References
- Larsson, B.; Svardsudd, K.; Welin, L.; Wilhelmsen, L.; Bjorntorp, P.; Tibblin, G. British Medical J. 1984, 288, 1401. https://doi.org/10.1136/bmj.288.6428.1401
- Isomaa, B.; Almgren, P.; Tuomi, T.; Forsen, B.; Lahti, K.; Nissen, M.; Taskinen, M. R.; Groop, L. Diabetes Care 2001, 24, 683. https://doi.org/10.2337/diacare.24.4.683
- Foster-Schubert, K. E.; Cummings, D. E. Endocrine Reviews 2006, 27, 779. https://doi.org/10.1210/er.2006-0041
- Cooke, D.; Bloom, S. Nature Rev. Drug Discov. 2006, 5, 919. https://doi.org/10.1038/nrd2136
- Bays, H. E. Obes. Res. 2004, 12, 1197. https://doi.org/10.1038/oby.2004.151
- Jain, S.; Saraf, S. Diabetes & Metabolic Syndrome: Clinical Research & Reviews 2010, 4, 48. https://doi.org/10.1016/j.dsx.2008.04.011
- Seely, B. L.; Staubs, P. A.; Reichart, D. R.; Berhanu, P.; Milarski, K. L.; Saltiel, A. R.; Kusari, J.; Olefsky, J. M. Diabetes 1996, 45, 1379. https://doi.org/10.2337/diabetes.45.10.1379
- Zabolotny, J. M.; Haj, F. G.; Kim, Y. B.; Kim, H. J.; Shulman, G. I.; Kim, J. K.; Neel, B. G.; Kahn, B. B. J. Biol. Chem. 2004, 279, 24844. https://doi.org/10.1074/jbc.M310688200
- Kaszubska, W.; Falls, H. D.; Schaefer, V. G.; Haasch, D.; Frost, L.; Hessler, P.; Kroeger, P. E.; White, D. W.; Jirousek, M. R.; Trevillyan, J. M. Mol. Cell. Endocrinol. 2002, 195, 109. https://doi.org/10.1016/S0303-7207(02)00178-8
- Zabolotny, J. M.; Bence-Hanulec, K. K.; Stricker-Krongard, A.; Haj, F.; Wang, Y. P.; Minokoshi, Y.; Kim, Y.-B.; Elmquist, J. K.; Tartaglia, L. A.; Kahn, B. B.; Neel, B. G. Dev. Cell 2002, 2, 489. https://doi.org/10.1016/S1534-5807(02)00148-X
- Elchebly, M.; Payette, P.; Michaliszyn, E.; Cromlish, W.; Collins, S.; Loy, A. L.; Normandin, D.; Cheng, A.; Himms-Hagen, J.; Chan, C.-C.; Ramachandran, C.; Gresser, M. J.; Tremblay, M. L.; Kennedy, B. P. Science 1999, 283, 1544. https://doi.org/10.1126/science.283.5407.1544
- Kafle, B.; Bhattarai, B. R.; Cho, H. Bull. Korean Chem. Soc. 2011, 32, 31. https://doi.org/10.5012/bkcs.2011.32.1.31
- Bhattarai, B. R.; Kafle, B.; Hwang, J.-S.; Ham, S. W.; Lee, K.-H.; Park, H.; Han, I.-O.; Cho, H. Bioorg. Med. Chem. Lett. 2010, 20, 6758. https://doi.org/10.1016/j.bmcl.2010.08.130
- Bhattarai, B. R.; Lee, K.-H.; Cho, H. Bull. Korean Chem. Soc. 2009, 30, 2879. https://doi.org/10.5012/bkcs.2009.30.12.2879
- Bhattarai, B. R.; Kafle, B.; Hwang, J.-S.; Khadka, D.; Lee, S.-M.; Kang, J.-S.; Ham, S. W.; Han, I.-O.; Park, H.; Cho, H. Bioorg. Med. Chem. Lett. 2009, 19, 6161. https://doi.org/10.1016/j.bmcl.2009.09.020
- Bhattarai, B. R.; Shrestha, S.; Ham, S. W.; Lee, K.-H.; Kim, K. R.; Cheon, H. G.; Cho, H. Bioorg. Med. Chem. Lett. 2007, 17, 5357. https://doi.org/10.1016/j.bmcl.2007.08.019
- Kafle, B.; Aher, N. G.; Khadka, D.; Park, H.; Cho, H. Chemistryan Asian J. 2011, 6, 2073. https://doi.org/10.1002/asia.201100154
Cited by
- Thiazolidinone Derivatives as Competitive Inhibitors of Protein Tyrosine Phosphatase 1B (PTP1B) vol.34, pp.4, 2013, https://doi.org/10.5012/bkcs.2013.34.4.1275
- )-ones pp.00094536, 2017, https://doi.org/10.1002/jccs.201700334
- -toluenesulfonate (PPTS) in aqueous medium vol.48, pp.14, 2018, https://doi.org/10.1080/00397911.2018.1473440
- The synthetic and therapeutic expedition of isoxazole and its analogs vol.27, pp.5, 2018, https://doi.org/10.1007/s00044-018-2152-6
- Privileged Structure-based Discovery of Novel 2-Iminothiazoles as Protein Tyrosine Phosphatase 1B Inhibitors vol.34, pp.10, 2012, https://doi.org/10.5012/bkcs.2013.34.10.2861
- Facile Synthesis and Antioxidant Evaluation of 4-Arylmethylideneisoxazol-5(4H)-ones vol.51, pp.6, 2012, https://doi.org/10.1080/00304948.2019.1677993
- 2,2′-((1,4-Dimethoxy-1,4-dioxobutane-2,3-diylidene)bis(azanylylidene))bis(quinoline-3-carboxylic acid) vol.2019, pp.4, 2019, https://doi.org/10.3390/m1093
- Green Three-component Synthesis of Merocyanin Dyes Based on 4- Arylideneisoxazol-5(4H)-ones vol.7, pp.None, 2020, https://doi.org/10.2174/2213346107666200122093906