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1. (Article ID: 9818)
Seshadri V, Batta AK, Rangaswami S
Structure of two new saponins from Achyranthes aspera
Indian Journal of Chemistry 20 (1981)
773-775
The publication contains the following compound(s):
- Compound ID: 23927
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = olean-12-en-3β,28-diol = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)CC[C@@]({28}CO)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: rivularinin
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
13086, CBank-STR:7618
- Compound ID: 23928
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a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-GlcpA6Me-(1-3)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
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Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
11074, CBank-STR:7653
- Compound ID: 23929
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b-D-Glcp-(1-28)-+
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a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-GlcpA6Me-(1-3)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
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Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
11075, CBank-STR:10799
- Compound ID: 23930
|
b-D-Glcp-(1-28)-+
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-GlcpA-(1-3)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
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Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
11076, CBank-STR:10797
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2. (Article ID: 9913)
Hariharan V, Rangaswami S
Structure of saponins A and B from the seeds of Achyranthes aspera
Phytochemistry 9 (1970)
409-414
The structure of Achyranthes saponin A has been established as α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→4)-β-D-glucuronopyranosyl(1→3)-oleanolic acid (VI) and that of saponin B as the β-D-galactopyranosyl (1→28) ester of saponin a (VII).
Publication DOI: 10.1016/S0031-9422(00)85154-7Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Department of Chemistry, University of Delhi, Delhi, India
Methods: acid hydrolysis, methylation analysis, PC
The publication contains the following compound(s):
- Compound ID: 23927
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = olean-12-en-3β,28-diol = SMILES CC1(C){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)CC[C@@]({28}CO)5CC[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: rivularinin
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
13086, CBank-STR:7618
- Compound ID: 24086
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-GlcpA-(1-3)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
Show graphically |
Structure type: oligomer
Trivial name: rivularinin
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
13089, CBank-STR:7639
- Compound ID: 24087
|
b-D-Galp-(1-28)-+
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-GlcpA-(1-3)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
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Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
30745, CBank-STR:11127
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3. (Article ID: 12326)
Kunert O, Haslinger E, Schmid MG, Reiner J, Bucar F, Mulatu E, Abebe D, Debella A
Three saponins, a steroid, and a flavanol glycoside from Achyrantes aspera
Monatshefte für Chemie 131(2) (2000)
195-204
Three bisdesmosidic saponins, 20-hydroxyecdysone, and quercetin-3-O-β-D-galactoside were isolated from the methanol extract of the aerial parts of Achyranthes aspera L. (Amaranthaceae). Their structures were established on the basis of NMR spectroscopic analysis; the complete 1H and 13C assignments of the compounds were achieved by means of 2D NMR studies.
NMR spectroscopy, structure elucidation, natural products, saponins
Publication DOI: 10.1007/PL00010306Journal NLM ID: 0254164Publisher: Wien, New York: Springer-Verlag
Institutions: Institut für Pharmazeutische Chemie, Universität Graz, Graz, Austria, Ethiopian Health and Nutrition Research Institute, Addis Ababa, Ethiopia, Institut für Pharmakognosie, Universität Graz, Graz, Austria, Laboratory for Organic Chemistry I, University of Bayreuth, Bayreuth, Germany
The publication contains the following compound(s):
- Compound ID: 21989
Structure type: monomer
Trivial name: hyperoside, hyperin, hyperoside, hyperin, baohuoside-II, quercetin 3-galactoside, vulgarsaponin B
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavanone glycoside
Reference(s) to other database(s): CCSD:
49969, CBank-STR:1983
- Compound ID: 30423
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside, flavonol glycoside
- Compound ID: 31534
Structure type: oligomer
Trivial name: chikusetsusaponin IVa, chikusetsusaponin-IVa
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31987
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
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4. (Article ID: 12480)
Michl G, Abebe D, Bucar F, Debella A, Kunert O, Schmid MG, Mulatu E, Haslinger E
New triterpenoid saponins from Achyrantes aspera Linn.
Helvetica Chimica Acta 83(2) (2000)
359-363
Two new bisdesmosidic triterpenoid saponins, i.e. 1 and 2, were isolated, besides the three known saponins 3–5, from the MeOH extract of the aerial parts of Achyranthes aspera Linn. (Amaranthaceae). Their structures were elucidated as β-D-glucopyranosyl 3β-[O-α-L-rhamnopyranosyl-(1→3)-O-β-D-glucopyranuronosyloxy]machaerinate (1) and β-D-glucopyranosyl 3β-[O-β-D-galactopyranosyl-(1→2)-O-α-D-glucopyranuronosyloxy]machaerinate (2) by NMR spectroscopy, including 2D-NMR experiments (machaerinic acid=3β,21β-dihydroxyolean-12-en-28-oic acid). The other saponins were identified as β-D-glucopyranosyl 3β[O-α-L-rhamnopyranosyl-(1→3)-O-β-D-glucopyranuronosyloxy]oleanolate (3), β-D-glucopyranosyl 3-β-[O-β-D-galactopyranosyl-(1→2)-O-β-D-glucopyranuronosyloxy]oleanolate (4), and β-D-glucopyranosyl 3β-[O-β-D-glucopyranuronosyloxy]oleanolate (5) (oleanolic acid=3β-hydroxyolean-12-en-28-oic acid).
oleanolic acid, triterpenoid saponins, machaerinic acid, Achyranthes aspera
Publication DOI: 10.1002/(SICI)1522-2675(20000216)83:2<359::AID-HLCA359>3.0.CO;2-7Journal NLM ID: 2985094RPublisher: Verlag Helvetica Chimica Acta
Institutions: Institut für Pharmazeutische Chemie, Universität Graz, Graz, Austria, Ethiopian Health and Nutrition Research Institute, Addis Ababa, Ethiopia, Institut für Pharmakognosie, Universität Graz, Graz, Austria, Schering A.G. Berlin, Berlin, Germany
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS
The publication contains the following compound(s):
- Compound ID: 30423
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside, flavonol glycoside
- Compound ID: 31534
Structure type: oligomer
Trivial name: chikusetsusaponin IVa, chikusetsusaponin-IVa
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31987
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32380
|
b-D-Glcp-(1-28)-+
|
a-L-Rhap-(1-3)-b-D-GlcpA-(1-3)-Subst
Subst = machaerinic acid = SMILES O{3}[C@H]1CC[C@@]2([C@]3(CC=C4[C@@]5(CC({21}[C@@H](O)C[C@@]5(CC[C@]4([C@@]3(CC[C@@]2([H])C1(C)C)C)C){28}C(O)=O)(C)C)[H])[H])C |
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Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32381
|
b-D-Glcp-(1-28)-+
|
b-D-Galp-(1-3)-b-D-GlcpA-(1-3)-Subst
Subst = machaerinic acid = SMILES O{3}[C@H]1CC[C@@]2([C@]3(CC=C4[C@@]5(CC({21}[C@@H](O)C[C@@]5(CC[C@]4([C@@]3(CC[C@@]2([H])C1(C)C)C)C){28}C(O)=O)(C)C)[H])[H])C |
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Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
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