glucose, (beta-d)-isomer has been researched along with Prostatic Neoplasms, Castration-Resistant in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, L; Geng, H; Wang, DM; Wei, W; Xia, MZ; Xie, DD; Xu, DX; Xu, S; Yu, DX; Zhang, ZH; Zhang, ZQ | 1 |
| Chattopadhyay, N; Konwar, R; Kumar, A; Kumar, R; Kumar, S; Maurya, R; Ramakrishna, E; Saini, KS | 1 |
2 other study(ies) available for glucose, (beta-d)-isomer and Prostatic Neoplasms, Castration-Resistant
| Article | Year |
|---|---|
Total glucosides of paeony inhibits lipopolysaccharide-induced proliferation, migration and invasion in androgen insensitive prostate cancer cells.
Topics: Active Transport, Cell Nucleus; Apoptosis; Cell Line, Tumor; Cell Movement; Cell Nucleus; Cell Proliferation; Enzyme Activation; Glucosides; Humans; Interleukin-6; Interleukin-8; Lipopolysaccharides; Male; Neoplasm Invasiveness; NF-kappa B; p38 Mitogen-Activated Protein Kinases; Paeonia; Prostatic Neoplasms, Castration-Resistant; Signal Transduction; STAT3 Transcription Factor; Up-Regulation | 2017 |
Quercetin-6-C-β-D-glucopyranoside, natural analog of quercetin exhibits anti-prostate cancer activity by inhibiting Akt-mTOR pathway via aryl hydrocarbon receptor.
Topics: Antineoplastic Agents, Phytogenic; Apoptosis; Basic Helix-Loop-Helix Transcription Factors; Binding Sites; Cell Line; Cell Line, Tumor; Cell Survival; Glucosides; Humans; Ligands; Male; Molecular Docking Simulation; Neoplasm Proteins; Prostate; Prostatic Neoplasms, Castration-Resistant; Proto-Oncogene Proteins c-akt; Quercetin; Reactive Oxygen Species; Receptors, Aryl Hydrocarbon; Resting Phase, Cell Cycle; RNA Interference; Signal Transduction; Structural Homology, Protein; TOR Serine-Threonine Kinases | 2015 |