Found 4 publications.
Displayed publications from 1 to 4
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 8504)
Tanaka M, Yoshimura M, Suto M, Yokota A, Asano K, Sukara E, Tomita F
Production of lepidimoide by an endophytic fungus from polysaccharide extracted from Abelmoschus sp.: identification of the product and the organism producing it
Journal of Bioscience and Bioengineering 93(6) (2002)
531-536
A highly potent allelopathic factor, lepidimoide, was initially extracted from mucilage of germinated cress seeds. Polysaccharide extracted from okra (Abelmoschus esculentum Moench) is considered to have a similar structure to lepidimoide as its repeating unit. We therefore initiated the screening of enzymes capable of degrading okra polysaccharide into lepidimoide from endophytes. We discovered an endophytic fungal strain AHU9748 isolated from Coleus galeatus, which produced an oligosaccharide having similar properties to lepidimoide on thin layer chromatography. The physico-chemical data from ESI-MS, NMR spectra and other analyses also showed the purified product to be identical to lepidimoide. The strain AHU9748 was identified as a fungus belonging to the coelomycetes, closely related to the genus Colletotrichum, based on morphological characteristics and sequence analysis of the 18S rDNA and ITS region
endophytic fungi, lepidimoide, polysaccharide from okra, microbial degradation, Colletotrichum sp.
NCBI PubMed ID: 16233245Publication DOI: 10.1016/s1389-1723(02)80233-xJournal NLM ID: 100888800Publisher: Osaka, Japan, Amsterdam, The Netherlands: Society for Bioscience and Bioengineering
Correspondence: ftomita

chem.agr.hokudai.ac.jp
Institutions: Laboratory of Applied Microbiology, Graduate School of Agriculture, Hokkaido University, Sapporo, Japan, Laboratory of Microbial Resources and Ecology, Graduate School of Agriculture, Hokkaido University, Sapporo, Japan, R & D Center for Biotechnology, LIPI, Bogor, Indonesia
Methods: 13C NMR, 1H NMR, IR, DNA sequencing, TLC, ESI-MS, HPLC, extraction, CC, cell growth, precipitation, centrifugation
The publication contains the following compound(s):
Expand this publication
Collapse this publication
2. (Article ID: 10039)
Shimizu N, Tomoda M
Carbon-13 nuclear magnetic resonance spectra of alditol-form oligosaccharides having the fundamental structural units of the Malvaceae plant mucilages and a related polysaccharide
Chemical and Pharmaceutical Bulletin 33 (1985)
5539-5542
The carbon-13 nuclear magnetic resonance spectra of five alditol-form oligosaccharides and a polysaccharide having the fundamental structural units of the Malvaceae plant mucilages were measured in aqueous solution and the signals were assigned.
13C NMR, structural unit, Malvaceae, plant mucilage, alditol-form oligosaccharide
Journal NLM ID: 0377775WWW link: http://ci.nii.ac.jp/naid/110003625376Publisher: Pharmaceutical Society Of Japan
Institutions: Kyoritsu College of Pharmacy, Tokyo, Japan
Methods: 13C NMR, gel filtration, acid hydrolysis, NaBH4 reduction
The publication contains the following compound(s):
Expand this publication
Collapse this publication
3. (Article ID: 10193)
Tomoda M, Shimizu N, Gonda R, Kanari M, Yamada H, Hikino H
Antidiabetes drugs. Part 36. Anticomplementary and hypoglycemic activity of Okra and Hibiscus mucilages
Carbohydrate Research 190 (1989)
323-328
NCBI PubMed ID: 2805010Publication DOI: 10.1016/0008-6215(89)84136-9Journal NLM ID: 0043535Publisher: Elsevier
Institutions: Pharmaceutical Institute, Tohoku University, Sendai, Japan, Kyoritsu College of Pharmacy, Tokyo, Japan, Oriental Medicine Research Center of the Kitasato Institute, Tokyo, Japan
Methods: biologic assays
The publication contains the following compound(s):
Expand this publication
Collapse this publication
4. (Article ID: 11477)
Perez GRM, Zavala SMA, Perez GS, Perez GC
Antidiabetic effect of compounds isolated from plants
Phytomedicine 5(1) (1998)
55-75
This review shows some of the compounds isolated and identified from the plants that previously demostrated a hypoglycemic effect. These compounds have been classified in appropiate chemical groups and data are reported on their pharmacological activity, mechanism of action, and other properties. This paper reviews mucilages, glycans, proteins, pectins, flavonoids, steroids and triterpenoids, alkaloids, other nitrogen compounds and miscellaneous substances with hypoglycemic effect.
proteins, chemical structures, Plants, glycans, pectins, steroids, triterpenoids, flavonoids, hypoglycemic compounds, mucilages, alkaloids and other nitrogen compounds
NCBI PubMed ID: 23195700Publication DOI: 10.1016/S0944-7113(98)80060-3Journal NLM ID: 9438794Publisher: Stuttgart: Urban & Fischer Verlag
Institutions: Laboratorio de Investigation de Productos Naturales, Escuela Superior de Ingenieria Quimica e Industrias Extractivas, Mexico, Mexico, Departamento de Sistemas Biologicos Universidad Autonoma Metropolitana-Xochimilco, Mexico, Mexico
The publication contains the following compound(s):
- Compound ID: 29314
Structure type: fragment of a bigger structure
Trivial name: mucilage
- Compound ID: 29318
|
/Variants 0/-b-D-Glcp
/Variants 0/ is:
Subst2-(3-1)-
OR (exclusively)
Subst1-(3-1)-
Subst1 = β-sitosterol = SMILES O{3}[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@@]2([H])CC[C@@]4(C)[C@]3([H])CC[C@]4([C@@H](C)CC[C@@H](CC)C(C)C)[H];
Subst2 = 5,25-stigmastadienol = SMILES C=C(C)[C@@H](CC[C@H](C)C3CCC4C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]34C)C(C)C |
Show graphically |
Structure type: monomer
Trivial name: sitosterol-D-glucoside, 5,25-stigmastadienol-glucoside
Compound class: glycoside
- Compound ID: 29319
|
b-D-Glcp-(1-5)-Subst
Subst = divicine = SMILES Nc1nc(N){5}c(O)c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: vicine
Compound class: glycoside
- Compound ID: 29321
|
a-L-Rhap-(1-4)-a-L-Rhap-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = (Z)-3-methyl-dodeca-1,10-dien = SMILES C=C{3}C(C)(O)CCCCCC/C=C\C |
Show graphically |
Structure type: oligomer
Compound class: glycoside
- Compound ID: 29315
|
/Variants 0/-Rhap
/Variants 0/ is:
Quercetin-(3-1)-
OR (exclusively)
Kaempferol-(3-1)- |
Show graphically |
Structure type: monomer
Trivial name: quercetin-3-O-rhamnoside, kaempferol-3-O-rhamnoside
Compound class: glycoside
- Compound ID: 29317
Structure type: oligomer
Trivial name: ginsenoside Rg2
Compound class: triterpenoid glycoside
- Compound ID: 29320
Structure type: oligomer
Trivial name: coyolose
Compound class: glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: 1 sec