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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 3764 produtos de "Ciclo celular/Ponto de verificação"

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  • N6-Methyl-2'-O-(2-methoxyethyl) adenosine


    N6-Methyl-2’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid malignancies.
    Fórmula:C14H21N5O5
    Cor e Forma:Solid
    Peso molecular:339.35
  • Adenosine Dialdehyde (ADOX)

    CAS:
    Adenosine Dialdehyde, a purine analogue, inhibits SAHH (Ki=3.3 nM), and shows strong anti-tumor effects in vivo.
    Fórmula:C10H11N5O4
    Pureza:95%
    Cor e Forma:Solid
    Peso molecular:265.23
  • Chrexanthomycin C


    <p>Chrexanthomycin C, orally active, binds DNA (G4C2)4 G4, Kd 2.8 mM, potential in ALS research.</p>
    Fórmula:C31H24O15
    Cor e Forma:Solid
    Peso molecular:636.51
  • Anti-EMMPRIN/CD147 Antibody


    Anti-EMMPRIN/CD147 Antibody is a human-derived antibody expressed in CHO cells, targeting Basigin. For an isotype control, refer to HumanIgG1kappa, Isotype Control.
    Cor e Forma:Odour Liquid
  • wrwyar-NH2 TFA


    <p>wrwyar-NH2 (TFA) serves as the control peptide for wrwycr-NH2.</p>
    Cor e Forma:Odour Solid
  • 5'-O-DMT-rU

    CAS:
    5’-O-DMT-rU is a modified nucleoside and can be used to synthesize RNA.
    Fórmula:C30H30N2O8
    Cor e Forma:Solid
    Peso molecular:546.57
  • Uridine triphosphate 13C9,15N2 sodium

    CAS:
    Uridine triphosphate 13C9,15N2 sodium is an isotopically labeled.UTP is a key in RNA synthesis molecule a substrate for RNA polymerase.
    Fórmula:C9H1415N2NaO15P3
    Cor e Forma:Solid
    Peso molecular:517.04
  • HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt

    CAS:
    HOE 33187-O-CONH-PEG4-phenol-thiophenone-NHPh-COOEt inhibits pre-miR-21 RNA, potential for cancer research.
    Fórmula:C57H62N8O10S
    Cor e Forma:Solid
    Peso molecular:1051.21
  • N4-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl)-5-methylcytidine


    <p>N4-Benzoyl-3'-O-DMT cytidine analog inhibits DNA methyltransferases like Zebularine.</p>
    Fórmula:C41H43N3O9
    Cor e Forma:Solid
    Peso molecular:721.79
  • Erythromycin thiocyanate

    CAS:
    Erythromycin thiocyanate, a macrolide from Streptomyces erythreus, binds 50S ribosomes, halting protein synthesis in bacteria.
    Fórmula:C38H68N2O13S
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:793.02
  • (1S,3R,5R)-PIM447 dihydrochloride


    (1S,3R,5R)-PIM447 (dihydrochloride) an inhibitor of PIM(IC50 of 0.095 μM for Pim1, 0.522 μM for Pim2 and 0.369 μM for Pim3).
    Fórmula:C24H25Cl2F3N4O
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:513.38
  • Guanosine triphosphate

    CAS:
    Guanosine triphosphate (GTP), a native nucleotide, and its derivatives may serve as specific inhibitors against COVID-19 [1].
    Fórmula:C10H16N5O14P3
    Cor e Forma:Solid
    Peso molecular:523.18
  • CCT241533 dihydrochloride

    CAS:
    Potent Chk2 inhibitor with 3 nM IC50, 63-fold more selective over Chk1, affects 84 kinases, reduces DNA damage response and apoptosis in cells.
    Fórmula:C23H29Cl2FN4O4
    Cor e Forma:Solid
    Peso molecular:515.41
  • CDK4/6-IN-23


    CDK4/6-IN-23 (Compound 42) is a potent and selective inhibitor of CDK4/6, displaying an IC50 of 11 nM for CDK6. This compound significantly activates immune cells and enhances IL-3 production. In mice undergoing 5-FU chemotherapy, CDK4/6-IN-23 demonstrates dual bone marrow protection and immunomodulatory effects.
    Fórmula:C32H34FN7O4
    Cor e Forma:Solid
    Peso molecular:599.655
  • Etrolizumab

    CAS:
    MEDI-578 is a CHO-expressed humanized monoclonal antibody targeting NGF/bNGF for the study of neurological and immune system disorders.
    Pureza:98.9% (SDS-PAGE); 96.6% (SEC-HPLC) - 98.9% (SDS-PAGE); 96.6% (SEC-HPLC)
    Cor e Forma:Liquid
  • DSPE-PEG2000-cRGD


    DSPE-PEG2000-cRGD is a PEG compound composed of DSPE and an αvβ3-targeting peptide (cRGD). The cRGD peptide specifically binds to αvβ3 on the surface of various cancer cells and neovascular cells. This compound can be utilized for drug delivery.
    Cor e Forma:Odour Solid
  • Nusinersen

    CAS:
    Nusinersen (nusinersen) is a antisense oligonucleotide (ASO) for the treatment of pediatric and adult spinal muscular atrophy (SMA) and increases SMN proteinss.
    Pureza:98.62%
    Cor e Forma:Solid
  • Chrysomycin A

    CAS:
    Chrysomycin A is an antibiotic that can be derived from Streptomyces.
    Fórmula:C28H28O9
    Cor e Forma:Solid
    Peso molecular:508.52
  • JH-XVI-178

    CAS:
    JH-XVI-178: potent CDK8/19 inhibitor with good pharmacokinetics, low clearance, moderate oral bioavailability.
    Fórmula:C22H22ClN7O
    Cor e Forma:Solid
    Peso molecular:435.92
  • JB300

    CAS:
    JB300 is a PROTAC-based compound that serves as a highly selective degrader of Aurora A, with a DC50 of 30 nM. It is utilized in cancer research. JB300 comprises the PROTAC target protein ligand MK-5108 [pink part], E3 ligase ligand Thalidomide-O-COOH [blue part], and PROTAC Linker Boc-NH-PEG2-C2-NH2 [black part]. The conjugate of the E3 ubiquitin ligase ligand and linker is Thalidomide-O-COOH-NH2-C2-PEG2-NH-Boc.
    Fórmula:C43H45ClFN7O10S
    Cor e Forma:Solid
    Peso molecular:906.375