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1. (Article ID: 10875)
Gagnon H, Tahara SL, Ibrahim RK
Biosynthesis, accumulation and secretion of isoflavonoids during germination and development of white lupin (Lupinus albus L)
Journal of Experimental Botany 46 (1995)
609-616
Journal NLM ID: 9882906Publisher: Oxford University Press
The publication contains the following compound(s):
- Compound ID: 21445
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b-D-Glcp-(1-7)-Subst
Subst = genistein = SMILES O=C1C(C2=CC={54}C(O)C=C2)=COC3=C1{5}C(O)={6}C{7}C(O)={8}C3 |
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Structure type: monomer
Trivial name: genistin, genistein glucoside
Compound class: glycoside, flavonoid glycoside
Reference(s) to other database(s): CCSD:
48436, CBank-STR:1217
- Compound ID: 27068
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b-D-Glcp-(1-7)-Subst
Subst = 2'-hydroxy-genistein = SMILES O=C1C(C2=CC={54}C(O)C={52}C2O)=COC3=C1{5}C(O)=C{7}C(O)=C3 |
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Structure type: monomer
Trivial name: 2'-hydroxygenistein glucoside
Compound class: glycoside, flavonoid glycoside
Reference(s) to other database(s): CCSD:
48437, CBank-STR:1246
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2. (Article ID: 12611)
Rask L, Andréasson E, Ekbom B, Eriksson S, Pontoppidan B, Meijer J
Myrosinase: gene family evolution and herbivore defense in Brassicaceae
Plant Molecular Biology 42(1) (2000)
93-113
Glucosinolates are a category of secondary products present primarily in species of the order Capparales. When tissue is damaged, for example by herbivory, glucosinolates are degraded in a reaction catalyzed by thioglucosidases, denoted myrosinases, also present in these species. Thereby, toxic compounds such as nitriles, isothiocyanates, epithionitriles and thiocyanates are released. The glucosinolate-myrosinase system is generally believed to be part of the plant's defense against insects, and possibly also against pathogens. In this review, the evolution of the system and its impact on the interaction between plants and insects are discussed. Further, data suggesting additional functions in the defense against pathogens and in sulfur metabolism are reviewed.
cyanogenic glucosides, myrosinase, glucosinolates, O-β-glucosidase, plant–insect interaction
NCBI PubMed ID: 10688132Publication DOI: 10.1023/A:1006380021658Journal NLM ID: 9106343Publisher: Dordrecht: Kluwer Academic
Institutions: Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden, Department of Plant Biology, Swedish University of Agricultural Sciences, Uppsala, Sweden, Department of Entomology, Swedish University of Agricultural Sciences, Uppsala, Sweden
The publication contains the following compound(s):
- Compound ID: 31348
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-N-(sulfooxy)but-3-enimidothioic acid = SMILES C=CC/{2}C(S)=N\OS(=O)(O)=O |
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Structure type: monomer
Trivial name: sinigrin
Compound class: glycoside, glucosinolate
- Compound ID: 32059
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-2-(4-hydroxyphenyl)-N-(sulfooxy)ethanimidothioic acid = SMILES S/{2}C(CC1=CC(O)=CC=C1)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: sinalbin
Compound class: glycoside, glucosinolate
- Compound ID: 32538
Structure type: monomer
Trivial name: glucobrassicin
Compound class: glycoside, glucosinolate
- Compound ID: 32540
Structure type: monomer
Trivial name: neoglucobrassicin
Compound class: glycoside, glucosinolate
- Compound ID: 32643
Structure type: monomer
Trivial name: 4-hydroxybrassicin
Compound class: glycoside, glucosinolate
- Compound ID: 32644
Structure type: monomer
Trivial name: gluconasturtiin, gluconasturtin
Compound class: glycoside, glucosinolate
- Compound ID: 32645
Structure type: monomer
Trivial name: glucobarbarin
Compound class: glycoside, glucosinolate
- Compound ID: 32646
Structure type: monomer
Trivial name: glucoraphenin
Compound class: glycoside, glucosinolate
- Compound ID: 32647
Structure type: monomer
Trivial name: gluconapin
Compound class: glycoside, glucosinolate
- Compound ID: 32648
Structure type: monomer
Trivial name: glucobrassicianapin
Compound class: glycoside, glucosinolate
- Compound ID: 32649
Structure type: monomer
Trivial name: progoitrin
Compound class: glycoside, glucosinolate
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