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PI-103

Catalog No. T6143   CAS 371935-74-9
Synonyms: PI103, PI 103

PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of PI3K family members (IC50s: 2/3/3/15/30/23 nM for p110α/β/δ/γ, mTOR, and DNA-PK).

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PI-103 Chemical Structure
PI-103, CAS 371935-74-9
Pack Size Availability Price/USD Quantity
5 mg In stock $ 52.00
10 mg In stock $ 64.00
25 mg In stock $ 126.00
50 mg In stock $ 205.00
100 mg In stock $ 378.00
200 mg In stock $ 576.00
1 mL * 10 mM (in DMSO) In stock $ 54.00
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Purity: 99.3%
Purity: 97.82%
Purity: 96.59%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of PI3K family members (IC50s: 2/3/3/15/30/23 nM for p110α/β/δ/γ, mTOR, and DNA-PK).
Targets&IC50 mTOR:30 nM (cell free), p110α:2 nM (cell free), p110γ:15 nM (cell free), DNA-PK:23 nM (cell free), p110δ:3 nM (cell free), p110β:3 nM (cell free)
In vitro PI-103 potently inhibited p110α (IC50: 15 nmol/L. PI-103 exhibited potent growth inhibition in each of the cell lines examined, with activity in the submicromolar range [1]. PI-103 induced proliferative arrest in a panel of glioma cell lines assayed by flow cytometry. PI-103 uniquely and potently inhibits both complexes of mTOR: the rapamycin-sensitive mTORC1 (IC50: 0.02 μM) and the rapamycin-insensitive mTORC2 (IC50: 0.083 μM). PI-103 (IC50 < 0.1 μM) was blocking the phosphorylation of p70 S6 kinase, ribosomal protein S6, and 4E-BP1, downstream markers of mTOR signaling [2].
In vivo When tumors reached 50–100 mm^3, animals were randomized and treated with vehicle or PI-103. PI-103 showed significant activity in vivo, reducing average tumor size by 4-fold after 18 days. Preclinical treatment of glioma xenografts with PI-103 blocked proliferation without inducing apoptosis [2]. PI-103 (10 mg/kg) treatment promoted a significant in vivo tumor growth compared with the DMSO treated mice. PI-103 (70 mg/kg) also promoted a significant in vivo tumor growth [3].
Kinase Assay Phosphatidylinositide 3-kinase inhibitory activity was determined using a scintillation proximity assay in the presence of 1 μmol/L ATP. Inhibition of mTOR protein kinase was determined using a TR-FRET-based LanthaScreen method. Compounds were assayed at a maximum concentration of 10 μmol/L in the presence of 1 μmol/L ATP, and IC50 values were determined using GraphPad Prism software [1].
Cell Research Human glioma cell lines were obtained from the Brain Tumor Research Center at UCSF. Cells were harvested and fixed, treated with RNAase and propidium iodide, and filtered through 95 mM nylon mesh. Ten thousand stained nuclei were analyzed in a FACS Calibur flow cytometer. DNA histograms were modeled offline using Modifit-LT software. For crystal violet staining, 10^5 cells were seeded in 12-well plates in the presence or absence of PI-103 [2].
Animal Research Five to six-month-old males of either FVB/N strain or nude BALB/c strain were injected subcutaneously with one million cells in PBS. When the tumor reached between 50 and 100 mm^3, mice were treated with the inhibitors. Treatments were done by IP injection daily with 10 mg/kg or 70 mg/kg of PI-103 and/or 50 mg/kg sorafenib. Control mice were treated with the same volume of DMSO. Tumor size and mice weight was monitored every 2 days. Tumor volume was calculated with the equation (d^2*D) (p/6). When mice were sacrificed, tumors were dissected and processed. For immunosuppression experiments, mice were treated with rapamycin (1 mg/kg) or LY294002 (25 mg/kg) by a daily IP injection for a total of 8 days [3].
Synonyms PI103, PI 103
Molecular Weight 348.36
Formula C19H16N4O3
CAS No. 371935-74-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: < 1 mg/mL (insoluble or slightly soluble)

DMSO: 23 mg/mL (66 mM)

TargetMolReferences and Literature

1. Raynaud FI, et al. Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941. Mol Cancer Ther. 2009 Jul;8(7):1725-38. 2. Fan QW, et al. A dual PI3 kinase/mTOR inhibitor reveals emergent efficacy in glioma. Cancer Cell. 2006 May;9(5):341-9. 3. López-Fauqued M, et al. The dual PI3K/mTOR inhibitor PI-103 promotes immunosuppression, in vivo tumor growth and increases survival of sorafenib-treated melanoma cells. Int J Cancer. 2010 Apr 1;126(7):1549-61.

Related compound libraries

This product is contained In the following compound libraries:
Tyrosine Kinase Inhibitor Library Anti-Cancer Active Compound Library Kinase Inhibitor Library Inhibitor Library Anti-Breast Cancer Compound Library Antidepressant Compound Library Autophagy Compound Library Neural Regeneration Compound Library Reprogramming Compound Library Anti-Cancer Metabolism Compound Library

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Keywords

PI-103 371935-74-9 Apoptosis Autophagy DNA Damage/DNA Repair PI3K/Akt/mTOR signaling PI3K mTOR DNA-PK Phosphoinositide 3-kinase Inhibitor PI103 DNA-dependent protein kinase inhibit Mammalian target of Rapamycin PI 103 inhibitor

 

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