Resultats de la cerca - Krishnapriya Chinnaswamy
- Mostrar 1 - 10 resultats de 10
-
1
-
2
Discovery of Highly Potent and Efficient PROTAC Degraders of Androgen Receptor (AR) by Employing Weak Binding Affinity VHL E3 Ligase Ligands per Xin Han, Lijie Zhao, Weiguo Xiang, Chong Qin, Bukeyan Miao, Tianfeng Xu, Mi Wang, Chao‐Yie Yang, Krishnapriya Chinnaswamy, Jeanne A. Stuckey, Shaomeng Wang
Publicat 2019Artigo -
3
Discovery of M-808 as a Highly Potent, Covalent, Small-Molecule Inhibitor of the Menin–MLL Interaction with Strong <i>In Vivo</i> Antitumor Activity per Shilin Xu, Angelo Aguilar, Liyue Huang, Tianfeng Xu, Ke Zheng, Donna McEachern, Sally Przybranowski, C.L. Foster, Kaitlin P. Zawacki, Zhaomin Liu, Krishnapriya Chinnaswamy, Jeanne A. Stuckey, Shaomeng Wang
Publicat 2020Artigo -
4
SD-91 as A Potent and Selective STAT3 Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression per Haibin Zhou, Longchuan Bai, Renqi Xu, Donna McEachern, Krishnapriya Chinnaswamy, Ruiting Li, Bo Wen, Mi Wang, Chao‐Yie Yang, Jennifer L. Meagher, Duxin Sun, Jeanne A. Stuckey, Shaomeng Wang
Publicat 2021Artigo -
5
High-Affinity Peptidomimetic Inhibitors of the DCN1-UBC12 Protein–Protein Interaction per Haibin Zhou, Weihua Zhou, Bing Zhou, Liu Liu, Ting‐Rong Chern, Krishnapriya Chinnaswamy, Jianfeng Lü, Denzil Bernard, Chao‐Yie Yang, Shasha Li, Mi Wang, Jeanne A. Stuckey, Yi Sun, Shaomeng Wang
Publicat 2018Artigo -
6
A potent small-molecule inhibitor of the DCN1-UBC12 interaction that selectively blocks cullin 3 neddylation per Haibin Zhou, Jianfeng Lü, Liu Liu, Denzil Bernard, Chao-Yie Yang, Ester Fernández‐Salas, Krishnapriya Chinnaswamy, Stephanie Danielle Layton, Jeanne A. Stuckey, Qing Yu, Weihua Zhou, Zhen‐Qiang Pan, Yi Sun, Shaomeng Wang
Publicat 2017Artigo -
7
Mechanistic evaluation and transcriptional signature of a glutathione S-transferase omega 1 inhibitor per Kavya Ramkumar, Soma Samanta, Anahita Kyani, Suhui Yang, Shuzo Tamura, Elizabeth K. Ziemke, Jeanne A. Stuckey, Si Li, Krishnapriya Chinnaswamy, Hiroyuki Otake, Bikash Debnath, V. N. Yarovenko, Judith S. Sebolt‐Leopold, Mats Ljungman, Nouri Neamati
Publicat 2016Artigo -
8
Design of the First‐in‐Class, Highly Potent Irreversible Inhibitor Targeting the Menin‐MLL Protein–Protein Interaction per Shilin Xu, Angelo Aguilar, Tianfeng Xu, Ke Zheng, Liyue Huang, Jeanne A. Stuckey, Krishnapriya Chinnaswamy, Denzil Bernard, Ester Fernández‐Salas, Liu Liu, Mi Wang, Donna McEachern, Sally Przybranowski, C.L. Foster, Shaomeng Wang
Publicat 2017Artigo -
9
A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo per Longchuan Bai, Haibin Zhou, Renqi Xu, Yujun Zhao, Krishnapriya Chinnaswamy, Donna McEachern, Jianyong Chen, Chao‐Yie Yang, Zhaomin Liu, Mi Wang, Liu Liu, Hui Jiang, Bo Wen, Praveen Kumar, Jennifer L. Meagher, Duxin Sun, Jeanne A. Stuckey, Shaomeng Wang
Publicat 2019Artigo -
10
Structure-Based Discovery of SD-36 as a Potent, Selective, and Efficacious PROTAC Degrader of STAT3 Protein per Haibin Zhou, Longchuan Bai, Renqi Xu, Yujun Zhao, Jianyong Chen, Donna McEachern, Krishnapriya Chinnaswamy, Bo Wen, Lipeng Dai, Praveen Kumar, Chao‐Yie Yang, Zhaomin Liu, Mi Wang, Liu Liu, Jennifer L. Meagher, Yi Han, Duxin Sun, Jeanne A. Stuckey, Shaomeng Wang
Publicat 2019Artigo
Eines de cerca:
Matèries relacionades
Biochemistry
Chemistry
Biology
Gene
Genetics
Cancer research
Ubiquitin
Ubiquitin ligase
Enzyme
In vivo
Medicine
Protein–protein interaction
STAT3
Small molecule
Computational biology
Cullin
NEDD8
Neddylation
Pharmacology
Protein subunit
STAT protein
Stereochemistry
Androgen receptor
Bromodomain
Cancer
Cell biology
Cell culture
Covalent bond
DNA ligase
Epigenetics