(Translated by https://www.hiragana.jp/)
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p53

Tumor protein p53, also known as p53, cellular tumor antigen p53 (UniProt name), the Guardian of the Genome, phosphoprotein p53, tumor suppressor p53, antigen NY-CO-13, or transformation-related protein 53 (TRP53), is any isoform of a protein encoded by homologous genes in various organisms, such as TP53 (humans) and Trp53 (mice). This homolog (originally thought to be, and often spoken of as, a single protein) is crucial in multicellular organisms, where it prevents cancer formation, and thus functions as a tumor suppressor. As such, p53 has been described as "the guardian of the genome" because of its role in conserving stability by preventing genome mutation.

  • CBL0137 hydrochloride
    T43611197397-89-9
    CBL0137 hydrochloride (Curaxin-137 hydrochloride) activates p53 and inhibits NF-kB (EC50: 0.37 0.47 μみゅーM) in the cell-based p53 and NF-kB reporter assays, respectively. It also suppresses histone chaperone FACT.
    • ¥10,000
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  • Indole-3-carbinol
    T2947700-06-1
    Indole-3-carbinol (I3C), a naturally occurring, orally available cleavage product of the glucosinolate glucobrassicanin, inhibits NF-κかっぱB and IκかっぱBαあるふぁ kinase activation.
    • ¥7,000
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  • Magnolol
    T3000528-43-8
    Magnolol (5,5'-Diallyl-2,2'-biphenyldiol) is a dual agonist of RXRαあるふぁ( EC50=10.4 μみゅーM) and PPARγがんま(EC50=17.7 μみゅーM). It blocks TNF-αあるふぁ-induced NF-KB activation.
    • ¥9,000
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  • 1-[2,4-Dihydroxy-6-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one
    TN5263569-83-5
    1-[2,4-Dihydroxy-6-methoxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one (Xanthohumol) , prenylchacone flavonoid, is a natural product with multi-biofunctions purified from Hops Humulus lupulus,is effective against HIV-1 and might serve as an interesting lead compound. It may represent a novel chemotherapeutic agent for HIV-1 infection.
    • ¥8,500
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  • p53-Mdm2 inhibitor 4
    T67698350678-63-6
    p53-Mdm2 inhibitor 4 inhibits the p53-MDM2 protein-protein interaction.
    • ¥11,500
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  • CT-1
    T270931983924-33-9在庫ざいこ
    CT-1 is a DNA minor groove ligand and causes p53-dependent breast cancer cell apoptosis.
    • ¥27,000
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  • ReACp53 acetate
    TP1427L
    ReACp53 acetate could inhibit p53 amyloid formation and rescue p53 function in cancer cell lines.
    • ¥21,000
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  • RO-5963
    T167711416663-77-8在庫ざいこ
    RO-5963 is a dual inhibitor of p53-MDM2 and p53-MDMX (IC50s: ~17 nM and ~24 nM, respectively).
    • ¥24,500
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  • DPBQ
    T110927029-89-2在庫ざいこ
    • ¥24,500
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  • Roslin 2 bromide
    T2473029574-21-8在庫ざいこ
    Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5, exhibiting anticancer effects.
    • ¥10,000
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  • P53R3
    T41068922150-12-7在庫ざいこ
    P53R3 is a potent reactivator of p53, effectively restoring sequence-specific DNA binding to several p53 hot spot mutants, namely p53 R175H, p53 R248W, and p53 R273H. This compound exhibits p53-dependent antiproliferative effects with significantly higher specificity compared to PRIMA-1 and promotes the recruitment of both wild-type p53 and p53 M237I to various target gene promoters. Additionally, P53R3 markedly increases the mRNA, total protein, and cell surface expression of death receptor 5 (DR5), demonstrating its utility in cancer research.
    • ¥16,000
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  • Pifithrin-αあるふぁ, p-Nitro, Cyclic
    T1247260477-38-5
    Pifithrin-αあるふぁ, p-Nitro, Cyclic (PFN-αあるふぁ) is a cell-permeable, active-form inhibitor of p53.
    • ¥8,000
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  • RITA
    T1798213261-59-7
    RITA (NSC-652287)(NSC-652287) induced cross-links of both DNA-DNA and DNA-protein with no detectable DNA single-strand breaks. RITA, like nutlin-3, can disrupt the p53/Mdm2 interaction.
    • ¥7,000
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  • Pifithrin-βべーた hydrobromide
    T3637511296-88-1
    Pifithrin-βべーた hydrobromide (Cyclic PFT-αあるふぁ) is an inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and apoptosis. Protects against neuronal death in models of stroke and neurodegenerative disorders. Active in vivo; protects mice from the side-effects of Y therapy associated with p53 induction. Supresses self-renewal of embryonic stem cells. Also aryl hydrocarbon receptor (AHR) agonist, causes upregulation of AHR target gene CYP1A1 (EC50 = 1.1 μみゅーM).
    • ¥8,000
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  • Serdemetan
    T2243881202-45-5
    Serdemetan (JNJ-26854165) is an orally bioavailable HDM2 antagonist with potential antineoplastic activity.
    • ¥9,000
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  • Kevetrin hydrochloride
    T318466592-89-0
    Kevetrin hydrochloride (4-Isothioureidobutyronitrile hydrochloride) is a small molecule and activator of the tumor suppressor protein p53, with potential antineoplastic activity.
    • ¥9,000
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  • NSC348884
    T690981624-55-7
    NSC348884 is a nucleophosmin inhibitor disrupts oligomer formation and induces apoptosis, inhibits cell proliferation at an IC50 of 1.7-4.0 μみゅーM in distinct cancer cell lines.
    • ¥8,000
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  • Rotenone
    T297083-79-4
    Rotenone (Rotocide) is a natural product and a botanical insecticide. Rotenone is a mitochondrial electron transport complex I inhibitor that promotes the production of reactive oxygen species in mitochondria and induces apoptosis.
    • ¥10,000
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  • Verbascoside
    T337561276-17-3
    Verbascoside (Kusaginin) is a protein kinase C inhibitor with antimicrobial, anti-inflammatory activities.
    • ¥13,500
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  • Pifithrin-αあるふぁ hydrobromide
    T270763208-82-2
    Pifithrin-αあるふぁ hydrobromide (Pifithrin-αあるふぁ hydrobromide) is a p53 inhibitor, inhibiting p53-dependent transactivation of p53-responsive genes.
    • ¥7,500
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  • Brigimadlin
    T699232095116-40-6
    Brigimadlin (BI 907828) is an orally active and highly potent E3 ubiquitin-protein ligase MDM2-p53 antagonist with antitumor activity.Brigimadlin can be used to study metastatic BTC, PDAC, lung adenocarcinoma, or bladder cancer.
    • ¥62,000
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  • Eprenetapopt
    T44145291-32-7
    Eprenetapopt (PRIMA-1Met) restores wild-type conformation and function to mutant p53, and triggers apoptosis in tumor cells. PRIMA-1MET also targets the selenoprotein thioredoxin reductase 1 (TrxR1), a key regulator of cellular redox balance.
    • ¥15,500
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  • Tenovin-6 Hydrochloride
    T84801011301-29-3
    Tenovin-6 Hydrochloride is an SIRT1, SIRT2 and HDAC8 inhibitor(IC50s of 21 μみゅーM, 10 μみゅーM, and 67 μみゅーM for SirT1, SirT2, and SirT3, respectively), and is also a potent p53 activator .
    • ¥7,500
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  • NSC59984
    T6910803647-40-7
    NSC59984, a p53 pathway activator, induces mutant p53 protein degradation and p73 activation.
    • ¥15,000
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  • PK11007
    T7703874146-69-7
    PK11007 is an anti-p53 drug.
    • ¥7,500
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  • Phenoxodiol
    T1652281267-65-4
    Phenoxodiol (Idronoxil) activates the mitochondrial caspase system, inhibits X-linked inhibitor of apoptosis(XIAP), disrupts FLICE inhibitory protein(FLIP) expression, and sensitizes the cancer cells to Fas-mediated apoptosis. Phenoxodiol induces cell cycle arrest in the G1 S phase of the cell cycle and upregulates p21WAF1 via a p53 independent manner. Phenoxodiol also inhibits DNA topoisomerase II.
    • ¥14,000
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  • CP-31398 dihydrochloride
    T216481217195-61-3
    CP-31398 dihydrochloride is a p53 stabilizer which stabilizes the active conformation of p53 and promotes p53 activity in cancer cell lines with mutant or wild-type p53.
    • ¥7,500
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  • ZMC1
    T246471555-25-4
    NSC-319726 (ZMC1), a mutant p53R175 reactivator, suppresses growth of fibroblasts that expresses the p53R175 mutation (IC50 = 8 nM).
    • ¥7,500
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  • HBX 41108
    T21527924296-39-9
    HBX 41108 (HBX-41108) is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBX 41108 inhibited deubiquitination of p53 mediated by USP7 in a dose-dependent manner with an IC50 of 0.8μみゅーM.
    • ¥11,000
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  • Benzonitrile, 3,3'-[(2-oxo-1,3-cyclohexanediylidene)dimethylidyne]bis-
    T912963476-70-0
    Benzonitrile, 3,3'-[(2-oxo-1,3-cyclohexanediylidene)dimethylidyne]bis- is an inhibitor of p53 with an IC50 value of 0.35 μみゅーM
    • ¥17,000
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  • MIRA-1
    T2298072835-26-8
    MIRA-1 (WRN Helicase Inhibitor) is a restorer of wild-type p53 conformation/cellular function and selectively inhibits Werner syndrome WRN helicase activity with an IC50 of 20 µM.
    • ¥8,000
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  • UC2288
    T96981394011-91-6
    UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.
    • ¥9,500
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  • XI-006
    T661058131-57-0
    XI-006 (XI-006) suppresses MDMX with IC50 of 2.5 μみゅーM, leading to enhanced p53 stabilization activation and DNA damage, and also regulates MDM2, an E3 ligase.
    • ¥12,000
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  • Amifostine thiol dihydrochloride
    TQ013314653-77-1
    Amifostine thiol dihydrochloride (WR 1065) can activate p53 through a JNK-dependent signaling pathway. It also protects normal tissues from the toxic effects of certain cancer drugs.
    • ¥11,000
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  • RO8994
    T35171309684-94-3
    RO8994 is a highly effective and specific inhibitor of spiroindolinone small-molecule MDM2, with IC50 of 20 nM (MTT proliferation assays) and 5 nM (HTRF binding assays).
    • ¥8,000
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  • Tenovin-1
    T1919380315-80-0
    Tenovin-1 inhibits protein-deacetylating activities of SirT1 and SirT2 and protects against MDM2-mediated p53 degradation, which involves ubiquitination.
    • ¥11,500
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  • Moringin
    TN458373255-40-0
    Moringin is an isothiocyanate obtained from myrosinase-mediated hydrolysis of the glucosinolate precursor glucoMoringin present in Moringa oleifera seeds. Moringin has anti-inflammatory and antioxidative properties.
    • ¥32,000
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  • COTI-2
    T43251039455-84-9
    COTI-2, an orally available thiosemicarbazone, is an activator of mutant forms of the p53 protein with potential antineoplastic activity.
    • ¥9,500
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  • Ergosta-4,6,8(14),22-tetraen-3-one
    TN161719254-69-4
    Ergosta-4,6,8(14),22-tetraen-3-one exhibits cytotoxic activity against human gastric cancer cells and can induce G2 M cell cycle arrest and apoptosis in human hepatocellular carcinoma (HepG2) cells. These findings could facilitate the further use of various medicinal fungi in cancer treatment.
    • ¥73,000
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  • Cristacarpin
    TN371974515-47-2
    Cristacarpin exhibits moderate but selective activity towards DNA repair-deficient yeast mutants. It promotes endoplasmic reticulum (ER) stress, leading to sub-lethal reactive oxygen species (ROS) generation and which eventually terminates by triggering s
    • ¥454,500
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  • SCH529074
    T37042922150-11-6
    SCH529074 is a selective activator of p53 (Ki = 1 μみゅーM) and can be used in studies about non-small-cell lung carcinoma. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53.
    • ¥7,000
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  • Pseudoginsenoside Rh2
    TN21141370264-16-6
    Pseudoginsenoside Rh2 has cytotoxicity, it induces mitochondrial apoptosis in A549 cells and is responsible for excessive activation of the Ras/Raf/ERK/p53 pathway. (20Z) -Pseudoginsenoside Rh2 and (20E)-Pseudoginsenoside Rh2 have antioxidative activity.
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  • BAY 1892005
    T777682036352-13-1
    BAY 1892005 is a p53 protein modulator that targets the p53 condenser for the study of diseases associated with misfolded p53 protein
    • ¥21,500
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  • Pinoresinol
    TN2080487-36-5
    Pinoresinol ((+)-Pinoresinol) has antiinflammatory, hepatoprotective, and fungicidal activities, it can protect pial microcirculation from I-reperfusion injury, to increase nitric oxide release and to reduce oxidative stress preserving pial blood flow distribution; it may exert pharmacologically interesting effects via modulation of the insulin-like signalling pathway in C.elegans. Pinoresinol causes an upregulation of the CDK inhibitor p21(WAF1 Cip1) both at mRNA and protein levels, inhibits NF-kappaB and activating protein 1 (AP-1).
    • ¥12,000
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  • 7alpha,15-Dihydroxydehydroabietic acid
    TN3252155205-64-4
    7alpha,15-Dihydroxydehydroabietic acid may exhibit significant cytotoxic activity.
    • ¥472,500
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  • p53-MDM2-IN-1
    T72026381717-91-5
    p53-MDM2-IN-1 (Example 30), an inhibitor of the p53-MDM2 X protein interaction, exhibits a K i value of 23.35 µM and holds potential for applications in anti-tumor research.
    • ¥45,000
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  • (-)-Curine
    TN1156436-05-5
    (-)-Curine can inhibit viability of hepatocellular carcinoma cells in regardless of p53 status.
    • ¥44,000
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  • Uncarinic acid E
    TN5201277751-61-8
    Uncarinic acid E has anti-cancer activity, it induces apoptosis in HepG2 cells via accumulation of p53, alters the Bax/Bcl-2 ratio, and activates caspases, resulting in cytochrome c release from the mitochondria. A mixture of uncarinic acid E and 27-O-p-(
    • ¥135,500
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  • Liriodenine
    TN1875475-75-2
    Liriodenine is a potent inhibitor of topoisomerase II (EC 5.99.1.3) both in vivo and in vitro, it has antitumor, antibacterial and antifungal activities, it can suppress ventricular arrhythmias induced by myocardial ischaemia reperfusion, through inhibiti
    • ¥124,000
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  • Imbricatolic acid
    TN42506832-60-6
    Imbricatolic acid can prevent cell cycle progression in p53-null CaLu-6 cells.
    • ¥142,500
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