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p53

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The p53 tumor suppressor is a 53 kDa nuclear phosphoprotein of 393 amino acids that is encoded by the TP53 gene (20 kb with 11 exons and 10 introns) and characterized by the presence of several structural and functional domains, including a N-terminus, a central core domain, a C-terminal region, a strongly basic carboxyl-terminal regulatory domain, a nuclear localization signal sequence and three nuclear export signal sequence. The p53 is considered as a major “guardian of genome” for its activities in a wide range of cellular events, including cell-cycle regulation, induction of apoptosis, gene amplification, DNA recombination, chromosomal segregation and cellular senescence.

Products Related to p53(152)

  • GC73604 structure
    GC73604MeOIstPyrd
    CAS: 2308548-54-9
    Purity: >99.00%

    MeOIstPyrd is an anti-skin cancer agent.

  • GC73719 structure
    GC73719BAY 1892005
    CAS: 2036352-13-1
    Purity: >99.00%

    BAY 1892005 is a regulator of p53 protein and acts on p53 condensates without causing mutant p53 reactivation.

  • GC73823 structure
    GC73823MMs02943764
    CAS: 708287-29-0
    Purity: >98.00%

    MMs02943764 is a 1,2,4-triazole derivative with anticancer activity.

  • GC73918 structure
    GC73918BAY 249716
    CAS: 696628-24-7
    Purity: >99.00%

    BAY 249716 stabilizes all three p53 protein variants.

  • GC73939 structure
    GC73939ATPase-IN-3
    CAS: 1134203-12-5
    Purity: >99.00%

    ATPase-IN-3 (compound 6) is a ATPase inhibitor.

  • GC74256 structure
    GC74256Condurango glycoside A
    CAS: 11051-90-4
    Purity: >95.00%

    Condurango glycoside A is an activator of p53.

  • GC74358 structure
    GC74358PNC-27 acetate
    Purity: >99.00%

    PNC-27 acetate, a chimeric p53-penetratin peptide binds to HDM-2 in a p53 peptide-like structure, induces selective membrane-pore formation and leads to cancer cell lysis.

  • GC78809 structure
    GC78809UCI-14
    CAS: 301312-49-2
    Purity: >98.00%

    UCI-14 is a gltA1/lprQ modulator with in vitro anti-tuberculosis activity against drug-sensitive and multidrug-resistant mycobacteria.

  • GC78961 structure
    GC78961GPS167
    CAS: 3034312-19-8
    Purity: >98.00%

    GPS167 is a CLK kinase inhibitor that potently and selectively inhibits recombinant human CLK1, CLK2 and CLK4.

  • GC78970 structure
    GC78970UCI-LC0019
    CAS: 1372406-51-3
    Purity: >98.50%

    UCI-LC0019 is a mutant p53 reactivator.

  • GC78971 structure
    GC78971UCI-1014
    CAS: 304896-41-1
    Purity: >98.00%

    UCI-1014 is a mutant p53 ( p53 R175H ) corrector/reactivator.

  • GC78972 structure
    GC78972MI-773 TFA
    CAS: 1303609-37-1
    Purity: >98.50%

    MI-773 TFA is an orally active, selective MDM2-p53 interaction inhibitor with a K i of 0.88 nM for MDM2.

  • GC78973 structure
    GC78973Peptide 234CM TFA
    Purity: >98.00%

    Peptide 234CM TFA is a peptide containing isoleucine at position 3, corresponding to the sequence of a point mutation in p53 codon 234.

  • GC78974 structure
    GC78974p53 (17-26) acetate
    Purity: >98.00%

    p53 (17-26) acetate is a peptide derived from the P53 MDM2 binding domain, with a K d of 50 nM for MDM2.

  • GC78980 structure
    GC78980Rhodojaponin VI
    CAS: 37720-87-9
    Purity: >99.50%

    Rhodojaponin VI is an orally active diterpenoid compound found in hododendron molle G.

  • GC79004 structure
    GC79004PMV6-PEG4-BI2536
    Purity: >98.00%

    PMV6-PEG4-BI2536 is an RIPTAC-like bifunctional molecule that promotes the formation of the p53 Y 220C -PLK1 ternary complex ( EC 50 = 1.4 μM).

  • GC79049 structure
    GC79049CG-1521
    CAS: 674767-29-4
    Purity: >95.50%

    CG-1521 is a histone deacetylase ( HDAC ) inhibitor that stabilizes Ac-Lys373 P53, increases P21 levels and HDAC2 degradation.

  • GC79111 structure
    GC79111CK2-TN03
    CAS: 313226-24-3
    Purity: >98.00%

    CK2-TN03 is an ATP-competitive casein kinase 2 ( CK2 ) inhibitor, with an IC 50 of 165 nM and a K i of 20 nM.

  • GC79144 structure
    GC79144MC3817 free base
    Purity: >98.00%

    MC3817 free base is a selective DNMT1 inhibitor.

  • GC79145 structure
    GC79145MC3817
    Purity: >99.50%

    MC3817 is a selective DNMT1 inhibitor.

  • GC79146 structure
    GC79146Ischemin
    CAS: 1357059-00-7
    Purity: >99.50%

    Ischemin is a CBP bromodomain inhibitor that inhibits p53 interaction with CBP and transcriptional activity in cells.

  • GC79976 structure
    GC79976Chitosan oligosaccharide (MW 2000)
    Purity: >98.00%

    Chitosan oligosaccharide (MW 2000) is a natural oligomer derived from chitosan, with a molecular weight of 2000 Da.

  • GC80853 structure
    GC80853(4R,5S)-YX-02-030
    CAS: 3049077-01-9
    Purity: >99.50%

    (4R,5S)-YX-02-030 is an isomer of YX-02-030.

  • GC80881 structure
    GC80881PROTAC DAPK1 Degrader-1
    CAS: 3063030-38-3
    Purity: >96.50%

    PROTAC DAPK1 Degrader-1 is a death-associated protein kinase 1 (DAPK1) degrader with a DC 50 of 119.6 nM.