2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one has been researched along with Blood Poisoning in 10 studies
2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one: specific inhibitor of phosphatidylinositol 3-kinase; structure in first source
| Excerpt | Relevance | Reference |
|---|---|---|
| "Sepsis was induced by cecal ligation and puncture (CLP)." | 1.51 | Neuregulin-1β attenuates sepsis-induced diaphragm atrophy by activating the PI3K/Akt signaling pathway. ( Chu, T; Jiang, P; Li, ST; Liu, H; Wu, J, 2019) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 7 (70.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Shang, X | 1 |
| Lin, K | 1 |
| Yu, R | 1 |
| Zhu, P | 1 |
| Zhang, Y | 1 |
| Wang, L | 1 |
| Xu, J | 1 |
| Chen, K | 1 |
| Fan, TT | 1 |
| Feng, XY | 1 |
| Yang, YZ | 1 |
| Gao, F | 1 |
| Liu, Q | 1 |
| Wan, P | 1 |
| Tan, X | 1 |
| Xiang, Y | 1 |
| Tong, H | 1 |
| Yu, M | 1 |
| Wu, J | 1 |
| Liu, H | 1 |
| Chu, T | 1 |
| Jiang, P | 1 |
| Li, ST | 1 |
| Sun, N | 1 |
| Wang, H | 1 |
| Ma, L | 1 |
| Lei, P | 1 |
| Zhang, Q | 1 |
| Zhou, Z | 1 |
| Gengaro, P | 1 |
| Wang, W | 1 |
| Wang, XQ | 1 |
| Li, C | 2 |
| Faubel, S | 1 |
| Rivard, C | 1 |
| Schrier, RW | 1 |
| Jun, MS | 1 |
| Kim, HS | 1 |
| Kim, YM | 1 |
| Kim, HJ | 1 |
| Park, EJ | 1 |
| Lee, JH | 1 |
| Lee, KR | 1 |
| Kim, YS | 1 |
| Chang, KC | 1 |
| Viñuales, C | 1 |
| Gascón, S | 1 |
| Barranquero, C | 1 |
| Osada, J | 1 |
| Rodríguez-Yoldi, MJ | 1 |
| Williams, DL | 1 |
| Ha, T | 1 |
| Ozment-Skelton, T | 1 |
| Kalbfleisch, JH | 1 |
| Preiszner, J | 1 |
| Brooks, L | 1 |
| Breuel, K | 1 |
| Schweitzer, JB | 1 |
| Connelly, L | 1 |
| Madhani, M | 1 |
| Hobbs, AJ | 1 |
10 other studies available for 2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one and Blood Poisoning
| Article | Year |
|---|---|
Resveratrol Protects the Myocardium in Sepsis by Activating the Phosphatidylinositol 3-Kinases (PI3K)/AKT/Mammalian Target of Rapamycin (mTOR) Pathway and Inhibiting the Nuclear Factor-κB (NF-κB) Signaling Pathway.
Topics: Animals; Apoptosis; Cardiomyopathies; China; Chromones; Disease Models, Animal; Heart; Male; Morphol | 2019 |
Downregulation of PI3K-γ in a mouse model of sepsis-induced myocardial dysfunction.
Topics: Animals; Cardiomyopathies; Chromones; Class II Phosphatidylinositol 3-Kinases; Cytokines; Disease Mo | 2017 |
PI3K/AKT and CD40L Signaling Regulate Platelet Activation and Endothelial Cell Damage in Sepsis.
Topics: Animals; CD40 Ligand; Chromones; Endothelial Cells; Humans; Metabolic Networks and Pathways; Morphol | 2018 |
Neuregulin-1β attenuates sepsis-induced diaphragm atrophy by activating the PI3K/Akt signaling pathway.
Topics: Animals; Chromones; Diaphragm; Disease Models, Animal; Humans; Male; Morpholines; Muscle Contraction | 2019 |
Ghrelin attenuates brain injury in septic mice via PI3K/Akt signaling activation.
Topics: Animals; bcl-2-Associated X Protein; Blood-Brain Barrier; Brain Edema; Brain Injuries; Capillary Per | 2016 |
Role of NF-kappaB and PI 3-kinase/Akt in TNF-alpha-induced cytotoxicity in microvascular endothelial cells.
Topics: Animals; Antioxidants; Cell Survival; Cells, Cultured; Chromones; Endothelial Cells; Endotoxemia; En | 2008 |
Ethanol extract of Prunella vulgaris var. lilacina inhibits HMGB1 release by induction of heme oxygenase-1 in LPS-activated RAW 264.7 cells and CLP-induced septic mice.
Topics: Animals; Anthracenes; Cecum; Cell Line; Cell Survival; Chromones; Cyclooxygenase 2; Disease Models, | 2012 |
Inhibitory effect of IL-1β on galactose intestinal absorption in rabbits.
Topics: Animals; Chromones; Cyclic AMP-Dependent Protein Kinases; Galactose; Genistein; In Vitro Techniques; | 2012 |
Modulation of the phosphoinositide 3-kinase pathway alters innate resistance to polymicrobial sepsis.
Topics: Androstadienes; Animals; Apoptosis; beta-Glucans; Cecum; Chromones; Cytokines; Disease Susceptibilit | 2004 |
Resistance to endotoxic shock in endothelial nitric-oxide synthase (eNOS) knock-out mice: a pro-inflammatory role for eNOS-derived no in vivo.
Topics: Animals; Aorta; Blood Pressure; Blotting, Western; Bone Marrow Cells; Cells, Cultured; Chromones; Cy | 2005 |