3,5-dimethyl PIT-1
- Product Name
- 3,5-dimethyl PIT-1
- CAS No.
- 701947-53-7
- Chemical Name
- 3,5-dimethyl PIT-1
- Synonyms
- DM-PIT-1;3,5-dimethyl PIT-1;DM-PIT-1 (3,5-dimethyl PIT-1);3,5 dimethyl PIT 1,3,5dimethyl PIT1;3,5-dimethyl PIT-1, PIP3/protein binding inhibitor;PIP3 Antagonist II, DM-PIT-1 - CAS 701947-53-7 - Calbiochem;N-[(2-hydroxy-5-nitrophenyl)carbamothioyl]-3,5-dimethylbenzamide;Benzamide, N-[[(2-hydroxy-5-nitrophenyl)amino]thioxomethyl]-3,5-dimethyl-
- CBNumber
- CB42590015
- Molecular Formula
- C16H15N3O4S
- Formula Weight
- 345.37
- MOL File
- 701947-53-7.mol
3,5-dimethyl PIT-1 Property
- 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
N-Bromosuccinimide Price
- Product number
- 524619
- Product name
- PIP3 Antagonist II, DM-PIT-1 - CAS 701947-53-7 - Calbiochem<br />The PIP3 Antagonist II, DM-PIT-1, also referenced under CAS 701947-53-7, controls the biological activity of PIP3.
- Packaging
- 25mg
- Price
- $251
- Updated
- 2024/03/01
- Product number
- 10727
- Product name
- 3,5-dimethyl PIT-1
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $26
- Updated
- 2024/03/01
- Product number
- 10727
- Product name
- 3,5-dimethyl PIT-1
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $111
- Updated
- 2024/03/01
- Product number
- 10727
- Product name
- 3,5-dimethyl PIT-1
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $195
- Updated
- 2024/03/01
- Product number
- 10727
- Product name
- 3,5-dimethyl PIT-1
- Purity
- ≥98%
- Packaging
- 25mg
- Price
- $426
- Updated
- 2024/03/01
3,5-dimethyl PIT-1 Chemical Properties,Usage,Production
Description
PtdIns-
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
Raw materials
Preparation Products
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