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- The advanced reprocessing of spent nuclear fuel is a potential key to achieve a sustainable nuclear fuel cycle and to tackle the heavy burden of nuclear...39 KB (4,958 words) - 21:54, 31 December 2023
- BMF-219 is an investigational irreversible covalent inhibitor of menin. It is developed by Biomea Fusion for diabetes, lymphoma, leukemia, and multiple...5 KB (196 words) - 15:51, 3 June 2024
- Brigimadlin (BI-907828) is a small molecule MDM2-TP53 inhibitor developed for liposarcoma. "Brigimadlin". pubchem.ncbi.nlm.nih.gov. Rinnenthal, Joerg;...5 KB (337 words) - 07:17, 5 April 2024
- S-309309 is an experimental MGAT2 inhibitor developed as an anti-obesity drug by the Japanese company Shionogi. Phase II trial results are expected in...4 KB (110 words) - 12:44, 4 September 2024
- George Clyde Hale (September 29, 1881 – November 3, 1948) received a patent in 1935 for the explosive ethylenedinitramine (EDNA) which was named Haleite...9 KB (966 words) - 09:52, 27 May 2024
- HEC96719 is a tricyclic farnesoid X receptor agonist developed for non-alcoholic steatohepatitis. Cao, Shengtian; Yang, Xinye; Zhang, Zheng; Wu, Junwen;...5 KB (182 words) - 08:36, 14 September 2024
- Omesdafexor (MET642) is a small-molecule farnesoid X receptor (FXR) agonist developed for nonalcoholic steatohepatitis and colitis. Liu, Xueqing; O'Connell...4 KB (101 words) - 05:46, 7 December 2023
- Rencofilstat (CRV431) is a pan-cyclophilin inhibitor and analog of cyclosporine A developed for nonalcoholic steatohepatitis and hepatocellular carcinoma...6 KB (232 words) - 11:51, 6 January 2024
- Opnurasib (JDQ-443) is a small-molecule covalent KRASG12C inhibitor developed for non-small-cell lung cancer. Weiss, Andreas; Lorthiois, Edwige; Barys...7 KB (412 words) - 21:11, 25 April 2024
- Mezigdomide is a cereblon E3 ligase modulator developed by Bristol Myers Squibb to treat multiple myeloma. Richardson, Paul G.; Trudel, Suzanne; Quach...7 KB (406 words) - 00:39, 18 December 2023
- EDP-305 is a non-bile acid farnesoid X receptor (FXR) agonist developed by Enanta Pharmaceuticals for non-alcoholic fatty liver disease. According to preclinical...5 KB (221 words) - 18:08, 5 January 2024
- ZSP1601 is an experimental pan-phosphodiesterase inhibitor developed by Guangdong Raynovent Biotech for nonalcoholic steatohepatitis. Zhu, Xiaoxue; Wu...4 KB (174 words) - 00:06, 26 September 2024
- SPH3127 is a small-molecule renin inhibitor developed by Shanghai Pharmaceuticals for hypertension and kidney disease. It is believed to be more potent...5 KB (200 words) - 00:18, 1 January 2024
- DA-1241 is an experimental GPR119 receptor agonist developed by the South Korean company Dong-A ST for non-alcoholic steatohepatitis and type 2 diabetes...5 KB (270 words) - 12:53, 5 August 2024
- Denifanstat (TVB-2640) is a small-molecule drug and fatty acid synthase inhibitor. Developed by Sagimet Biosciences, it has been tested in various types...6 KB (310 words) - 12:35, 4 January 2024
- Ninerafaxstat (IMB-1018972 or IMB-101) is a cardiac mitotrope agent investigated by Imbria for diabetic cardiomyopathy, myocardial ischemia, and hypertrophic...4 KB (170 words) - 19:43, 23 September 2024
- Prusogliptin (DBPR108) is an experimental DPP-4 inhibitor developed by CSPC Pharmaceutical Group to treat type 2 diabetes. Xu, Jianping; Ling, Hongwei;...5 KB (268 words) - 22:50, 31 December 2023
- ZED1227 is a transglutaminase 2 (TG2) inhibitor developed by Zedira GmbH for celiac disease and nonalcoholic steatohepatitis. Schuppan, Detlef; Mäki, Markku;...5 KB (168 words) - 03:55, 25 September 2024
- BMS-986278 is an experimental small-molecule drug and lysophosphatidic acid receptor 1 (LPA1) antagonist developed by Bristol Myers Squibb for idiopathic...7 KB (378 words) - 10:10, 3 December 2023
- Verinurad is a selective URAT1 inhibitor developed for gout and heart failure by AstraZeneca. Johansson, Susanne; Han, David; Hunt, Thomas; Björck, Karin;...4 KB (194 words) - 21:41, 31 December 2023