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抑制剂&激动剂
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TargetMol产品目录中 "non-genotoxic"的结果
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  • 抑制剂&激动剂
    6
    TargetMol | Inhibitors_Agonists
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    TargetMol | Recombinant_Protein
  • 天然产物
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    TargetMol | Natural_Products
  • 4'-Methylacetophenone
    4'-甲基苯乙酮
    T19137122-00-9
    4′-methylacetophenone 是一种香料,普遍存在于食品中的挥发性化合物和某些天然复合物中。
    • ¥ 99
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    TargetMol | Inhibitor Sale
  • 2,5-Dimethyl-3(2H)-furanone
    2,5-二甲基-3(2H)-呋喃酮, 2,5-Dimethyl-2,3-dihydrofuran-3-one
    T2230914400-67-0
    2,5-Dimethyl-3(2H)-furanone (2,5-Dimethyl-2,3-dihydrofuran-3-one) 是一种调味物质,无遗传毒性。
    • ¥ 119
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  • Cyanazine
    氰草津
    T3965721725-46-2
    Cyanazine, a triazine herbicide, is utilized for effective control of a diverse range of grass and broadleaf weeds. It has been scientifically validated as non-genotoxic.
    • ¥ 334
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  • CYP2C19-IN-1
    T63337
    CYP2C19-IN-1 是强效的,无遗传毒性的、无肝脏毒性的 CYP2C19 抑制剂。 CYP2C19-IN-1 能够抑制 RNA 依赖的 RNA 聚合酶 (RdRP) (Ki: 6.16 μM),能够用于研究寨卡病毒 (ZIKV) 感染。
    • ¥ 10600
    10-14周
    规格
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  • Pidnarulex HCl
    T699082101314-20-7
    Pidnarulex HCl is the salt form of CX-5461, a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhibits rRNA synthesis by Pol I in the nucleolus, but does not inhibit mRNA synthesis by RNA Polymerase II (Pol II) and does not inhibit DNA replication or protein synthesis. Inhibition of Pol I results in nucleolar stress and release of ribosomal proteins (RP) from the nucleolus. The RP bind to Mdm2 and liberate p53 to orchestrate apoptosis in cancer cells. CX-5461 demonstrates a favorable preclinical profile, potently and selectively kills cancer cells, demonstrates robust in vivo efficacy in multiple models, and has demonstrated oral bioavailability in multiple species.
    • ¥ 10600
    6-8周
    规格
    数量
  • rk-701
    T735172648855-18-7
    RK-701 是一种G9a 高选择性且非遗传毒性的抑制剂,IC50值为 23-27 nM。RK-701 选择性的上调 HbF、γ- Globin、BGLT3 的表达,下调 H3K9me2 的表达。RK-701 也对 BCL11A 和 ZBTB7A 有抑制作用。
    • ¥ 12800
    8-10周
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