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British Journal of Pharmacology, ISSN 0007-1188, 06/2012, Volume 166, Issue 3, pp. 1169 - 1182
BACKGROUND AND PURPOSE Inflammation is involved in the development and/or progression of many diseases including diabetic complications. Investigations on... 
6‐bis(2‐(trifluoromethyl)benzylidene)cyclohexanone | macrophage | (2E; 6E)‐2 | NF‐κB | anti‐inflammation | diabetic nephropathy | NF-κB | anti-inflammation | (2E; 6E)-2 | 6-bis(2-(trifluoromethyl)benzylidene)cyclohexanone | 6E)-2 | ALPHA | CYTOKINE | NEPHROPATHY | IN-VITRO | 2E | NF-?B | MONO-CARBONYL ANALOGS | PATHWAY | ENDOTHELIAL-CELLS | DISEASE | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | NF-KAPPA-B | Curcumin - analogs & derivatives | Diabetes Mellitus, Experimental - drug therapy | Diabetic Nephropathies - enzymology | Cyclohexanones - chemistry | Diabetes Mellitus, Experimental - enzymology | Body Weight - drug effects | Male | Curcumin - administration & dosage | Benzylidene Compounds - chemistry | Diabetic Nephropathies - immunology | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Glucose - administration & dosage | Cell Movement - immunology | Dose-Response Relationship, Drug | Cyclohexanones - therapeutic use | Diabetes Mellitus, Experimental - complications | Cell Culture Techniques | Diabetic Nephropathies - prevention & control | Macrophages, Peritoneal - drug effects | Real-Time Polymerase Chain Reaction | Cytokines - blood | Cytokines - immunology | Diabetic Nephropathies - pathology | Blood Glucose - analysis | Curcumin - therapeutic use | Mice, Inbred C57BL | Curcumin - pharmacology | Macrophages, Peritoneal - immunology | Rats | Cyclohexanones - administration & dosage | Cyclohexanones - pharmacology | Rats, Sprague-Dawley | Blotting, Western | Cell Movement - drug effects | Organ Size - drug effects | Animals | Benzylidene Compounds - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Benzylidene Compounds - therapeutic use | Anti-Inflammatory Agents, Non-Steroidal - administration & dosage | Fibrosis | Benzylidene Compounds - administration & dosage | Diabetes Mellitus, Experimental - pathology | Mice | Research Papers
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2017, Volume 58, Issue 23, pp. 2284 - 2289
[Display omitted] •The synthesis of one advanced intermediate is proposed.•The hydrogenation of the crude cardanol-cardol mixture gave the corresponding... 
Cardanol | Synthesis | CNSL | Cyclohexanone
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 03/2011, Volume 133, Issue 8, pp. 2362 - 2365
Journal Article
天津大学学报:英文版, ISSN 1006-4982, 2017, Volume 23, Issue 3, pp. 230 - 236
Titanium silicalite (TS-1) without and with extra-framework titanium have been prepared and TiO2 is also prepared under the same conditions. All the samples... 
oxime;TiO2 | TS-1;Cyclohexanone;Ammoximation;Cyclohexanone | Ammoximation | TiO | Cyclohexanone | Cyclohexanone oxime | TS-1
Journal Article
Chemical Communications, ISSN 1359-7345, 2017, Volume 53, Issue 38, pp. 5267 - 5270
In the presence of a Ni-Mg-Al layered triple hydroxide-supported Pd catalyst, the acceptorless dehydrogenative aromatization of a wide range of... 
Phenols | Hydrogen storage | Cyclohexanone | Catalysts | Aniline | Dehydrogenation
Journal Article
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 02/2014, Volume 18, Issue 2, pp. 231 - 241
A range of in vitro, experimental and clinical intervention studies have implicated an important role for hyperglycaemia‐induced activation of the... 
mitogen‐activated protein kinases | (2E,6E)‐2,6‐bis(2‐(trifluoromethyl)benzylidene)cyclohexanone | angiotensin converting enzyme | renin‐angiotensin system | diabetic nephropathy | Diabetic nephropathy | (2E,6E)-2,6-bis(2-(trifluoromethyl)benzylidene)cyclohexanone | Renin-angiotensin system | Angiotensin converting enzyme | Mitogen-activated protein kinases | SYSTEM | MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATED PROTEIN-KINASE | RECEPTOR BLOCKADE | 6E)-2 | TRANSCRIPTION | INJURY | MESENCHYMAL TRANSITION | ANGIOTENSIN-CONVERTING ENZYME | 6-bis(2-(trifluoromethyl)benzylidene)cyclohexanone | CELL BIOLOGY | 2E | mitogen-activated protein kinases | ENDOTHELIAL-CELLS | HIGH GLUCOSE | GENE-EXPRESSION | renin-angiotensin system | Diabetes Mellitus, Experimental - drug therapy | Angiotensin II - genetics | Kidney - pathology | Streptozocin | Male | Hyperglycemia - drug therapy | Peptidyl-Dipeptidase A - genetics | Kidney - metabolism | Hyperglycemia - chemically induced | Hyperglycemia - pathology | Peptidyl-Dipeptidase A - metabolism | Diabetes Mellitus, Experimental - chemically induced | Diabetes Mellitus, Experimental - metabolism | Diabetic Nephropathies - prevention & control | Diabetic Nephropathies - pathology | Kidney - drug effects | Angiotensin II - metabolism | Signal Transduction | Diabetic Nephropathies - metabolism | Mice, Inbred C57BL | Diabetic Nephropathies - chemically induced | Gene Expression Regulation | Renin-Angiotensin System - genetics | Cyclohexanones - pharmacology | Hyperglycemia - metabolism | Animals | Benzylidene Compounds - pharmacology | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Diabetes Mellitus, Experimental - pathology | Mitogen-Activated Protein Kinases - genetics | Renin-Angiotensin System - drug effects | Mice | Protein Kinase Inhibitors - pharmacology | Mitogen-Activated Protein Kinases - metabolism | Prevention | Glucose metabolism | Hyperglycemia | Blood sugar | Analysis | Diabetic nephropathies | Angiotensin | Genetic research | Development and progression | Mitogens | Phosphotransferases | Phosphorylation | Funding | Activation | Kinases | Macrophages | Inactivation | Experiments | Proteins | Signal transduction | Renin | Cyclohexanone | Peptidyl-dipeptidase A | Curcumin | Angiotensin II | Deactivation | Kidneys | Diabetes mellitus | MAP kinase | Pharmacology | Inflammation | Grants | Gene expression | Chemical compounds | Studies | ACE protein | Signaling | Inhibitors | Nephropathy | Protein kinase | Collagen | Diabetes | Kidney diseases | Original
Journal Article
ChemCatChem, ISSN 1867-3880, 06/2018, Volume 10, Issue 12, pp. 2508 - 2508
The front cover artwork for issue 12/2018 is provided by Xi'an Jiaotong University and Tsinghua University (China). The image illustrates the different... 
Phenols | Hydrogenation | Palladium
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2019, Volume 60, Issue 25, pp. 1653 - 1657
[Display omitted] •Pd(OAc)2-catalyzed orthogonal synthesis of benzoates and cyclohexanones.•Pd(OAc)2-catalyzed one-pot synthesis of... 
Palladium acetate | Orthogonal synthesis | 2-Hydroxybenzoate | Substituted cyclohexanone
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2019, Volume 55, Issue 15, pp. 2198 - 2201
Single mutation at the switch residues F432 (F432I/L) or L435 (L435A/G) efficiently reversed the inherent enantiopreference of WT CHMOAcineto in the... 
Cyclohexanone | Switches | Oxidation | Mutation | Enantiomers | Substrates | Lactones
Journal Article
Catalysis Communications, ISSN 1566-7367, 12/2016, Volume 87, pp. 70 - 73
In this work and in continuation of our strategy for improving the performance of heterogeneous catalysts, the SiO2@GO-OSO3H catalyst was applied as a very... 
ε-Caprolactam | SiO2@GO-OSO3H | Cyclohexanone oxime | Beckmann rearrangement | SiO | @GO-OSO | SALT | ACID | epsilon-Caprolactam | CHEMISTRY, PHYSICAL | CYCLOHEXANONE-OXIME | STRENGTH | WATER
Journal Article
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 04/2017, Volume 27, Issue 7, pp. 1611 - 1615
Journal Article
ChemBioChem, ISSN 1439-4227, 04/2020, Volume 21, Issue 7, pp. 971 - 977
Baeyer–Villiger monooxygenases (BVMOs) are remarkable biocatalysts, but, due to their low stability, their application in industry is hampered. Thus, there is... 
in silico analysis | enzyme stability | enzyme catalysis | monooxygenases | biocatalysis | Enzymes | Stability | Cyclohexanone | E coli | Cyclohexanone monooxygenase | Melt temperature | Bacteria | Industrial applications | Biocatalysts | Substrates
Journal Article