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Ciclo celular/Ponto de verificação

Ciclo celular/Ponto de verificação

Os inibidores do ciclo celular/ponto de verificação são compostos que interrompem a progressão normal do ciclo celular, particularmente em pontos de verificação regulatórios chave. Esses inibidores são cruciais para estudar a divisão celular, entender a proliferação de células cancerígenas e desenvolver terapias anticâncer. Ao direcionar fases específicas do ciclo celular, esses inibidores podem induzir a parada do ciclo celular, levando à apoptose ou senescência em células de divisão rápida. Na CymitQuimica, oferecemos uma ampla gama de inibidores de alta qualidade do ciclo celular/ponto de verificação para apoiar sua pesquisa em biologia do câncer, biologia celular e desenvolvimento de medicamentos.

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Foram encontrados 3756 produtos de "Ciclo celular/Ponto de verificação"

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  • WRN inhibitor 13

    CAS:
    WRN inhibitor 13 is an inhibitor of the WRN helicase with a pIC50 value ranging from 6 to 7.
    Fórmula:C16H20N2O5S
    Cor e Forma:Solid
    Peso molecular:352.405
  • DNA polymerase-IN-6

    CAS:
    DNA polymerase-IN-6 (Compound 27) exhibits inhibitory activity against DNA polymerase, with EC50 values of 0.33 µM for HCMV, 1.9 µM for HSV-1, 0.76 µM for HSV-2, and 0.066 µM for EBV.
    Fórmula:C26H28ClFN8O4
    Cor e Forma:Solid
    Peso molecular:571.003
  • Hesperadin hydrochloride


    Hesperadin hydrochloride is an ATP-competitive indolone inhibitor of Aurora A and B, with an IC50 value of 250 nM for Aurora B.
    Fórmula:C29H33ClN4O3S
    Cor e Forma:Solid
    Peso molecular:553.12
  • FR-β ligand 1

    CAS:
    FR-β ligand 1 (III) is a ligand that specifically targets folate receptors, exhibiting antitumor activity, high selectivity, and strong affinity.
    Fórmula:C22H25N5O6
    Cor e Forma:Solid
    Peso molecular:455.46
  • CDK9-IN-13


    CDK9-IN-13 is a potent and selective CDK inhibitor (IC50<3 nM). CDK9-IN-13 has a very short half-life in rodents.
    Fórmula:C27H35N5O2
    Cor e Forma:Solid
    Peso molecular:461.6
  • N-Isobutyryl-2', 3'-acetyl-guanosine

    CAS:
    N-Isobutyryl-2', 3'-acetyl-guanosine is a derivative of guanosine.
    Fórmula:C18H23N5O8
    Cor e Forma:Solid
    Peso molecular:437.404
  • 2'-O-MOE-GMP

    CAS:
    <p>2'-O-MOE-GMP is a nucleotide analogue that can be utilized in the synthesis of oligonucleotides.</p>
    Fórmula:C13H20N5O9P
    Cor e Forma:Solid
    Peso molecular:421.30
  • Mazethramycin

    CAS:
    <p>Mazethramycin is an antitumor antibiotic that exerts its effects by disrupting DNA replication and RNA synthesis within cells. It is utilized in cancer research.</p>
    Fórmula:C17H19N3O4
    Peso molecular:329.35
  • Chk1-IN-5

    CAS:
    Chk1-IN-5 inhibits Chk1, blocking phosphorylation and suppressing colon cancer growth.
    Fórmula:C18H18FN7O2
    Cor e Forma:Solid
    Peso molecular:383.38
  • DYRKs-IN-1 hydrochloride

    CAS:
    DYRKs-IN-1 HCl inhibits DYRK1A (5 nM IC50) & DYRK1B (8 nM IC50) with antitumor properties.
    Fórmula:C30H31Cl2N7O4
    Cor e Forma:Solid
    Peso molecular:624.52
  • CDK7-IN-18

    CAS:
    CDK7-IN-18: potent, pyrimidine-based CDK7 inhibitor with cancer research potential.
    Fórmula:C22H24F3N7OS
    Pureza:99.28%
    Cor e Forma:Solid
    Peso molecular:491.53
  • CDK9-IN-38

    CAS:
    <p>CDK9-IN-38 (compound 14) is a CDK9 inhibitor with IC50 values of 1.2 nM for wild-type CDK9 and 3.3 nM for the L156F mutant. It effectively inhibits tumor growth both in vitro and in vivo.</p>
    Fórmula:C22H23N5O3S
    Cor e Forma:Solid
    Peso molecular:437.515
  • 4,5'-Dimethylangelicin-NHS


    NHS-modified coumarin, 4,5'-Dimethylangelicin-NHS, shows photochemical activity & photosensitivity.
    Fórmula:C21H19NO7S
    Cor e Forma:Solid
    Peso molecular:429.44
  • CHK1-IN-2

    CAS:
    CHK1-IN-2 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 6 nM).
    Fórmula:C20H22N4OS
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:366.48
  • MtTMPK-IN-9


    MtTMPK-IN-9 moderately inhibits MtbTMPK (IC50: 48 μM), has submicromolar Mycobacterium activity, and is non-toxic, aiding tuberculosis research.
    Fórmula:C25H26N6O7
    Cor e Forma:Solid
    Peso molecular:522.51
  • (Rac)-Plevitrexed

    CAS:
    (Rac)-Plevitrexed is a racemate of Plevitrexed. Plevitrexed is an orally active and potent inhibitor of thymidylate synthase (TS).
    Fórmula:C26H25FN8O4
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:532.53
  • FT709

    CAS:
    FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways.
    Fórmula:C23H22N4O7S
    Cor e Forma:Solid
    Peso molecular:498.51
  • CB 30900

    CAS:
    CB30900 is a novel and effective thymidylate synthase inhibitor.
    Fórmula:C31H32FN5O9
    Cor e Forma:Solid
    Peso molecular:637.61
  • CLK1/2-IN-1

    CAS:
    CLK1/2-IN-1 is a CLK1 and CLK2 inhibitor and it also inhibits SRPK1 and SRPK2.
    Fórmula:C21H20F3N7O
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:443.42
  • Ascofuranone

    CAS:
    Ascofuranone is an inhibitor of the ubiquinol oxidase activity of Trypanosoma brucei mitochondrial alternative oxidase (TAO), as well as an inhibitor of HsDHODH
    Fórmula:C23H29ClO5
    Cor e Forma:Solid
    Peso molecular:420.93