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Results for "

non-genotoxic

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Natural Products
    1
    TargetMol | Natural_Products
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    1
    TargetMol | Recombinant_Protein
4'-Methylacetophenone
T19137122-00-9
4'-Methylacetophenone can be used as a fragrance material. It is wildly occurred in volatile compounds in food and in some natural complex substances.
  • $29
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TargetMol | Inhibitor Sale
2,5-Dimethyl-3(2H)-furanone
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) is a non-genotoxic flavoring substance [1].
  • $30
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Cyanazine
T3965721725-46-2
Cyanazine is a triazine-class herbicide extensively utilized for the effective control of a wide variety of grass and broadleaf weeds. Cyanazine has been scientifically validated as non-genotoxic and demonstrates both high selectivity and efficacy in agricultural applications, making it a reliable compound in weed management research and environmental toxicology studies.
  • $35
In Stock
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QTY
CYP2C19-IN-1
T63337
CYP2C19-IN-1 is a potent, non-genotoxic, non-hepatotoxic inhibitor of CYP2C19. CYP2C19-IN-1 inhibits RNA-dependent RNA polymerase (RdRP) (Ki: 6.16 μM) and can be used to study Zika virus (ZIKV) infection.
  • $1,520
10-14 weeks
Size
QTY
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.
  • $1,520
6-8 weeks
Size
QTY
RK-701
T735172648855-18-7
RK-701, a highly selective and non-genotoxic G9a inhibitor, exhibits an IC 50 value of 23-27 nM. It selectively up-regulates HbF, γ-Globin, and BGLT3 expression while down-regulating H3K9me2 expression. Additionally, RK-701 inhibits BCL11A and ZBTB7A.
  • $1,820
8-10 weeks
Size
QTY