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    • abs47028127A 438079 hydrochloride  899431-18-6
      abs47028127A 438079 hydrochloride 899431-18-6

      A 438079 hydrochloride 899431-18-6 A-438079 hydrochloride is a potent, and selective P2X7 receptor antagonist with pIC50 of 6.9.

      更新時間:2026-01-19型號:abs47028127訪問量:678
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    • abs47028126Regadenoson 313348-27-5
      abs47028126Regadenoson 313348-27-5

      Regadenoson 313348-27-5 Regadenoson is an adenosine derivative and selective A2A adenosine receptor agonist with coronary vasodilating activity.

      更新時間:2026-01-19型號:abs47028126訪問量:581
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    • abs47028125PIK-75 372196-67-3
      abs47028125PIK-75 372196-67-3

      PIK-75 372196-67-3 PIK-75, a DNA-PK and PI3K inhibitor, suppresses DNA-PK(IC50=2 nM), p110α(IC50=5.8 nM) and p110γ(IC50=76 nM).

      更新時間:2026-01-19型號:abs47028125訪問量:609
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    • abs47028123Fruquintinib 1194506-26-7
      abs47028123Fruquintinib 1194506-26-7

      Fruquintinib 1194506-26-7 Fruquintinib (HMPL-013) is a small molecule vascular endothelial growth factor receptors inhibitor.

      更新時間:2026-01-19型號:abs47028123訪問量:587
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    • abs47028122CEP37440 1391712-60-9
      abs47028122CEP37440 1391712-60-9

      CEP37440 1391712-60-9 CEP-37440 is a novel potent and selective Dual FAK/ALK inhibitor with IC50 s of 2.3 nM (FAK) and 120 nM(ALK cellular IC50 in 75% human plasma).

      更新時間:2026-01-19型號:abs47028122訪問量:623
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    • abs47028120MI-2 (Menin-MLL Inhibitor) 1271738-62-5
      abs47028120MI-2 (Menin-MLL Inhibitor) 1271738-62-5

      MI-2 (Menin-MLL Inhibitor) 1271738-62-5 MI-2 (Menin-MLL Inhibitor) is a potent menin-MLL interaction inhibitor with IC50 of 446 nM.

      更新時間:2026-01-19型號:abs47028120訪問量:611
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    • abs47028119HA130 1229652-21-4
      abs47028119HA130 1229652-21-4

      HA130 1229652-21-4 HA130 is a selective ATX (autotaxin) inhibitor with IC50 of 28 nM.

      更新時間:2026-01-19型號:abs47028119訪問量:594
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    • abs47028117KRCA-0008 1472795-20-2
      abs47028117KRCA-0008 1472795-20-2

      KRCA-0008 1472795-20-2 KRCA-0008 is a potent and selective ALK/Ack1 inhibitor with IC50 of 12 nM/4 nM for ALK and Ack1 respectively; displays drug-like properties without hERG liability.

      更新時間:2026-01-19型號:abs47028117訪問量:564
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