LBPO.ET03 · 实验与分子治疗 · Late-Breaking
Late-Breaking Research: Experimental and Molecular Therapeutics 3
23 张海报
10 张含 PDF
🕑 Apr 21 2026 2:00PM 📍 Section 53
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LB344
Discovery of CNP200137, a second-generation menin-MLL inhibitor with superior preclinical properties and anti-leukemic activity against acquired resistance
Jin-Hee Park, Seongshick Ryu, Jae-Seon Lee, Shin-Hae Lee, Dohee Oh, Chaehyeon Seong, Yujung Park, Sumin Kim, Eunbin Park, Jiah Kim, An-Na Moon, Heung Sik Hahm, Jinsun Kwon, Jung Beom Son, Ky-Youb Nam, Jeong Hyeok Yoon, Nam Doo Kim, Hwan Geun Choi
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LB345 · PDF
HZ-V055, an oral, highly potent pan-Ras molecular glue inhibitor demonstrated robust potency in Ras Mut cancer models
Yizhe Wu, Bo Feng, Jiangfeng Xie, Peipei Wang, Jinglai Huang, Xiaobei Hu, Gaoya Xu, Yubo Zhou, Jia Li, Xinglu Zhou
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LB346
A first-in-class TAU-1-directed androgen receptor (AR) and AR-V7 degrader recruits DDB1-CUL4-RBX1 E3 ligase to eliminate AR signaling in lethal prostate cancer
Michelle K. Naidoo, Cherie Au, Kiran K. Sahu, Paraskevi Giannakakou
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LB347 · PDF
Discovery and identification of SHR-RAS001: A structurally novel, highly potent tri-complex RAS multi (ON) inhibitor
Xin Li, Feng Shen, Limin Zhang, Bin Gui, Wei Wang, Yong Liu, Yong Bao, Lu Wang, Yixiu Li, Yuchang Mao, Zaiyong Wang, Chunyue Wang, Jun Feng, Min Hu, Feng He
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LB348 · PDF
Small-molecule targeting of p27 enables coordinated CDK2/4/6 inhibition in CDK4/6i-resistant breast cancer
Grace Chen, Carolina Guido, Charles H. Reynolds, Krishna P. Allamneni, Stacy W. Blain
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LB349
Discovery and preclinical characterization of AIG07025, a potent and selective USP1 inhibitor with broad combination potential
Minjoong Kim, Hyerim Yoo, Miyeon Kim, Ho-Jeong Lee, Eok Park, Jinkwan Kim, Jaewoo Kang
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LB350
Discovery and characterization of ABK-EGFR-1, a 4 th generation EGFR C797S Inhibitor with excellent selectivity and brain penetration
Mei Ning, Juan Peng, Wei Guo, Jie Wang, Jie Zhang, Weijia Lu, Manqi Liu, Haiyan Ying, Haibing Deng, Hongping Yu, Yao-chang Xu
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LB351
Discovery of highly selective, orally available small-molecule DDR1 inhibitors that reprogram the collagen-DDR1 tumor microenvironment
Jungwook Chin, Sun Jun Park, Su-Jeong Lee, Jong-Hyun Park, Jun Young Hong
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LB352
First in class hSSB2 activator as a dual therapeutic strategy for overcoming RAS/MAPK inhibitor resistance while protecting normal epithelia in aggressive cancers
Elizabeth M. Singer, Rishi M. Chugh, Payel Bhanja, Julian P. Whitelegge, William H. McBride, Jesus Rodriguez, Anusha Ravisankar, Mandeep Kumari, Andrew John Norris, Subhrajit Saha
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LB353 · PDF
NPP-2-21: A rationally designed prodrug of a UBA1 inhibitor with improved pharmacologic properties and antitumor activity
Yi Bao, Pengpeng Niu, Ke Ding, Arul M. Chinnaiyan
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LB354
Pharmacologic TSC2 inhibition sensitizes acute myeloid leukemia to proteasome inhibition via mTORC1 mediated mitochondrial catastrophe
Shakti Pattanayak, Boaz Tirosh, Omid Hajihassani, Jordan M. Winter, Kelsey H Fisher-Wellman, Leif A Eriksson
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LB355
ICP-B794, a B7H3-targeting ADC with a novel linker-payload, demonstrated superior anti-tumor activity and large therapeutic window in preclinical studies
Dongliang Mo, Yingxiang Gao, Xiaoyan Wang, Yuan Qian, Hongjuan Zhang, Yingrui Han, Richard Liu, Junjian Liu, Charles Wang, Xiangyang Chen, Bin Zhang
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LB357 · PDF
Preclinical evaluation of ARTS-876, an AKR1C3-activated prodrug targeting KEAP1/NFE2L2-mutant NSCLC
Cong Zhu, Jiaqi Liang, Xiaozhi Yang, Yin Pan, Wenheng Liang, Xiaobin Zhang, Nathan Schomer, Xiang Zhai, Lina Gu, Qing Sheng, Yaoyu Chen, Fang Li
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LB358 · PDF
BPI-585771: A novel, potent pan-KRAS degrader with potent in vitro and in vivo efficacy in KRAS-driven tumors
Zhengqing Li, Renqi Xu, Yanju Liu, Jiayu Zhao, Ying Zhao, Tianyi Ma, Tao Zhang, Bo Yan, Liang Chen, Jing Guo, Cheng Yang, Han Han, Xiaoyun Liu, Haibo Chen, Quan Zhou, Hong Lan, Li Mao, Lieming Ding
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LB359
The Bcl-xL specific PROTAC, DT2216, increases the sensitivity to target therapy of preclinical tumor models from different origin
Giulia Gentile, Elisabetta Valentini, Marta Di Martile, Simona D'Aguanno, Matteo Brignone, Adriana Maria Di Stefano, Marica Di Caprio, Elisa Melucci, Claudio Botti, Fabio Pelle, Arianna Ortolano, Luigi Fattore, Rita Mancini, Gennaro Ciliberto, Dante Rotili, Michela Chiappa, Giovanna Damia, Donatella Del Bufalo
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LB360 · PDF
Targeted degradation of p300 and CBP via antibody-drug conjugate in prostate cancer cells
Fabiola Shelton, Yongqin Wan, Stephen Fuhs, Jocelyn Cheung, Sergio Briones, Gabrielle Cauvi, Hui Qin Wang, Carie Jackson, Bei Chen, Wenqi Gao, Xiaodong Liu, Donnie Delarosa, Eric Peters, Analisa Benedetto, De Shon Hall, Sandra Gao, Julian Wong, John Taraszka, Glenn Federe, John Walker, Saravanan Parthasarathy, Charles Cho, John Hoerter, Jacob R. Haling
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LB361
Selective degradation of a novel kinesin as a potential therapeutic strategy addressing high-risk extrachromosomal DNA (ecDNA) positive cancers, including breast cancer
Deepti Wilkinson, Frederick A. Derheimer, Ardalan Adreshi, Joan Chen, Yuan Chien, Cory DuPai, Rachel Elsdon, Ryan J. Hansen, Kimberly Johnson, Shailaja Kasibhatla, Laura Layman, Zhengke Li, Ronghua Li, Debbie Liao, Taylor Loe, Jacques Mauger, Jafar Moininazeri, Ben Norman, Anne Marie Pferdekamper, Joshua Plum, Casey Sarkissian, Dave Solis, Auzon Steffy, Huikai Sun, Yen Truong, Julie Wiese, Anthony B. Pinkerton, Christian A. Hassig
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LB362 · PDF
P65-047, a novel TEAD degrader, overcomes KRAS inhibitor resistance through Hippo pathway disruption in NSCLC
Rajiv Sawant, Matthis Geitmann, Per Källblad, Samrat T. Kundu, Sofia Garza, Don L. Gibbons, Konrad Koehler, Peter Brandt
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LB363
Discovery and characterization of TXN-A: A first-in-class, orally bioavailable ULK1 degrader with high selectivity and potency for TNBC treatment
Yo Han Hong, Jung-eun Park, Jiah Lim, Yong-Chang Kim, Jun Young Choi, Ye Jin Kim, Young Hoon Choi, Hye Jung Park, Hee Jin Jeong, Chang Won Min, Eunmyong Lee, Hong Jun Kang, Hyouk Woo Lee, Sungjoon Kim, Chan Sun Park
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LB364
TOP1-DNA protein complex as a predictive biomarker for NKTR-102/Rucaparib combination therapy in PARP-inhibitor resistant ovarian cancer
Annapoorna Venkatachalam, Caroline C. Nitschmann, Karen S. Flatten, Rachel Hurley, Xiaonan Hou, Cristina Correia, Paula A. Schenider, Krista Goergen, Matthew Maurer, Ethan P. Heinzen, Ann L. Oberg, S. John Weroha, Paul Haluska, Scott H. Kaufmann, Elizabeth M. Swisher
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LB365 · PDF
Mechanistic and early clinical characterization of VRN101099, a selective HER2 inhibitor with receptor degradation activity
Jun-Young Park, Jihye Yoo, Rasha Cosman, Jee Hung Kim, Christopher Steer, Jieun Lee, Yeon Hee Park, Seock-ah Im, Sun Young Rha, Jee Hyun Kim, Kyung Hae Jung
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LB366 · PDF
Zidesamtinib has differentiated preclinical brain penetrance and intracranial activity compared to other ROS1 inhibitors
Anupong Tangpeerachaikul, Joshua C. Horan, Henry E. Pelish
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LB367
Novel non saccharide glycosaminoglycan mimetic inhibit colorectal cancer stem cells by selectively targeting key tyrosine kinase receptors.
Shoja M. Haneefa, Bharath Villuri, Rio Boothello, Priyanka Mishra, Umesh R. Desai, Bhaumik Patel
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