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1. (Article ID: 10457)
Luo S, Lin LZ, Cordell GA
Saikosaponin derivatives from Bupleurum wenchuanense
Phytochemistry 33 (1993)
1197-1205
From the roots of Bupleurum wenchuanense 14 derivatives of saikosaponin were isolated and identified as 2″-O-β-d-xylopyranosylsaikosaponin b2, 3″,6″-O,O-diacetylsaikosaponin b2, 2″-O-β-d-glucopyranosylsaikosaponin b2, saikosaponin b2, 6″-O-acetylsaikosaponin b2, saikosaponin d, 2″-O-acetylsaikosaponin d, 3″-O-acetylsaikosaponin d, 6″-O-acetylsaikosaponin d, 16-epichikusaikoside, prosaikogenin G, saikosaponin a, 2″-O-acetylsaikosaponin a and 3″-O-acetylsaikosaponin a. The first two compounds are new derivatives of saikosaponin and this is the first isolation of prosaikogenin G from a plant. Their complete 1H and 13C NMR assignments were made by using a combination of 2D NMR techniques (DQF-COSY, HOHAHA, ROESY, HETCOR, HMQC and HMBC). Some of the compounds showed cytotoxic activity against the P-388 cell line.
cytotoxicity, Umbelliferae, Bupleurum wenchuanense, saikosaponin glucosides, 2″-O-β-d-xylopyranosylsaikosaponin b2, 3″, 6″-O, O-diacetylsaikosaponin b2, 2″-O-β-d-glucopyranosylsaikosaponin b2, saikosaponin b2, 6″-O-acetylsaikosaponin b2, saikosaponin d, 2″-O-acetylsaikosaponin d, 3″-O-acetylsaikosaponin d, 6″-O-acetylsaikosaponin d, 16-epichikusaikoside, prosaikogenin G, saikosaponin a, 2″-O-acetylsaikosaponin a, 3″-O-acetylsaikosaponin a
NCBI PubMed ID: 7764030Publication DOI: 10.1016/0031-9422(93)85049-WJournal NLM ID: 0151434Publisher: Elsevier
Institutions: Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois, Chicago, IL, USA
Methods: 13C NMR, 1H NMR, gel filtration, IR, FAB-MS, cytotoxicity assay
The publication contains the following compound(s):
- Compound ID: 23791
|
b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin F = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: saikosaponin a, saikosaponin-a
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
27760, CBank-STR:3093
- Compound ID: 23792
|
b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: saikosaponin d, saikosaponin-d
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
933, CBank-STR:5893
- Compound ID: 23794
|
b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin D = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=CC4=C5CC(C)(C)CC[C@@]({28}CO)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: saikosaponin a, saikosaponin b2
Compound class: saponin glycoside, glycoside, steroid glycoside
Reference(s) to other database(s): CCSD:
26960, CBank-STR:5890
- Compound ID: 24418
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b-D-Glcp3Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 3″-O-acetylsaikosaponin d
Compound class: saponin glycoside
- Compound ID: 24420
|
b-D-Glcp6Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 6″-O-acetylsaikosaponin d
Compound class: saponin glycoside
- Compound ID: 24421
|
b-D-Glcp3Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin F = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 3″-O-acetylsaikosaponin a
Compound class: saponin glycoside
- Compound ID: 24422
|
b-D-Glcp2Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin F = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 2″-O-acetylsaikosaponin a
Compound class: saponin glycoside
- Compound ID: 24429
|
b-D-Glcp6Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin D = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=CC4=C5CC(C)(C)CC[C@@]({28}CO)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 6″-O-acetylsaikosaponin b2
Compound class: saponin glycoside
- Compound ID: 25203
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin D = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=CC4=C5CC(C)(C)CC[C@@]({28}CO)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 2"-O-β"-D-glucopyranosylsaikosaponin-b2 saikosaponin, 2"-O-β-D-glucopyranosylsaikosaponin-b2
Compound class: saponin glycoside, glycoside, steroid glycoside
Reference(s) to other database(s): CCSD:
29774, CBank-STR:9531
- Compound ID: 25624
|
b-D-Xylp-(1-2)-b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin D = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=CC4=C5CC(C)(C)CC[C@@]({28}CO)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
; 912 [M]+
C47H76O17
Trivial name: 2"-O-β-D-xylopyranosylsaikosaponin-b2
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
29773, CBank-STR:9464
- Compound ID: 25625
|
b-D-Glcp3Ac6Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin D = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=CC4=C5CC(C)(C)CC[C@@]({28}CO)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
C46H72O15
Trivial name: 3",6"-O,O-diacetylsaikosaponin b2
Compound class: saponin glycoside
- Compound ID: 25626
|
b-D-Xylp-(1-2)-b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 16-epichikusaikoside
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
29775, CBank-STR:9462
- Compound ID: 25627
|
b-D-Glcp2Ac-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: 2″-O-acetylsaikosaponin d
Compound class: saponin glycoside
- Compound ID: 25628
|
b-D-Fucp-(1-3)-Subst
Subst = saikogenin G = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: prosaikogenin G
Compound class: saponin glycoside
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