Pifithrin-α, p-Nitro, Cyclic NEW
| Price | $34 | $48 | $80 |
| Package | 1mg | 2mg | 5mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2025-10-31 |
Product Details
| Product Name: Pifithrin-α, p-Nitro, Cyclic | CAS No.: 60477-38-5 |
| Purity: 99.97% | Supply Ability: 10g |
| Release date: 2025/10/31 |
Product Introduction
Bioactivity
| Name | Pifithrin-α, p-Nitro, Cyclic |
| Description | Pifithrin-α, p-Nitro, Cyclic (PFN-α) is a cell-permeable, active-form inhibitor of p53. |
| In vitro | Pifithrin-α, p-Nitro, Cyclic (PFN-α) significantly inhibits p53-induced cell death and p21/WAF1 expression in cortical neurons exposed to etoposide, requiring concentrations an order of magnitude lower than PFT-α[1]. |
| In vivo | Intraocular administration of pifithrin-α at a concentration of 6 µM modestly enhances the survival of retinal ganglion cells (RGC), while it remains ineffective at 0.06 µM. Despite the observed in vitro benefits, pifithrin-α, p-Nitro, Cyclic (PFN-α) demonstrates no in vivo efficacy, even at the 6 µM concentration. Furthermore, pifithrin-α, p-Nitro, Cyclic exhibits a half-life (t1/2) of 6 hours under biological conditions[1]. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO : 5 mg/mL (16.70 mM), Sonication is recommended. DMF : 12.5 mg/mL (41.76 mM), Sonication is recommended. |
| Keywords | WAF1 | posttranscriptional | Pifithrin-α, p-Nitro, Cyclic | Pifithrinα, pNitro, Cyclic | Pifithrin-alpha, p-Nitro, Cyclic | Pifithrin-a, p-Nitro, Cyclic | Pifithrin α, p Nitro, Cyclic | PFN-alpha | PFN-a | p53-triggered | P53 | p21 | neurons | MDM-2/p53 | Inhibitor | inhibit | expression | death | cortical | cell |
| Inhibitors Related | 10-Hydroxydecanoic Acid | Flubendazole | PRIMA-1 | Rotenone | XI-006 | 2,5-Dihydroxybiphenyl | Thiabendazole | Minocycline hydrochloride | Triglycidyl isocyanurate | C16 Ceramide | Indole-3-carbinol | Diethanolamine hydrochloride |
| Related Compound Libraries | Ferroptosis Compound Library | Glycometabolism Compound Library | Bioactive Compound Library | Ubiquitination Compound Library | Anti-Cancer Metabolism Compound Library | Pyroptosis Compound Library | Inhibitor Library | Metabolism Compound Library | PPI Inhibitor Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | Transcription Factor-Targeted Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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United States- Since: 2011-01-07
- Address: 36 Washington Street, Wellesley Hill, MA
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