In the course of our research on the oligoglycosidic constituents of Turkish Astragalus species, we have isolated a number of cycloartane-type triterpene glycosides. The current study examines the immunostimulatory effects of nineteen of these cycloartane-type compounds using a transcription-based bioassay for Nuclear Factor kappa B (NF-κB) activation in a human macrophage/monocyte cell line, THP-1. All compounds were inactive at 100 μg/ml except astragaloside I which increased NF-κB directed luciferase expression to levels about 65% as compared with maximal stimulation by E. coli lipopolysaccharide (LPS) at 10 μg/ml. None of the compounds were active at low dosage levels (0.1 μg/ml) in combination with 50 ng/ml LPS. Astragaloside I also increased mRNA expression of the inflammatory cytokines interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) as measured using reverse transcriptase-polymerase chain reaction (RT)-PCR. Based on these results it is clear that certain structural features are required for immunostimulation of cycloartane-type triterpene glycosides.
- Compound ID: 31306
|
b-D-Glcp-(1-22)-Subst
Subst = macrophyllosaponins aglycon = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]23C[C@]24CC[C@]5(C)C([C@@H](CC{21}[C@H](O){22}C(C)(O)C)C)CC[C@@]5(C)C4{7}[C@@H](O)CC3C1(C)C |
Show graphically |
Structure type: monomer
Trivial name: macrophyllosaponin C
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31307
|
b-D-Xylp-(1-2)-b-D-Xylp-(1-3)-Subst
Subst = macrophyllosaponins aglycon = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]23C[C@]24CC[C@]5(C)C([C@@H](CC{21}[C@H](O){22}C(C)(O)C)C)CC[C@@]5(C)C4{7}[C@@H](O)CC3C1(C)C |
Show graphically |
Structure type: oligomer
Trivial name: macrophyllosaponin D
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 28879
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: astragaloside IV, astragalus saponin AS I, cycloastragenol
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 30252
|
b-D-Glcp-(1-6)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: monomer
Trivial name: brachyoside B
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 31310
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst
Subst = cyclocanthogenin = SMILES C[C@H](CC{24}[C@H](O){25}C(C)(C)O)[C@H]1{16}[C@@H](O)C[C@@]2(C)[C@@H]3C{6}[C@H](O)[C@H]4C(C)(C){3}[C@@H](O)CC[C@@]45C[C@@]35CC[C@]12C |
Show graphically |
Structure type: oligomer
Trivial name: cyclocanthoside E
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31316
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst
Subst = 20,25-epoxy-3β,6α-dihydroxycycloartane-16β,24α-diol = SMILES C[C@@]6(C)O[C@@](C)([C@H]4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C)CC{24}[C@@H]6O |
Show graphically |
Structure type: oligomer
Trivial name: cyclocephaloside I
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 27852
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp2Ac3Ac-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
C41H68O14
Trivial name: astragaloside I, astragaloside I (astrasieversianin IV)
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 27853
|
b-D-Xylp-(1-6)-+
|
b-D-Xylp2Ac3Ac-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
C41H68O14
Trivial name: astrasieversianin II
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 28886
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp2Ac-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: astragaloside II
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 30251
|
b-D-Xylp-(1-3)-+
|
b-D-Glcp-(1-25)-Subst
|
b-D-Glcp-(1-6)-+
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: astragaloside VII
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 31314
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst16Ac
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: trojanoside A
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31315
|
b-D-Glcp-(1-6)-+
|
a-L-Arap-(1-2)-b-D-Xylp-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: trojanoside H
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31305
|
b-D-Xylp-(1-3)-Subst
Subst = macrophyllosaponins aglycon = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]23C[C@]24CC[C@]5(C)C([C@@H](CC{21}[C@H](O){22}C(C)(O)C)C)CC[C@@]5(C)C4{7}[C@@H](O)CC3C1(C)C |
Show graphically |
Structure type: monomer
Trivial name: macrophyllosaponin B
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31308
|
b-D-Glcp-(1-16)-+
|
a-L-Arap-(1-2)-b-D-Xylp-(1-3)-Subst
Subst = cyclocanthogenin = SMILES C[C@H](CC{24}[C@H](O){25}C(C)(C)O)[C@H]1{16}[C@@H](O)C[C@@]2(C)[C@@H]3C{6}[C@H](O)[C@H]4C(C)(C){3}[C@@H](O)CC[C@@]45C[C@@]35CC[C@]12C |
Show graphically |
Structure type: oligomer
Trivial name: askendoside G
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31309
|
b-D-Xylp-(1-3)-+
|
b-D-Glcp-(1-16)-Subst
Subst = cyclocanthogenin = SMILES C[C@H](CC{24}[C@H](O){25}C(C)(C)O)[C@H]1{16}[C@@H](O)C[C@@]2(C)[C@@H]3C{6}[C@H](O)[C@H]4C(C)(C){3}[C@@H](O)CC[C@@]45C[C@@]35CC[C@]12C |
Show graphically |
Structure type: oligomer
Trivial name: cyclocanthoside D
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31311
|
b-D-Glcp-(1-16)-+
|
b-D-Xylp-(1-24)-Subst
|
b-D-Xylp-(1-3)-+
Subst = cyclocanthogenin = SMILES C[C@H](CC{24}[C@H](O){25}C(C)(C)O)[C@H]1{16}[C@@H](O)C[C@@]2(C)[C@@H]3C{6}[C@H](O)[C@H]4C(C)(C){3}[C@@H](O)CC[C@@]45C[C@@]35CC[C@]12C |
Show graphically |
Structure type: oligomer
Trivial name: cephalatoside A
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31312
|
b-D-Xylp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: astrasieversianin X
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31313
|
b-D-Glcp-(1-6)-+
|
b-D-Glcp-(1-2)-b-D-Xylp-(1-3)-Subst
Subst = astramembrangenin = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C3)C43CC[C@]5(C)[C@@H]([C@](C)(O6)CC[C@H]6{25}C(C)(O)C){16}[C@@H](O)C[C@](C)5[C@]4([H])C{6}[C@H](O)[C@@]12[H] |
Show graphically |
Structure type: oligomer
Trivial name: astragaloside VI
Compound class: glycoside, triterpenoid glycoside