Found 1 publication.
Displayed publication 1
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (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