| Company Name: |
Sigma-Aldrich
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| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
| Products Intro: |
Product Name:PIP3 Antagonist II, DM-PIT-1 - CAS 701947-53-7 - Calbiochem
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| Company Name: |
Shanghai Hongye Biotechnology Co. Ltd
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| Tel: |
400-9205774 |
| Email: |
sales@glpbio.cn |
| Products Intro: |
Product Name:3,5-dimethyl PIT-1
CAS:701947-53-7
Purity:>98% Package:1mg;10mg;50mg;100mg;
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| Company Name: |
DC Chemicals
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| Tel: |
021-58447131 13564518121 |
| Email: |
sales@dcchemicals.com |
| Products Intro: |
Product Name:DM-PIT-1
CAS:701947-53-7
Purity:98% HPLC Package:100mg，250mg，1g
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| | 3,5-dimethyl PIT-1 Basic information |
| Product Name: | 3,5-dimethyl PIT-1 | | Synonyms: | 3,5-dimethyl PIT-1;N-[(2-hydroxy-5-nitrophenyl)carbamothioyl]-3,5-dimethylbenzamide;DM-PIT-1
(3,5-dimethyl PIT-1);PIP3 Antagonist II, DM-PIT-1 - CAS 701947-53-7 - Calbiochem;Benzamide, N-[[(2-hydroxy-5-nitrophenyl)amino]thioxomethyl]-3,5-dimethyl-;DM-PIT-1;3,5 dimethyl PIT 1,3,5dimethyl PIT1 | | CAS: | 701947-53-7 | | MF: | C16H15N3O4S | | MW: | 345.37 | | EINECS: | | | Product Categories: | | | Mol File: | 701947-53-7.mol |  |
| | 3,5-dimethyl PIT-1 Chemical Properties |
| storage temp. | +2C to +8C | | solubility | DMF:30.0(Max Conc. mg/mL);86.86(Max Conc. mM)
DMF:PBS (pH 7.2) (1:1):0.5(Max Conc. mg/mL);1.45(Max Conc. mM)
DMSO:20.0(Max Conc. mg/mL);57.91(Max Conc. mM)
Ethanol:0.2(Max Conc. mg/mL);0.58(Max Conc. mM) | | form | Off-white powder |
| | 3,5-dimethyl PIT-1 Usage And Synthesis |
| Description | PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer. 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorable solubility in vivo. 3,5-dimethyl PIT-1 inhibits PI3K/Akt signaling (IC50 = 27 μM), suppressing PI3K-PDK1-Akt-dependent phosphorylation, which has been shown to reduce cell viability and induce apoptosis in PTEN-deficient U87MG glioblastoma cells (IC50 = 36 μM). 4T1 breast cancer growth is significantly attenuated in BALB/c mice with a dose of 1 mg/kg of 3,5-dimethyl PIT-1 per day. | | General Description | A cell-permeable benzoylthiourea compound that is shown to compete against PIP3 (Cat. No. 524615) for binding PH domains of Akt1 (IC50 ≥31 μM), ARNO, GRP1, and PKD1. Effectively blocks PIP3-dependent cellular PI3K-PDK1-Akt signaling pathway activation in U87MG (25 to 100 μM for 3 d) and PDGF-induced Akt and GRP membrane translocation in serum-starved SUM159 cells (1 h 100 μM pretreatment), while being inactive against PDGF-induced Btk translocation or PMA-induced PLC-δ and TAPP1/2 translocations. Although DM-PIT-1 can be administered as a DMSO stock for effective culture treatments, incorporating DM-PIT-1 into PEG-PE mixed micelles enhances its solubility (up to 1 mM) and i.v. dosing limit for more effective in vivo administrations (5% vs. 41% of control 4T1 tumor size in mice via 1 mg/kg micelles-formulated or 0.4 mg/kg free drug daily i.v., respectively). |
| | 3,5-dimethyl PIT-1 Preparation Products And Raw materials |
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