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抑制剂&激动剂
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TargetMol产品目录中 "tyrosyl-dna phosphodiesterase 1"的结果
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TargetMol产品目录中 "

tyrosyl-dna phosphodiesterase 1

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  • 抑制剂&激动剂
    7
    TargetMol | Inhibitors_Agonists
  • TDP1 Inhibitor-1
    T131092248702-80-7
    TDP1 Inhibitor-1 is a potent inhibitor of Tyrosyl-DNA Phosphodiesterase 1 (TDP1) (IC50 of 7 μM).
    • ¥ 11700
    6-8周
    规格
    数量
  • Norchlorcyclizine
    C-10, C10, C 10, 1-(4-氯二苯甲基)哌嗪
    T20499303-26-4
    Norchlorcyclizine (C-10) 是一种部分选择性的 NPR-B 抑制剂。它也是人酪氨酰-DNA 磷酸二酯酶 1 的抑制剂。
    • ¥ 99
    In stock
    规格
    数量
    TargetMol | Inhibitor Sale
  • Furamidine
    DB75, NSC 305831
    T1133873819-26-8
    Furamidine is also a selective and cell-permeable protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 of 9.4 μM. Furamidine is selective for PRMT1 over PRMT5, PRMT6, and PRMT4 (CARM1) (IC50s of 166 μM, 283 μM, and >400 μM, respectively). Furamidine (DB75) is abisbenzamidine derivative and an antiparasite agent. Furamidine is a potent, reversible and competitive tyrosyl-DNA phosphodiesterase 1 (TDP-1) inhibitor. Inhibition of TDP-1 by Furamidine is effective both with single- and double-stranded DNA substrates but is slightly stronger with the duplex DNA.
    • ¥ 10600
    6-8周
    规格
    数量
  • CID-7309015
    T252511164457-99-1
    CID-7309015 is a human tyrosyl-DNA phosphodiesterase 1 (TDP1) inhibitor, delayed death of the malarial parasite plasmid, the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1, ROR gamma transcriptiona
    • ¥ 10600
    6-8周
    规格
    数量
  • TDP1 Inhibitor-2
    T62965859142-95-3
    TDP1 Inhibitor-2 是一种 TDP1 (酪氨酰 -DNA 磷酸二酯酶 1) 的有效抑制剂 (IC50: 99 nM)。TDP1 Inhibitor-2 对 SCAN1 (脊髓小脑共济失调综合征伴轴突神经病变) 具有抑制作用 (IC50: 3.5 μM)。
    • ¥ 14900
    6-8周
    规格
    数量
  • NSC109131
    T6989321170-27-4
    NSC109131 is an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1).
    • ¥ 10600
    6-8周
    规格
    数量
  • TX-2552
    T892342446767-14-0
    TX-2552为口服型TDP1 (酪氨酰DNA磷酸二酯酶1) 抑制剂,具备IC50为0.62 μM的活性.该化合物能够提升拓扑替康在小鼠骨髓细胞中的断裂活性,并增强其在Krebs-2腹水瘤模型中的抗肿瘤效果.
    • 待询
    10-14周
    规格
    数量