WO2025026283 - COMPOUND FOR SELECTIVELY DEGRADING SMARCA2/4 AND USE THEREOF

National phase entry is expected:
Publication Number WO/2025/026283
Publication Date 06.02.2025
International Application No. PCT/CN2024/108262
International Filing Date 29.07.2024
Title **
[English] COMPOUND FOR SELECTIVELY DEGRADING SMARCA2/4 AND USE THEREOF
[French] COMPOSÉ POUR DÉGRADER SÉLECTIVEMENT SMARCA2/4 ET SON UTILISATION
[Chinese] 一种选择性降解SMARCA2/4的化合物及其应用
Applicants **
GAN & LEE PHARMACEUTICALS CO., LTD.
Inventors
XU, Fuming
CHEN, Wenmin
LI, Xiaoguang
DING, Yongzheng
ZHOU, Guan
GU, Siyu
Priority Data
202310939545.8   28.07.2023   CN
202410864991.1   01.07.2024   CN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting3209
EPO Filing, Examination, Granting18382
Japan Filing, Examination, Granting2247
South Korea Filing, Examination, Granting2369
USA Filing, Examination, Granting6090
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Total: 32,297

The term for entry into the National Phase has expired. This quotation is for informational purposes only

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Abstract[English] The present disclosure relates to a compound capable of being used as a SMARCA2/4 modulator. Specifically, the compound involved in the present disclosure contains a ligand at one end that binds to an E3 ubiquitin ligase, and contains a ligand at the other end that binds to a target protein (SMARCA2/4), such that the target protein is placed in the vicinity of the ubiquitin ligase, so as to achieve the degradation (or inhibition) of the target protein.[French] La présente divulgation concerne un composé pouvant être utilisé en tant que modulateur de SMARCA2/4. Spécifiquement, le composé impliqué dans la présente divulgation contient un ligand à une extrémité qui se lie à une ubiquitine ligase E3, et contient un ligand à l'autre extrémité qui se lie à une protéine cible (SMARCA2/4), de telle sorte que la protéine cible est placée à proximité de l'ubiquitine ligase, de façon à obtenir la dégradation (ou l'inhibition) de la protéine cible.[Chinese] 本公开涉及可用作SMARCA2/4调节剂的化合物。具体地讲,本公开所涉及到的化合物在一端上含有结合E3泛素连接酶的配体,并且在另一端上含有结合靶蛋白(SMARCA2/4)的配体,使得所述靶蛋白被置于所述泛素连接酶附近,以实现靶蛋白的降解(或抑制)。