| Stearoyl-CoA desaturase-1 mediated cell apoptosis in colorectal cancer by promoting ceramide synthesis L Chen, J Ren, L Yang, Y Li, J Fu, Y Li, Y Tian, F Qiu, Z Liu, Y Qiu Scientific reports 6 (1), 19665, 2016 | 107 | 2016 |
| Design and Synthesis of Potent N-Acylethanolamine-hydrolyzing Acid Amidase (NAAA) Inhibitor as Anti-Inflammatory Compounds Y Li, L Yang, L Chen, C Zhu, R Huang, X Zheng, Y Qiu, J Fu Public Library of Science 7 (8), e43023, 2012 | 59 | 2012 |
| Potential analgesic effects of a novel N-acylethanolamine acid amidase inhibitor F96 through PPAR-α L Yang, L Li, L Chen, Y Li, H Chen, Y Li, G Ji, D Lin, Z Liu, Y Qiu Scientific reports 5 (1), 13565, 2015 | 53 | 2015 |
| Inflammation-restricted anti-inflammatory activities of a N-acylethanolamine acid amidase (NAAA) inhibitor F215 Y Li, P Zhou, H Chen, Q Chen, X Kuang, C Lu, J Ren, Y Qiu Pharmacological Research 132, 7-14, 2018 | 27 | 2018 |
| Identification of highly potent N-acylethanolamine acid amidase (NAAA) inhibitors: Optimization of the terminal phenyl moiety of oxazolidone derivatives Y Li, Q Chen, L Yang, Y Li, Y Zhang, Y Qiu, J Ren, C Lu European journal of medicinal chemistry 139, 214-221, 2017 | 18 | 2017 |
| Design, synthesis, and biological evaluation of oxazolidone derivatives as highly potent N-acylethanolamine acid amidase (NAAA) inhibitors J Ren, Y Li, H Ke, Y Li, L Yang, H Yu, R Huang, C Lu, Y Qiu RSC advances 7 (21), 12455-12463, 2017 | 16 | 2017 |
| Design and synthesis of uracil urea derivatives as potent and selective fatty acid amide hydrolase inhibitors Y Qiu, J Ren, H Ke, Y Zhang, Q Gao, L Yang, C Lu, Y Li RSC advances 7 (37), 22699-22705, 2017 | 10 | 2017 |
| Discovery of uracil derivatives as potent inhibitors of fatty acid amide hydrolase Y Qiu, Y Zhang, Y Li, J Ren Molecules 21 (2), 229, 2016 | 8 | 2016 |
