PFI-1 NEW
| Price | $70 | $123 | $198 |
| Package | 10mg | 25mg | 50mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2025-09-28 |
Product Details
| Product Name: PFI-1 | CAS No.: 1403764-72-6 |
| Purity: 99.19% | Supply Ability: 10g |
| Release date: 2025/09/28 |
Product Introduction
Bioactivity
| Name | PFI-1 |
| Description | PFI-1 (PF-6405761), a specific BET (bromodomain-containing protein) inhibitor for BRD4, is with the IC50 of 0.22 μM in a cell-free assay. |
| Cell Research | To determine dose response, cells are aliquoted into 96-well plate at 5 × 103 cells per well in triplicates. PFI-1 is added by 2- or 4-fold serial dilutions. Cell number is measured 5 days after plating using the CellTiter-Glo Kit and normalized to corresponding vehicle-treated groups. IC50 values are calculated by the GraphPad Prism 5 software using the 4-parameter logistic nonlinear regression model. To calculate the relative growth of cells, averaged cell titers of each group on day 1 are assigned a value of 1. All subsequent cell titer values are normalized accordingly. (Only for Reference) |
| In vitro | In rats, PFI-1, administered intravenously at a dose of 1 mg/kg, exhibits a distribution volume of 1 L/kg and a plasma clearance rate of 18 mL/kg per minute, with a half-life of 1 hour. Orally administered PFI-1 at a dose of 2 mg/kg demonstrates a low efficacy of 32%. When PFI-1 is administered subcutaneously to mice at a 2 mg/kg dose, the peak concentration (Cmax) reaches 58 ng/mL, the time to peak concentration (Tmax) is 1 hour, and the half-life is approximately 2 hours. |
| In vivo | In human monocytes stimulated by lipopolysaccharides, PFI-1 (EC50=1.89 μM) suppresses the production of IL-6. It also inhibits cell proliferation in three NET cell lines (pancreatic NET-derived Bon-1 and lung NET-derived H727 and H720). In T4302 CD133+ cells, PFI-1 induces a dose-dependent decrease in cell viability. PFI-1 (KD=49 μM) binds to the cAMP response element-binding protein. |
| 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 : 40 mg/mL (115.14 mM), Sonication is recommended. |
| Keywords | PFI-1 | PF6405761 | PF 6405761 | Inhibitor | inhibit | EpigeneticReaderDomain | Epigenetic Reader Domain | BRD4 | BRD2 | Autophagy | Apoptosis |
| Inhibitors Related | Stavudine | Cysteamine hydrochloride | Sodium 4-phenylbutyrate | Hydroxychloroquine | Guanidine hydrochloride | Tributyrin | Paeonol | Naringin | L-Ascorbic acid sodium salt | Alginic acid | Gefitinib | Dextran sulfate sodium salt (MW 5000) |
| Related Compound Libraries | Highly Selective Inhibitor Library | Apoptosis Compound Library | Reprogramming Compound Library | Histone Modification Compound Library | Bioactive Compound Library | Chromatin Modification Compound Library | Autophagy Compound Library | Inhibitor Library | NO PAINS Compound Library | PPI Inhibitor Library | Anti-Aging Compound Library | Bioactive Compounds Library Max |
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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