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1. (Article ID: 12088)
Choi JS, Kim JE, Kim JI, Cheigh HS, Yokozawa T
A flavonol diglucoside from the leaves of Brassica juncea
Natural Product Sciences 6(4) (2000)
199-200
A flavonol diglucoside was isolated from the leaves of Brassica juncea L. The structure of the compound was elucidated as isorhamnetin 3,7-di-O-β-D-glucopyranoside (1) on the basis of chemical and spectral evidence.
Brassica juncea, Brassicaceae, flavonol diglucoside, isorhamnetin 3, 7-di-O-β-D-glucopyranoside
Journal NLM ID: 9714997Publisher: Seoul, Korea: Korean Society of Pharmacognosy
Institutions: Faculty of Food Science and Biotechnology, Pukyong National University, Pusan, South Korea, Department of Food and Nutrition, Pusan National University, Pusan, South Korea, Research Institute for Wakan-Yaku, Toyama Medical and Pharmaceutical University, Sugitani, Japan
Methods: 13C NMR, 1H NMR, UV, extraction, optical rotation measurement, CC, HR-FAB-MS
The publication contains the following compound(s):
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2. (Article ID: 12356)
Leoni O, Iori R, Palmieri S
Hydrolysis of glucosinolates using nylon-immobilized myrosinase to produce pure bioactive molecules
Biotechnology and Bioengineering 68(6) (2000)
660-664
Bioactive compounds were produced from natural glucosinolates, secondary plant metabolites, using myrosinase (thioglucoside glucohydrolase EC 3.2.3.1) isolated from ripe seeds of Sinapis alba. The enzyme was immobilized on granular nylon 6.6 with the crosslinking technique. Immobilized myrosinase displayed extraordinary operational and storage stability. Using a small thermostatted continuous packed-bed bioreactor, the enzyme activity was unchanged after 15 days of continuous use at 37°C and after >1 year of storage at room temperature. The bioreactor was particularly efficient in producing pure isothiocyanates, but it was less efficient for pure nitrile production.
immobilization, bioreactor, myrosinase, glucosinolates, isothiocyanates, nitriles
The publication contains the following compound(s):
- Compound ID: 32061
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b-D-Glcp1S-(1-2)-Subst
Subst = (1E,4E)-5-(methylsulfinyl)-N-(sulfooxy)pent-4-enimidothioic acid = SMILES S/{2}C(CC/C=C/S(C)=O)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucoraphenin, glucoraphanin
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: 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: 32056
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-N-(sulfooxy)pent-4-enimidothioic acid = SMILES C=CCC/{2}C(S)=N\OS(=O)(O)=O |
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Structure type: monomer
Trivial name: gluconapin
Compound class: glycoside, glucosinolate
- Compound ID: 32057
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-3-hydroxy-N-(sulfooxy)pent-4-enimidothioic acid = SMILES C=CC(O)C/{2}C(S)=N\OS(=O)(O)=O |
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Structure type: monomer
Trivial name: epi-progoitrin, epiprogoitrin, progoitrin
Compound class: glycoside, glucosinolate
- Compound ID: 32058
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-2-phenyl-N-(sulfooxy)ethanimidothioic acid = SMILES S/{2}C(CC1=CC=CC=C1)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucotropaeolin
Compound class: glycoside, glucosinolate
- Compound ID: 32060
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-4-(methylthio)-N-(sulfooxy)butanimidothioic acid = SMILES S/{2}C(CCCSC)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucoerucin
Compound class: glycoside, glucosinolate
- Compound ID: 32062
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-4-(methylsulfonyl)-N-(sulfooxy)butanimidothioic acid = SMILES S/{2}C(CCCS(C)(=O)=O)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucocheirolin
Compound class: glycoside, glucosinolate
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