glucose, (beta-d)-isomer has been researched along with resorcinol in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Matsunami, K; Otsuka, H; Shinzato, T; Takeda, Y; Yamashita, Y | 1 |
| Devlamynck, T; Dijkhuizen, L; Te Poele, EM; Valk, V; van Leeuwen, SS | 1 |
| Ishioka, W; Iwadate, T; Nihei, KI; Oonuki, S | 1 |
| Kodachi, Y; Nihei, KI; Suzuki, M; Tanaka, Y | 1 |
4 other study(ies) available for glucose, (beta-d)-isomer and resorcinol
| Article | Year |
|---|---|
Grevillosides A-F: glucosides of 5-alkylresorcinol derivatives from leaves of Grevillea robusta.
Topics: Glucosides; Magnetic Resonance Spectroscopy; Plant Leaves; Proteaceae; Resorcinols | 2008 |
Catechol glucosides act as donor/acceptor substrates of glucansucrase enzymes of Lactobacillus reuteri.
Topics: Bacterial Proteins; Catechols; Crystallography, X-Ray; Gallic Acid; Glucose; Glucosides; Glycosylation; Glycosyltransferases; Limosilactobacillus reuteri; Oligosaccharides; Pyrogallol; Resorcinols; Sucrose | 2017 |
Resorcinol alkyl glucosides as potent tyrosinase inhibitors.
Topics: Alkylation; Dose-Response Relationship, Drug; Enzyme Inhibitors; Glucosides; Molecular Structure; Monophenol Monooxygenase; Resorcinols; Structure-Activity Relationship | 2019 |
Molecular design of potent, hydrophilic tyrosinase inhibitors based on the natural dihydrooxyresveratrol skeleton.
Topics: Agaricales; Enzyme Inhibitors; Fungal Proteins; Glucosides; Inhibitory Concentration 50; Molecular Structure; Monophenol Monooxygenase; Resorcinols; Resveratrol; Structure-Activity Relationship | 2019 |