Found 3 publications.
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1. (Article ID: 10471)
Sawada H, Miyakoshi M, Isoda S, Ida Y, Shoji J
Saponins from leaves of Acanthopanax sieboldianus
Phytochemistry 34 (1993)
1117-1121
Two new triterpenoid saponins named sieboldianoside A and B were isolated from the leaves of Acanthopanax sieboldianus together with five known triterpenoid saponins, kalopanax-saponins A and B, saponin A, CP3, sapindoside B, and a known flavonol glycoside, kaempferol 3-O-rutinoside. On the basis of chemical and spectral evidence, the structures of the new saponins (sieboldianoside A and B) were concluded to be α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)- β-D-glucopyranosyl esters of hederagenin and oleanolic acid 3-O-β-D- xylopyranosyl(1→3)-α-L-rhamnopyranosyl(1→2)-α-L-arabinopyranosides, respectively.
NCBI PubMed ID: 7764238Journal NLM ID: 0151434Publisher: Elsevier
Institutions: School of Pharmaceutical Sciences, Showa University, Tokyo, Japan
The publication contains the following compound(s):
- Compound ID: 25703
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b-D-Xylp-(1-3)-a-L-Rhap-(1-2)-a-L-Arap-(1-3)-+
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a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Hederagenin |
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Structure type: oligomer
Trivial name: sieboldianoside A
Compound class: saponin glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
30430, CBank-STR:14377
- Compound ID: 25704
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b-D-Xylp-(1-3)-a-L-Rhap-(1-2)-a-L-Arap-(1-3)-+
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a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Oleanolic
Oleanolic = 3β-hydroxyolean-12-en-28-oic acid |
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Structure type: oligomer
Trivial name: sieboldianoside B
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
5528, CBank-STR:14376
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2. (Article ID: 10480)
Lin KY, Daniel JR, Whistler RL
Structure of chia seed polysaccharide exudate
Carbohydrate Polymers 23 (1994)
13-18
Journal NLM ID: 8307156Publisher: Elsevier
The publication contains the following compound(s):
- Compound ID: 25730
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a-D-GlcpA4Me-(1-2)-+
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-4)-b-D-Xylp-(1-4)-a-D-Glcp-(1-4)-b-D-Xylp-(1- |
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Structure type: polymer chemical repeating unit
Reference(s) to other database(s): GTC:G91650XL, CCSD:
30960, CBank-STR:10031
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3. (Article ID: 10481)
Chatterton NJ, Harrison PA, Thornley WR, Bennett JH
Structure of fructan oligomers in cheatgrass (Bromus tectorum L.)
New Phytologist 124 (1993)
389-396
Leaves of field-grown cheatgrass (Bromus tectorum L.) plants were sampled during early spring when day- and night-time temperatures were relatively cool. Fructan oligomers with a degree of polymerization (DP) 3–6 were extracted and purified using gel and anion-exchange chromatography. The structures of 13 cheatgrass fructans were established. They included two trisaccharides [1-kestotriose (1-kestose) and 6-kestotriose (6-kestose)], four tetrasaccharides [(1.1)-kestotetraose (nystose), (1&6)-kestotetraose (bifurcose), (6,1)-kestotetraose and (6,6)-kestotetraose], three pentasaccharides [(1,1&6)-kestopentaose, (1&6,6)-kestopentaose and (6;1&6)-kestopentaose] plus four hexasaccharides [(1,1,1&6)-kestohexaose (1&6,6,6)-kestohexaose, (6;1&6,6)-kestohexaose and (6;1,6&6)-kestohexaose]. All fructans larger then DP 4 contained a branch point. Each member of the dominant series(1&6)-kestotetraose, (1&6,6)-kestopentaose and (1&6,6,6)-kestohexaose, is a branched fructan in which two fructose moieties are linked to the fructose subunit of each sucrose molecule. Thus the dominant series is built upon (1&6)-kestotetraose. Fructans larger than DP 3 with exclusively 2→1- or 2→6-linkages were absent except for a very small amount of (6,6)-kestotetraose. The unique fructan structures synthesized in cheatgrass, wheat and oats illustrate diversity in the enzymology of fructan biosynthesis among grass species.
synthesis, Structures, fructan, degree of polymerization, Bromus
Publication DOI: 10.1111/j.1469-8137.1993.tb03829.xJournal NLM ID: 9882884Publisher: Blackwell Publishing
Institutions: USDA Agricultural Research Service, Forage and Range Research Laboratory, Utah State University, Logan, UT, U.S.A.
Methods: partial acid hydrolysis, GC-MS, LC, AE-PAD
The publication contains the following compound(s):
- Compound ID: 547
Structure type: oligomer
Trivial name: nystose, inulin, 1,1-kestotetraose
Compound class: fructan
Reference(s) to other database(s): GTC:G60726JL, GlycomeDB:
63, CCSD:
23519, CBank-STR:9595, GenDB:MH445969, US-PT:US2017298332A1
- Compound ID: 21886
Structure type: oligomer
Trivial name: bifurcose, 1&6-kestotetraose
Reference(s) to other database(s): GTC:G53784JZ
- Compound ID: 25447
Structure type: oligomer
Trivial name: 6,6-kestotetraose
Reference(s) to other database(s): GTC:G99966EK
- Compound ID: 25731
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b-D-Fruf-(2-6)-+
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b-D-Fruf-(2-1)-b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 6,1&6-kestopentaose
Reference(s) to other database(s): GTC:G74226ZA, CCSD:
30977, CBank-STR:12507
- Compound ID: 25732
Structure type: oligomer
Trivial name: 6,1-kestotetraose
Reference(s) to other database(s): GTC:G71059QS
- Compound ID: 25733
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b-D-Fruf-(2-6)-+
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b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 1,1&6-kestopentaose
Reference(s) to other database(s): GTC:G69044FD
- Compound ID: 25734
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b-D-Fruf-(2-1)-+
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b-D-Fruf-(2-6)-b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 1&6,6-kestopentaose
Reference(s) to other database(s): GTC:G25082YN
- Compound ID: 25735
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b-D-Fruf-(2-6)-+
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b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 1,1,1&6-kestohexaose
Reference(s) to other database(s): GTC:G14282RK
- Compound ID: 25736
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b-D-Fruf-(2-1)-+
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b-D-Fruf-(2-6)-b-D-Fruf-(2-6)-b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 1&6,6,6-kestohexaose
Reference(s) to other database(s): GTC:G06716AH
- Compound ID: 25737
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b-D-Fruf-(2-1)-+
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b-D-Fruf-(2-6)-b-D-Fruf-(2-6)-b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 6,1&6,6-kestohexaose
Reference(s) to other database(s): GTC:G12469CG, CCSD:
30978, CBank-STR:14587
- Compound ID: 25738
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b-D-Fruf-(2-6)-+
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b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-b-D-Fruf-(2-6)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: 6,1,6&6-kestohexaose
Reference(s) to other database(s): GTC:G49163YR, CCSD:
30979, CBank-STR:14945
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