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1. (Article ID: 10442)
Kinjo J, Araki K, Fukui K, Higuchi H, Ikeda T, Nohara T, Ida Y, Takemoto N, Miyakoshi M, Shoji J
Six new triterpenoidal glycosides including two new sapogenols from Albizziae Cortex. V
Chemical and Pharmaceutical Bulletin 40(12) (1992)
3269-3273
Six new triterpenoid glycosides called julibrosides A1-A4,B1 and C1 were isolated from Albizziae Cortex, the dried stem bark of Albizzia julibrissin DURAZZ. Their structures were determined based on spectral and chemical evidence. Julibrosides B1 and C1 had new sapogenols, designated julibrogenin B and C, respectively, while julibrosides A3 included N-acetyl-D-glucosamine as a sugar component.
N-acetyl-d-glucosamine, Leguminosae, oleanene glycoside, Albizziae Cortex, Albizzia julibrissin, oleanene sapogenol, julibrogenin, julibroside
Publication DOI: 10.1248/cpb.40.3269Journal NLM ID: 0377775WWW link: http://ci.nii.ac.jp/naid/110003629729Publisher: Pharmaceutical Society Of Japan
Institutions: School of Pharmaceutical Sciences, Showa University, Japan, Faculty of Pharmaceutical Sciences, Kumamoto University, Japan
Methods: 13C NMR, 1H NMR, EI-MS, gel filtration, IR, FAB-MS, TLC, methylation analysis, NaBH4 reduction, acetylation analysis, saponification
The publication contains the following compound(s):
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2. (Article ID: 10975)
Jia Z, Koike K, Nikaido T, Ohmoto T
Two novel triterpenoid pentasaccharides with an unusual glycosyl glycerol side chain from Ardisia crenata
Tetrahedron 50 (1994)
11853-11864
Two novel triterpenoid pentasaccharides, ardisicrenosides E and F, were isolated from the roots of Ardisia crenata. They are the first examples of a triterpenoid glycoside hybridized with a glycosyl glycerol. Their structures were mainly established on the basis of high field NMR studies. In addition, molecular mechanics and dynamics calculation studies showed that the lack of 13C glycosylation shifts in the Rhamα1→2G′lcβ and G′lcβ1→4Araα fragments in ardisicrenoids E could be correlated with the distortion of the corresponding torsion angles. Both compounds exhibited moderate inhibitory activity on cAMP phosphodiesterase.
Publication DOI: 10.1016/S0040-4020(01)89300-5Journal NLM ID: 2984170RPublisher: Pergamon Press
Institutions: Department of Pharmacognosy, School of Pharmaceutical Sciences, Toho University, Chiba, Japan
Methods: 13C NMR, 1H NMR, EI-MS, IR, FAB-MS, TLC, acid hydrolysis, GLC, HPLC, biological assay
The publication contains the following compound(s):
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3. (Article ID: 10977)
Habermehl GG
Poisonous plants of Brazil
Toxicon 32 (1994)
143-156
Poisonous plants are a serious problem for cattle breeding in Latin America. Owing to the extensive pastural agriculture it is not possible to exterminate such plants. Apart from the considerable financial loss to individual farmers and the national economy owing to dead animals, there is the important question of how far the meat and milk of chronically poisoned animals are a health risk for humans. The toxins of the most important toxic plants from Brazil are described.
NCBI PubMed ID: 8153954Publication DOI: 10.1016/0041-0101(94)90103-1Journal NLM ID: 1307333Publisher: Pergamon Press for International Society On Toxinology
Institutions: Department of Chemistry, Veterinary University, Hannover, F.R.G
The publication contains the following compound(s):
- Compound ID: 27365
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b-D-Manp-(1-6)-a-D-Glcp-(1-3)-Subst4Me7Me
Subst = 1,3,4,7-tetrahydroxyxanthone = SMILES O=C1C2=C(OC3=C1C={7}C(O)C=C3){4}C(O)={3}C(O)C={1}C2O |
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Structure type: oligomer
Compound class: glycoside
Reference(s) to other database(s): CCSD:
50716, CBank-STR:4414
- Compound ID: 27366
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavanone glycoside
Reference(s) to other database(s): CCSD:
50717, CBank-STR:8207
- Compound ID: 27367
|
b-D-Glcp-(1-3)-+
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b-D-Xylp-(1-3)-+ |
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b-D-Glcf-(1-2)-b-D-Xylp-(1-4)-b-L-Rhap-(1-4)-b-D-Xylp-(1-28)-Subst
Subst = medicagenic acid = SMILES CC1(C)CC[C@]2({28}C(O)=O)CC[C@@]3(C)[C@]4(C)CC[C@@]5([H])[C@@]({23}C(O)=O)(C){3}[C@@H](O){2}[C@@H](O)C[C@]5(C)[C@@]4([H])CC=C3[C@]2([H])C1 |
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Structure type: oligomer
Compound class: glycoside
Reference(s) to other database(s): CCSD:
50718, CBank-STR:13219
- Compound ID: 27368
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b-D-Glcp-(1-3)-+
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b-L-Rhap-(1-2)-b-L-Rhap-(1-4)-+ |
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b-D-Xylf-(1-2)-b-D-Xylp-(1-3)-b-D-Xylp-(1-28)-Subst
Subst = 16α-hydroxymedicagenic acid = SMILES C[C@@]1({23}C(O)=O){3}[C@@H](O){2}[C@@H](O)C[C@]2(C)[C@@]3([H])CC=C4[C@]5([H])CC(C)(C)CC[C@@]({28}C(O)=O)5{16}[C@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Compound class: glycoside
Reference(s) to other database(s): CCSD:
50719, CBank-STR:14659
- Compound ID: 20822
Structure type: oligomer
C27H30O16
Trivial name: rutin, rutoside, rutin, quercetin rutinoside, rutoside, quercetin 3-O-rutinose, quercetin-3-O-rutinoside, quercetin 3-O-rutinoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
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