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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.

Subcategorias de "Ciclo celular/Ponto de verificação"

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Foram encontrados 3935 produtos de "Ciclo celular/Ponto de verificação"

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  • Ganodermaones B


    Ganodermaones B is a renal fibrosis inhibitor. Ganodermaones B inhibits TGF-β1-induced collagen I and fibronectin expression .
    Fórmula:C21H26O5
    Cor e Forma:Solid
    Peso molecular:358.43

    Ref: TM-T72798

    25mg
    1.369,00€
    50mg
    1.783,00€
    100mg
    2.250,00€
  • 3'-β-C-ethynyl-N6-(m-trifluoromethyl benzyl)adenosine


    3’-Beta-C-ethynyl-N6-(m-trifluoromethyl benzyl)adenosine is an adenosine analog.
    Fórmula:C20H18F3N5O4
    Cor e Forma:Solid
    Peso molecular:449.38

    Ref: TM-T75048

    5mg
    A consultar
    50mg
    A consultar
  • 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

    Ref: TM-T74244

    5mg
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    50mg
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  • PROTAC MTP3 degrade-1


    PROTACMTP3 degrade-1 is a PROTAC degrader for MYC.
    Fórmula:C44H38N6O8
    Cor e Forma:Solid
    Peso molecular:778.27511

    Ref: TM-T207468

    10mg
    A consultar
    50mg
    A consultar
  • L-5-Methyluridine

    CAS:
    L-5-Methyluridine, an L-configuration of 5-Methyluridine, is an endogenous methylated nucleoside present in human fluids.
    Fórmula:C10H14N2O6
    Cor e Forma:Solid
    Peso molecular:258.23

    Ref: TM-T74653

    5mg
    A consultar
    50mg
    A consultar
  • S-MGB-234

    CAS:
    S-MGB-234 treats AAT, effective against T. congolense and T. vivax, no cross-resistance or shared transport with diamidines.
    Fórmula:C30H32N8O4
    Cor e Forma:Solid
    Peso molecular:568.638

    Ref: TM-T39397

    25mg
    1.369,00€
  • RA-V


    RA-V is a natural product that can be used as a reference standard.
    Fórmula:C160H202N24O41
    Cor e Forma:Solid
    Peso molecular:3117.5

    Ref: TM-T124482

    1mg
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    5mg
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  • S3 Fragment


    S3 Fragment is a biologically active peptide featuring the amino-terminal phosphorylation site unique to Xenopus ADF/cofilin, which is the target of LIM kinase
    Fórmula:C73H120N18O24S2
    Cor e Forma:Solid
    Peso molecular:1697.97

    Ref: TM-T80253

    5mg
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    50mg
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  • Cyclic tri-AMP

    CAS:
    Cyclic tri-AMP is a key element of the cyclic oligonucleotide-based anti-phage signaling system (CBASS), functioning as a second messenger in the immune defense against viral infections. It activates DNA endonuclease NucC through binding, leading to cell death and demonstrating antiviral properties.
    Fórmula:C30H36N15O18P3
    Cor e Forma:Solid
    Peso molecular:987.62

    Ref: TM-T88085

    10mg
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    50mg
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  • xStAx-VHLL


    Selective β-catenin degrader, xStAx-VHL peptide, lowers its levels in cells and inhibits tumor growth.
    Cor e Forma:Liquid

    Ref: TM-T36275

    100µg
    1.783,00€
  • WRN inhibitor 17

    CAS:
    WRN inhibitor 17 (Compound 250) is an orally active inhibitor of Werner syndrome ATP-dependent helicase (WRN), specifically targeting the helicase domain activity of WRN. It holds potential for use in cancer research.
    Fórmula:C33H34F4N4O6S
    Cor e Forma:Solid
    Peso molecular:690.71

    Ref: TM-T203305

    10mg
    A consultar
    50mg
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  • Carboxy pyridostatin trifluoroacetate salt


    Carboxy pyridostatin trifluoroacetate salt exhibits higher molecular specificity for RNA over DNA G4s.
    Fórmula:C37H35F3N10O9
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:820.73

    Ref: TM-T13595

    100mg
    A consultar
    500mg
    A consultar
  • Ac-MRGDH-NH2


    Ac-MRGDH-NH2 is a pentapeptide containing the RGD sequence. It is utilized in the synthesis of the diastereomeric prodrugs Λ- and Δ-[Ru(Ph2phen)2(κS,κN-(Ac-MRGDH-NH2))]Cl2. In these prodrugs, Ac-MRGDH-NH2 serves as a photolabile protecting group for the cytotoxic diruthenium aqua complexes [Ru(Ph2phen)2(OH2)2]2+, offering integrin targeting and photoactivation properties. Consequently, Ac-MRGDH-NH2 can be applied in studies exploring tumor-targeted photoactivatable chemotherapy.
    Fórmula:C25H41N11O8S
    Cor e Forma:Solid
    Peso molecular:655.727

    Ref: TM-TP3057

    10mg
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    50mg
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  • Lys-Gln-Ala-Gly-Asp-Val

    CAS:
    KQAGDV is a fibrinogen γ-chain cell adhesion peptide, targeting α2bβ3 integrin, and binds SMCs.
    Fórmula:C25H44N8O10
    Cor e Forma:Solid
    Peso molecular:616.66

    Ref: TM-T76376

    5mg
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    50mg
    A consultar
  • Pseudouridimycin

    CAS:
    Pseudouridimycin: a C-nucleoside antibiotic, inhibits bacterial RNAP, targets Gram-negative and Gram-positive bacteria.
    Fórmula:C17H26N8O9
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:486.44

    Ref: TM-T16673

    10mg
    762,00€
  • 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

    Ref: TM-T36299

    100mg
    47,00€
  • Clofarabine-5'-triphosphate

    CAS:
    Clofarabine-5'-triphosphate is a metabolite of Clofarabine, produced via phosphorylation by deoxycytidine kinase (dCK). It exhibits cytotoxicity in cancer cells by inhibiting DNA synthesis and DNA repair.
    Fórmula:C10H14ClFN5O12P3
    Cor e Forma:Solid
    Peso molecular:543.62

    Ref: TM-T203136

    10mg
    A consultar
    50mg
    A consultar
  • PROTAC CDK9 degrader-2

    CAS:
    PROTAC CDK9 degrader-2, potent, selective, IC50 17 μM in MCF-7, wogonin-derived, targets CRBN.
    Fórmula:C39H36N6O10
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:748.74

    Ref: TM-T17728

    100mg
    A consultar
    500mg
    A consultar
  • HEMTAC WEE1 degrader-1

    CAS:
    HEMTACWEE1degrader-1 is a WEE1-targeting heterobifunctional chimeric degrader (HEMTAC) facilitated by HSP90, exhibiting an HSP90 enzyme inhibitory activity with an IC50 of 16.76 nM. It enhances the ubiquitination and subsequent degradation of WEE1, effectively blocking the G2/M cell cycle transition. This compound shows anticancer properties in patient-derived xenograft (PDX) models of acute myeloid leukemia (AML). HEMTACWEE1degrader-1 is utilized in AML research.
    Fórmula:C57H71N15O6
    Cor e Forma:Solid
    Peso molecular:1062.27

    Ref: TM-T207012

    10mg
    A consultar
    50mg
    A consultar
  • 5'-O-DMT-N4-Bz-2'-F-dC

    CAS:
    5’-O-DMT-N4-Bz-2’-F-dC is a nucleoside with protective and modification effects.
    Fórmula:C37H34FN3O7
    Cor e Forma:Solid
    Peso molecular:651.68

    Ref: TM-T37137

    100mg
    47,00€
    1mL*10mM (DMSO)
    52,00€