uitsluitend voor onderzoeksdoeleinden
Cat.Nr.: S7724
Chemische structuur
| Gerelateerde doelwitten | Bcl-2 Caspase PD-1/PD-L1 Ferroptosis Apoptosis related Synthetic Lethality STAT TNF-alpha Ras KRas |
|---|---|
| Overige p53 Inhibitoren | CBL0137 Hydrochloride Pifithrin-α (PFTα) Hhydrobromide Pifithrin-μ RITA Serdemetan (JNJ-26854165) NSC 319726 (ZMC1) PRIMA-1 Tenovin-1 NSC59984 NSC348884 |
| Cellijnen | Assaytype | Concentratie | Incubatietijd | Formulering | Activiteitsbeschrijving | PMID |
|---|---|---|---|---|---|---|
| NALM-6 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| UoCB-6 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| EU-3 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| MUTZ-5 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| KOPN-8 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| RS4;11 | Cell viability assay | high sensitivity and cell death induction in all TP53mut leukemias, but low APR-246 sensitivity in TP53wt ALL | 31073076 | |||
| SKBR3 | Cell cycle assay | 5 µM | 2 weeks | lapatinib in combination with APR-246 caused a lower level of G1 arrest and an increase in the sub-G1 fraction | 30743996 | |
| BT549 | Cell viability assay | IC50=3.1 μM | 30196236 | |||
| MDA-MB-468 | Cell viability assay | IC50=5 μM | 30196236 | |||
| MDA-MB-231 | Cell viability assay | IC50=4.1 μM | 30196236 | |||
| HCC1143 | Cell viability assay | IC50=6.8 μM | 30196236 | |||
| MDA-MB-453 | Cell viability assay | IC50=0.9 μM | 30196236 | |||
| SKBR3 | Cell viability assay | IC50=5.1 μM | 30196236 | |||
| UACC812 | Cell viability assay | IC50=11.3 μM | 30196236 | |||
| MCF7 | Cell viability assay | IC50=31.1 μM | 30196236 | |||
| MCF10A | Cell viability assay | IC50=5.2 μM | 30196236 | |||
| UMSCC10A | Cell viability assay | 0-50 μM | 72 h | suppressed cell survival and bore a modest effect on the killing of HNSCC cells | 29348462 | |
| FaDu | Cell viability assay | 0-50 μM | 72 h | suppressed cell survival and bore a modest effect on the killing of HNSCC cells | 29348462 | |
| TC32 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells | 29435139 | |||
| DAOY | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells | 29435139 | |||
| SJ-GBM2 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells | 29435139 | |||
| A673 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells | 29435139 | |||
| SK-N-MC | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells | 29435139 | |||
| BT-37 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells | 29435139 | |||
| NB-EBc1 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells | 29435139 | |||
| Saos-2 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells | 29435139 | |||
| SK-N-SH | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells | 29435139 | |||
| NB1643 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells | 29435139 | |||
| LAN-5 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells | 29435139 | |||
| BT-12 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells | 29435139 | |||
| OHS-50 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells | 29435139 | |||
| MG 63 (6-TG R) | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells | 29435139 | |||
| Rh41 | qHTS assay | qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells | 29435139 | |||
| Klik om meer experimentele gegevens over de cellijn te bekijken | ||||||
| Moleculair gewicht | 199.25 | Formule | C10H17NO3 |
Opslag (Vanaf de ontvangstdatum) | |
|---|---|---|---|---|---|
| CAS-nr. | 5291-32-7 | SDF downloaden | Opslag van stamoplossingen |
|
|
| Synoniemen | PRIMA-1MET | Smiles | COCC1(C(=O)C2CCN1CC2)CO | ||
|
In vitro |
DMSO
: 40 mg/mL
(200.75 mM)
Water : 40 mg/mL Ethanol : 40 mg/mL |
|
In vivo |
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Stap 1: Voer de onderstaande informatie in (Aanbevolen: Een extra dier voor het geval van verlies tijdens het experiment)
Stap 2: Voer de in vivo formulering in (Dit is alleen de calculator, geen formulering. Neem eerst contact met ons op als er geen in vivo formulering is in het gedeelte Oplosbaarheid.)
Berekeningsresultaten:
Werkconcentratie: mg/ml;
Methode voor het bereiden van DMSO-mastervloeistof: mg geneesmiddel vooraf opgelost in μL DMSO ( Concentratie mastervloeistof mg/mL, Neem eerst contact met ons op als de concentratie de DMSO-oplosbaarheid van de partij geneesmiddel overschrijdt. )
Methode voor het bereiden van in vivo formulering: Neem μL DMSO mastervloeistof, voeg vervolgens toeμL PEG300, mengen en helder maken, voeg vervolgens toeμL Tween 80, mengen en helder maken, voeg vervolgens toe μL ddH2O, mengen en helder maken.
Methode voor het bereiden van in vivo formulering: Neem μL DMSO mastervloeistof, voeg vervolgens toe μL Maïsolie, mengen en helder maken.
Opmerking: 1. Zorg ervoor dat de vloeistof helder is voordat u het volgende oplosmiddel toevoegt.
2. Zorg ervoor dat u het/de oplosmiddel(en) in de juiste volgorde toevoegt. U moet ervoor zorgen dat de verkregen oplossing, bij de vorige toevoeging, een heldere oplossing is voordat u verdergaat met het toevoegen van het volgende oplosmiddel. Fysische methoden zoals vortexen, echografie of een warmwaterbad kunnen worden gebruikt om het oplossen te bevorderen.
| Targets/IC50/Ki |
Mutant p53
|
|---|---|
| In vitro |
Eprenetapopt (APR-246), also known as PRIMA-1MET, is the first clinical-stage compound that reactivates mutant p53 and induces apoptosis. It is a prodrug that is converted to the active compound methylene quinuclidinone (MQ), a Michael acceptor that binds to cysteine residues in mutant p53 and restores its wild-type conformation. This compound not only reactivates p53 but also decreases intracellular glutathione levels in a dose-dependent manner. It can trigger apoptosis in a p53-independent manner by inducing ROS and endoplasmic reticulum (ER) stress and by inhibiting thioredoxin reductase 1 (TrxR1). It was also reported that APR-246 induces cell death in myeloma cells independently of p53 status by impairing the GSH/ROS balance. PRIMA-1Met/APR-246 efficiently inhibited the growth of the SCLC cell lines expressing mutant p53 in vitro and induced apoptosis, associated with increased fraction of cells with fragmented DNA, caspase-3 activation, PARP cleavage, Bax and Noxa upregulation and Bcl-2 downregulation in the cells. |
| In vivo |
In a Phase I/II clinical dose-finding study on hematological malignancies and prostate cancer, Eprenetapopt (APR-246) showed a good safety profile, and both clinical and p53-dependent biological responses were observed. It is well tolerated in animal studies, and single treatment with this compound inhibits tumor growth by 21% in mice bearing the aggressively growing A2780-CP20 tumor xenografts. |
Referenties |
|
| Methoden | Biomarkers | Afbeeldingen | PMID |
|---|---|---|---|
| Western blot | FL-PARP / Cleaved PARP p-p53 |
|
26452133 |
| Growth inhibition assay | Cell viability |
|
26452133 |
(gegevens van https://clinicaltrials.gov, bijgewerkt op 2022-03-10)
| NCT-nummer | Rekrutering | Aandoeningen | Sponsor/Medewerkers | Startdatum | Fasen |
|---|---|---|---|---|---|
| NCT04990778 | WITHDRAWN | Recurrent Mantle Cell Lymphoma; Refractory Mantle Cell Lymphoma |
M.D. Anderson Cancer Center |
2021-11-30 | PHASE2 |
| NCT04383938 | COMPLETED | Bladder Cancer; Gastric Cancer; Non Small Cell Lung Cancer; NSCLC; Urothelial Carcinoma; Advanced Solid Tumor |
Aprea Therapeutics |
2020-06-25 | PHASE1; PHASE2 |
| NCT04214860 | COMPLETED | Myeloid Malignancy |
Aprea Therapeutics |
2019-12-13 | PHASE1 |
| NCT03931291 | COMPLETED | Acute Myeloid Leukemia or Myelodysplastic Syndromes |
Aprea Therapeutics |
2019-09-16 | PHASE2 |
| NCT04419389 | TERMINATED | Non Hodgkin Lymphoma; Chronic Lymphocytic Leukemia; Mantle Cell Lymphoma |
Aprea Therapeutics |
2021-03-02 | PHASE1; PHASE2 |
| NCT03745716 | COMPLETED | MDS |
Aprea Therapeutics |
2019-01-11 | PHASE3 |