Acteoside (verbascoside) was isolated as an analgesic principle from Cedron (leaves and stem of Lippia triphylla (L'HER) O. KUNTZE; Verbenaceae), a Peruvian medicinal plant, by activity-guided separation. The compound exhibited analgesia on acetic acid-induced writhing and on tail pressure pain in mice by the oral administration of 300 mg/kg and 100 mg/kg, respectively. Acteoside also caused weak sedation by its effect on the prolongation of pentobarbital-induced anesthesia and on the depression of locomotion enhanced by methamphetamine. An intravenous injection of acteoside reduced the effective dose to 2 mg/kg by the writhing method. Thirteen related compounds were tested for the activity by intravenous and oral administration to obtain information on the active structure.
Publication DOI: 10.1248/cpb.45.499Journal NLM ID: 0377775Publisher: Pharmaceutical Society Of Japan
Institutions: Faculty of Pharmaceutical Sciences, Chiba University, 1-33 Yayoicho, Inage-ku, Chiba 263, Japan
Methods: 13C NMR, 1H NMR, NMR-2D, IR, FAB-MS, TLC, chemical methods, UV, extraction, pharmacological assay, RP
- Compound ID: 24359
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Caf-(9-4)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet
3,4,8HOPhet = phenylethane-3,4,8-triol;
Caf = caffeic acid |
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Structure type: oligomer
Trivial name: acteoside verbascoside
Compound class: phenylethanoid glycoside
Reference(s) to other database(s): CCSD:
15121, CBank-STR:5112
- Compound ID: 18820
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b-D-Glcp-(1-8)-Subst
Subst = tyrosol = SMILES O{8}CCC1=CC={4}C(O)C=C1 |
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Structure type: monomer
Trivial name: salidroside
Compound class: saponin glycoside, glycoside, phenolic glycoside, flavonol glycoside, phenylethanoid glycoside
Reference(s) to other database(s): CCSD:
49805, CBank-STR:1101
- Compound ID: 22430
Structure type: oligomer
Trivial name: acteoside isomer, isoacteoside, isoverbascoside
Compound class: saponin glycoside, glycoside, phenolic glycoside, phenylethanoid glycoside
- Compound ID: 28023
Structure type: oligomer
; 647 [M+Na]+
Trivial name: acteoside (verbascoside)
Compound class: saponin glycoside
- Compound ID: 28024
Structure type: oligomer
Trivial name: leucosceptoside A, trans-leucosceptoside A
Compound class: saponin glycoside, glycoside, phenolic glycoside, phenylpropanoid glycoside
- Compound ID: 28025
Structure type: oligomer
C31H40O15
Trivial name: martynoside, trans-martynoside
Compound class: saponin glycoside, phenylpropanoid glycoside
- Compound ID: 28026
Structure type: oligomer
Trivial name: jionoside D
Compound class: saponin glycoside
- Compound ID: 28027
Structure type: oligomer
Trivial name: plantamajoside, plantaginin
Compound class: saponin glycoside, glycoside, phenolic glycoside, lignan glycoside, phenylpropanoid glucoside
- Compound ID: 28028
Structure type: monomer
Trivial name: desrhamnosylacteoside
Compound class: saponin glycoside
- Compound ID: 28029
Structure type: oligomer
Trivial name: forsythiaside
Compound class: saponin glycoside, glycoside, phenolic glycoside, lignan glycoside
- Compound ID: 28030
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Caf-(9-4)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-1)-Subst
Subst = phenylethanol = SMILES O{1}CCC1=CC=CC=C1 |
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Structure type: oligomer
Trivial name: jinoside C
Compound class: saponin glycoside
- Compound ID: 28031
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b-D-Glcp-(1-6)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-Subst
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Caf-(9-4)-+
Subst = 2-(3-hydroxyphenyl)-ethanol = SMILES C1={3}C(O)C=CC=C1C{8}CO |
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Structure type: oligomer
Trivial name: echinacoside
Compound class: saponin glycoside
- Compound ID: 28032
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b-D-Galp-(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: purpureaside C
Compound class: saponin glycoside
- Compound ID: 28033
Structure type: oligomer
Trivial name: cistanoside F
Compound class: saponin glycoside, glycoside, phenolic glycoside
- Compound ID: 28034
Structure type: oligomer
Trivial name: decaffeoylacteoside
Compound class: saponin glycoside, glycoside, phenolic glycoside