1. Computer-aided design and synthesis of 3-carbonyl-5-phenyl-1H-pyrazole as highly selective and potent BRAFV600E and CRAF inhibitor. (1st January 2019) Authors: Kim, Jinwoong; Choi, Byeongha; Im, Daseul; Jung, Hoyong; Moon, Hyungwoo; Aman, Waqar; Hah, Jung-Mi Journal: Journal of enzyme inhibition and medicinal chemistry Issue: Volume 34:Number 1(2019) Page Start: 1314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Conformational restriction of a type II FMS inhibitor leading to discovery of 5-methyl-N-(2-aryl-1H-benzo[d]imidazo-5-yl)isoxazole-4-carboxamide analogues as selective FLT3 inhibitors. (1st January 2019) Authors: Im, Daseul; Moon, Hyungwoo; Kim, Jingwoong; Oh, Youri; Jang, Miyoung; Hah, Jung-Mi Journal: Journal of enzyme inhibition and medicinal chemistry Issue: Volume 34:Number 1(2019) Page Start: 1716 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Design, synthesis, and in vitro evaluation of N-(3-(3-alkyl-1H-pyrazol-5-yl) phenyl)-aryl amide for selective RAF inhibition. Issue 4 (15th February 2019) Authors: Jung, Hoyong; Kim, Jinwoong; Im, Daseul; Moon, Hyungwoo; Hah, Jung-Mi Journal: Bioorganic & medicinal chemistry letters Issue: Volume 29:Issue 4(2019) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Discovery of 3-alkyl-5-aryl-1-pyrimidyl-1H-pyrazole derivatives as a novel selective inhibitor scaffold of JNK3. (1st January 2020) Authors: Oh, Youri; Jang, Miyoung; Cho, Hyunwook; Yang, Songyi; Im, Daseul; Moon, Hyungwoo; Hah, Jung-Mi Journal: Journal of enzyme inhibition and medicinal chemistry Issue: Volume 35:Number 1(2020) Page Start: 372 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Discovery of 5-methyl-N-(2-arylquinazolin-7-yl)isoxazole-4-carboxamide analogues as highly selective FLT3 inhibitors. (1st January 2020) Authors: Im, Daseul; Moon, Hyungwoo; Kim, Jinwoong; Oh, Youri; Jang, Miyoung; Hah, Jung-Mi Journal: Journal of enzyme inhibition and medicinal chemistry Issue: Volume 35:Number 1(2020) Page Start: 1110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Discovery of highly selective CRAF inhibitors, 3-carboxamido-2H-indazole-6-arylamide: In silico FBLD design, synthesis and evaluation. Issue 4 (15th February 2016) Authors: Aman, Waqar; Lee, Junghun; Kim, Minjung; Yang, Songyi; Jung, Hoyong; Hah, Jung-Mi Journal: Bioorganic & medicinal chemistry letters Issue: Volume 26:Issue 4(2016) Page Start: 1188 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Discovery of novel 4-aryl-thieno[1, 4]diazepin-2-one derivatives targeting multiple protein kinases as anticancer agents. Issue 8 (1st May 2018) Authors: Lee, Junghun; Jung, Hoyong; Kim, Minjung; Lee, Eunkyu; Im, Daseul; Aman, Waqar; Hah, Jung-Mi Journal: Bioorganic & medicinal chemistry Issue: Volume 26:Issue 8(2018) Page Start: 1628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Discovery of novel 4-aryl-thieno[1, 4]diazepin-2-one derivatives targeting multiple protein kinases as anticancer agents. Issue 8 (1st May 2018) Authors: Lee, Junghun; Jung, Hoyong; Kim, Minjung; Lee, Eunkyu; Im, Daseul; Aman, Waqar; Hah, Jung-Mi Journal: Bioorganic & medicinal chemistry Issue: Volume 26:Issue 8(2018) Page Start: 1628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel scaffold evolution through combinatorial 3D-QSAR model studies of two types of JNK3 inhibitors. Issue 10 (15th May 2017) Authors: Jung, Hoyong; Aman, Waqar; Hah, Jung-Mi Journal: Bioorganic & medicinal chemistry letters Issue: Volume 27:Issue 10(2017) Page Start: 2139 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Rational design and synthesis of 2-(1H-indazol-6-yl)-1H-benzo[d]imidazole derivatives as inhibitors targeting FMS-like tyrosine kinase 3 (FLT3) and its mutants. (31st December 2022) Authors: Im, Daseul; Jun, Joonhong; Baek, Jihyun; Kim, Haejin; Kang, Dahyun; Bae, Hyunah; Cho, Hyunwook; Hah, Jung-Mi Journal: Journal of enzyme inhibition and medicinal chemistry Issue: Volume 37:Number 1(2022) Page Start: 472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗