussi G "Triterpene saponins and flavonoids from Quercus glauca Thun. Part 233: Constituents of fagaceae (Cupuliferae)" -
Die Pharmazie 53(9) (1998) 653-654
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Genoa University, Italy, Istituto Botanico Hanbury, Genoa University, Italy
Methods: TLC, extraction, CC, evaporation, DCCC
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7. Compound ID: 33552
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pCoum-(9-6)-+
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Subst-(9-4)-b-D-Glcp2Ac3Ac-(1-3)-Kaempferol
Subst = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
Contained glycoepitopes: IEDB_116879,IEDB_142488,IEDB_146664,IEDB_983931,SB_192,SB_61
The structure is contained in the following publication(s):
- Article ID: 12922
Fontana N, Bisio A, Romussi G "Triterpene saponins and flavonoids from Quercus glauca Thun. Part 233: Constituents of fagaceae (Cupuliferae)" -
Die Pharmazie 53(9) (1998) 653-654
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Genoa University, Italy, Istituto Botanico Hanbury, Genoa University, Italy
Methods: TLC, extraction, CC, evaporation, DCCC
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8. Compound ID: 33553
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
Contained glycoepitopes: IEDB_116879,IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12922
Fontana N, Bisio A, Romussi G "Triterpene saponins and flavonoids from Quercus glauca Thun. Part 233: Constituents of fagaceae (Cupuliferae)" -
Die Pharmazie 53(9) (1998) 653-654
Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Genoa University, Italy, Istituto Botanico Hanbury, Genoa University, Italy
Methods: TLC, extraction, CC, evaporation, DCCC
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9. Compound ID: 33554
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b-D-Glcp-(1-4)-b-D-Xylp-(1-3)-Subst14Me
Subst = hyrcanoside aglycon = SMILES C[C@]12CC[C@H]3[C@@H](CCC4=C{3}[C@@H](O)CC[C@]34C=O){14}[C@@]1(O)CCC2C5=CC(OC5)=O |
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Structure type: oligomer
Trivial name: 14-methoxyhyrcanoside
Compound class: glycoside
Contained glycoepitopes: IEDB_114701,IEDB_142488,IEDB_146664,IEDB_167188,IEDB_174332,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12923
Ali AA, Mohamed MH, Kamel MS, Fouad MA, Spring O "Studies on Securigera securidacea (L.) Deg. et Dorfl. (Fabaceae) seeds, an antidiabetic Egyptian folk medicine" -
Die Pharmazie 53(10) (1998) 710-715
A new cardenolide(-)-14-methoxyhyrcanoside (1) was isolated from the aqueous extract of the seeds of Securigera securidacea (L.) Deg. et Dörfl. (Fabaceae) together with five new dihydrobenzofuran derivatives named securigran I-V (2-6). Kaempferol and astragalin were also isolated from the aqueous extract of the flowers. (-)-14-Methoxyhyrcanoside and the total aqueous extract of the seeds showed marked chronotropic activity. The total aqueous extract also showed a marked diuretic and severe hypokalemic effects on the K(+)-level in serum. The hypoglycemic effect of the seeds was also confirmed.
NCBI PubMed ID: 9812339Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Pharmacognosy Department, Faculty of Pharmacy, Assiut University, Assiut, Egypt
Methods: 13C NMR, 1H NMR, TLC, ESI-MS, HPLC, extraction
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10. Compound ID: 33555
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b-D-Glcp-(1-4)-b-D-Xylp-(1-3)-Subst
Subst = hyrcanoside aglycon = SMILES C[C@]12CC[C@H]3[C@@H](CCC4=C{3}[C@@H](O)CC[C@]34C=O){14}[C@@]1(O)CCC2C5=CC(OC5)=O |
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Structure type: oligomer
Trivial name: hyrcanoside
Compound class: glycoside
Contained glycoepitopes: IEDB_114701,IEDB_142488,IEDB_146664,IEDB_167188,IEDB_174332,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12923
Ali AA, Mohamed MH, Kamel MS, Fouad MA, Spring O "Studies on Securigera securidacea (L.) Deg. et Dorfl. (Fabaceae) seeds, an antidiabetic Egyptian folk medicine" -
Die Pharmazie 53(10) (1998) 710-715
A new cardenolide(-)-14-methoxyhyrcanoside (1) was isolated from the aqueous extract of the seeds of Securigera securidacea (L.) Deg. et Dörfl. (Fabaceae) together with five new dihydrobenzofuran derivatives named securigran I-V (2-6). Kaempferol and astragalin were also isolated from the aqueous extract of the flowers. (-)-14-Methoxyhyrcanoside and the total aqueous extract of the seeds showed marked chronotropic activity. The total aqueous extract also showed a marked diuretic and severe hypokalemic effects on the K(+)-level in serum. The hypoglycemic effect of the seeds was also confirmed.
NCBI PubMed ID: 9812339Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Pharmacognosy Department, Faculty of Pharmacy, Assiut University, Assiut, Egypt
Methods: 13C NMR, 1H NMR, TLC, ESI-MS, HPLC, extraction
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11. Compound ID: 33556
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b-D-Glcp-(1-2)-+
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b-D-Glcp-(1-3)-Subst2Me-(7-7)-Subst1
Subst = 2,3,6-trihydroxybenzoic acid = SMILES O={7}C(O)C1={6}C(O)C=C{3}C(O)={2}C1O;
Subst1 = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: oligomer
Trivial name: leiocarposide
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 12924
Bader G, Lück L, Schenk R, Hirschelmann R, Hiller K "Leiocarposide - Lead structure for the quality assurance of solidaginis virgaureae herba" -
Die Pharmazie 53(11) (1998) 805-806
NCBI PubMed ID: 9853363Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Institutions: Institut für Pharmazie, Mathematisch-Naturwissenschafliche Fakultät I, Humboldt-Universität zu Berlin, Berlin, Germany, Institut für Pflanzenbauwissenschaften, Landwirtschaftlich-Gärtnerische Fakultät, Humboldt-Universität zu Berlin, Berlin, Germany, Fachbereich Pharmazie, Martin-Luther Universität Halle-Wittenberg, Halle, Germany
Methods: HPLC, extraction
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Total list of structure IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
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