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Synthesis and anti-tumor activity of pyrazole pyrimidine PI3Kγ/δ inhibitors
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Mao-qing DENG1, 2, Feng-ming ZOU1, 3, Zi-ping QI1, 3, Chun WANG1, 2, Kai-li LONG1, 2, Qing-wang LIU1, 3, Ao-li WANG1, 3, Jing LIU1, 2, 3, *, Xiao-fei LIANG1, 2, 3, *
Acta Pharmaceutica Sinica | 2024, 59(7) : 2041 - 2052
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Acta Pharmaceutica Sinica | 2024, 59(7): 2041-2052
Original Articles
Synthesis and anti-tumor activity of pyrazole pyrimidine PI3Kγ/δ inhibitors
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Mao-qing DENG1, 2, Feng-ming ZOU1, 3, Zi-ping QI1, 3, Chun WANG1, 2, Kai-li LONG1, 2, Qing-wang LIU1, 3, Ao-li WANG1, 3, Jing LIU1, 2, 3, *, Xiao-fei LIANG1, 2, 3, *
Affiliations
  • 1. Institute of Health and Medical Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, China
  • 2. University of Science and Technology of China, Hefei 230026, China
  • 3. Hefei Cancer Hospital, Chinese Academy of Sciences, Hefei 230031, China
Published: 2024-07-12 doi: 10.16438/j.0513-4870.2024-0112
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PI3Kγ and PI3Kδ have important regulatory roles in the immune system, and targeting these two subtypes helps to reshape the tumor microenvironment. PI3Kγ and PI3Kδ are potential targets for tumor immunotherapy. In this study, a series of new pyrazolopyrimidine derivatives were designed and synthesized on the basis of our previously reported PI3K inhibitors, resulting in the discovery of compound 16l as a potent and selective PI3Kγ/δ dual inhibitor. Compound 16l demonstrated strong biochemical potencies against PI3Kγ and PI3Kδ with IC50 values of 0.11 and 0.79 nmol·L-1. In cell-based assays, it potently inhibited the PI3Kγ and PI3Kδ mediated Akt S473 phosphorylation with EC50 values of 3 and 7 nmol·L-1. In vivo, compound 16l exhibited acceptable pharmacokinetic properties in Sprague-Dawley (SD) rats and suppressed the tumor growth in a MC38 syngeneic mouse model. The animal experiments were approved by the Animal Ethics Committee of Hefei Institutes of Physical Science, Chinese Academy of Sciences (approval number: DWLL-2000-06). In addition, no appreciable human ether-a-go-go-related gene (hERG) inhibition was observed for compound 16l even at 30 μmol·L-1. These results suggested that compound 16l might be a potential research tool for studying the PI3Kγ/δ mediated signaling pathways.

PI3Kγ  /  PI3Kδ  /  tumor microenvironment  /  pyrazolo pyrimidine  /  anti-tumor
Mao-qing DENG, Feng-ming ZOU, Zi-ping QI, Chun WANG, Kai-li LONG, Qing-wang LIU, Ao-li WANG, Jing LIU, Xiao-fei LIANG. Synthesis and anti-tumor activity of pyrazole pyrimidine PI3Kγ/δ inhibitors[J]. Acta Pharmaceutica Sinica, 2024 , 59 (7) : 2041 -2052 . DOI: 10.16438/j.0513-4870.2024-0112
Year 2024 volume 59 Issue 7
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Article Info
doi: 10.16438/j.0513-4870.2024-0112
  • Receive Date:2024-02-03
  • Online Date:2025-11-26
  • Published:2024-07-12
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  • Received:2024-02-03
  • Revised:2024-03-14
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Affiliations
    1. Institute of Health and Medical Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, China
    2. University of Science and Technology of China, Hefei 230026, China
    3. Hefei Cancer Hospital, Chinese Academy of Sciences, Hefei 230031, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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