Design, Synthesis, and In Vitro and In Vivo Evaluation of Cereblon Binding Bruton's Tyrosine Kinase (BTK) Degrader CD79b Targeted Antibody-Drug Conjugates

被引:3
作者
Zhang, Alan [1 ]
Seiss, Katherine [2 ]
Laborde, Laurent [3 ]
Palacio-Ramirez, Sebastian [4 ]
Guthy, Daniel [3 ]
Lanter, Mylene [3 ]
Lorber, Julien [5 ]
Vulpetti, Anna [5 ]
Arista, Luca [5 ]
Zoller, Thomas [5 ]
Radimerski, Thomas [3 ]
Thoma, Claudio [3 ]
Hebach, Christina [3 ]
Tschantz, William R. [4 ]
Karpov, Alexei [5 ]
Hollingworth, Gregory J. [5 ]
D'Alessio, Joseph A. [2 ]
Ferretti, Stephane [3 ]
Burger, Matthew T. [1 ]
机构
[1] Novartis Biomed Res, Global Discovery Chem, Cambridge, MA 02139 USA
[2] Novartis Biomed Res, Oncol Biotherapeut, Cambridge, MA 02139 USA
[3] Novartis Biomed Res, Oncol, CH-4002 Basel, Switzerland
[4] Novartis Biomed Res, Novartis Biol Ctr, Cambridge, MA 02139 USA
[5] Novartis Biomed Res, Global Discovery Chem, CH-4002 Basel, Switzerland
关键词
INDUCED PROTEIN-DEGRADATION; MEDIATED DELIVERY; DISCOVERY; LINKERS;
D O I
10.1021/acs.bioconjchem.3c00535
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody-drug conjugates (ADCs) are an established modality that allow for targeted delivery of a potent molecule, or payload, to a desired site of action. ADCs, wherein the payload is a targeted protein degrader, are an emerging area in the field. Herein we describe our efforts of delivering a Bruton's tyrosine kinase (BTK) bifunctional degrader 1 via a CD79b mAb (monoclonal antibody) where the degrader is linked at the ligase binding portion of the payload via a cleavable linker to the mAb. The resulting CD79b ADCs, 3 and 4, exhibit in vitro degradation and cytotoxicity comparable with that of 1, and ADC 3 can achieve more sustained in vivo degradation than intravenously administered 1 with markedly reduced systemic exposure of the payload.
引用
收藏
页码:140 / 146
页数:7
相关论文
共 34 条
  • [1] Alexander M. D., 2017, Patent No. [WO2017/120422A1, 2017120422]
  • [2] Discovery of LOU064 (Remibrutinib), a Potent and Highly Selective Covalent Inhibitor of Bruton's Tyrosine Kinase
    Angst, Daniela
    Gessier, Francois
    Janser, Philipp
    Vulpetti, Anna
    Walchli, Rudolf
    Beerli, Christian
    Littlewood-Evans, Amanda
    Dawson, Janet
    Nuesslein-Hildesheim, Barbara
    Wieczorek, Grazyna
    Gutmann, Sascha
    Scheufler, Clemens
    Hinniger, Alexandra
    Zimmerlin, Alfred
    Funhoff, Enrico G.
    Pulz, Robert
    Cenni, Bruno
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (10) : 5102 - 5118
  • [3] Arista L., 2021, Patent No. [WO2021/053495A1, 2021053495]
  • [4] Arista L., BENZAMIDE DERIVATIVE
  • [5] PROTAC targeted protein degraders: the past is prologue
    Bekes, Miklos
    Langley, David R.
    Crews, Craig M.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (03) : 181 - 200
  • [6] Development of Anti-CD74 Antibody-Drug Conjugates to Target Glucocorticoids to Immune Cells
    Brandish, Philip E.
    Palmieri, Anthony
    Antonenko, Svetlana
    Beaumont, Maribel
    Benso, Lia
    Cancilla, Mark
    Cheng, Mangeng
    Fayadat-Dilman, Laurence
    Feng, Guo
    Figueroa, Isabel
    Firdos, Juhi
    Garbaccio, Robert
    Garvin-Queen, Laura
    Gately, Dennis
    Geda, Prasanthi
    Haines, Christopher
    Hseih, SuChun
    Hodges, Douglas
    Kern, Jeffrey
    Knudsen, Nickolas
    Kwasnjuk, Kristen
    Liang, Linda
    Ma, Huiping
    Manibusan, Anthony
    Miller, Paul L.
    Moy, Lily Y.
    Qu, Yujie
    Shah, Sanjiv
    Shin, John S.
    Stivers, Peter
    Sun, Ying
    Tomazela, Daniela
    Woo, Hyun Chong
    Zaller, Dennis
    Zhang, Shuli
    Zhang, Yiwei
    Zielstorff, Mark
    [J]. BIOCONJUGATE CHEMISTRY, 2018, 29 (07) : 2357 - 2369
  • [7] Ibrutinib versus Ofatumumab in Previously Treated Chronic Lymphoid Leukemia
    Byrd, J. C.
    Brown, J. R.
    O'Brien, S.
    Barrientos, J. C.
    Kay, N. E.
    Reddy, N. M.
    Coutre, S.
    Tam, C. S.
    Mulligan, S. P.
    Jaeger, U.
    Devereux, S.
    Barr, P. M.
    Furman, R. R.
    Kipps, T. J.
    Cymbalista, F.
    Pocock, C.
    Thornton, P.
    Caligaris-Cappio, F.
    Robak, T.
    Delgado, J.
    Schuster, S. J.
    Montillo, M.
    Schuh, A.
    de Vos, S.
    Gill, D.
    Bloor, A.
    Dearden, C.
    Moreno, C.
    Jones, J. J.
    Chu, A. D.
    Fardis, M.
    McGreivy, J.
    Clow, F.
    James, D. F.
    Hillmen, P.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (03) : 213 - 223
  • [8] Protac-Induced Protein Degradation in Drug Discovery: Breaking the Rules or Just Making New Ones?
    Churcher, Ian
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (02) : 444 - 452
  • [9] Bruton tyrosine kinase degradation as a therapeutic strategy for cancer
    Dobrovolsky, Dennis
    Wang, Eric S.
    Morrow, Sara
    Leahy, Catharine
    Faust, Tyler
    Nowak, Radoslaw P.
    Donovan, Katherine A.
    Yang, Guang
    Li, Zhengnian
    Fischer, Eric S.
    Treon, Steven P.
    Weinstock, David M.
    Gray, Nathanael S.
    [J]. BLOOD, 2019, 133 (09) : 952 - 961
  • [10] Molecular Glues for Targeted Protein Degradation: From Serendipity to Rational Discovery
    Dong, Guoqiang
    Ding, Yu
    He, Shipeng
    Sheng, Chunquan
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2021, 64 (15) : 10606 - 10620