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IHMT-PI3Kδ-372

IHMT-PI3Kδ-372
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Purity:99.54%
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IHMT-PI3Kδ-372

Catalog No. T35530Cas No. 2429889-62-1
IHMT-PI3Kδ-372 is a selective inhibitor of PI3Kδ with an IC50 of 14 nM and can be used in studies about chronic obstructive pulmonary disease.
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Pack SizePriceAvailabilityQuantity
1 mg$46In Stock
5 mg$113In Stock
10 mg$178In Stock
25 mg$294In Stock
50 mg$436In Stock
100 mg$592In Stock
1 mL x 10 mM (in DMSO)$118In Stock
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Product Introduction

Bioactivity
Description
IHMT-PI3Kδ-372 is a selective inhibitor of PI3Kδ with an IC50 of 14 nM and can be used in studies about chronic obstructive pulmonary disease.
In vitro
In Raji cells, IHMT-PI3Kδ-372 (0.03-3 μM) inhibits PI3Kδ-mediated AKT T308 phosphorylation (EC50 = 67 nM).IHMT-PI3Kδ-372 moderately inhibits CYP2C9 (IC50 = 2.7 μM) and no apparently inhibits CYP1A2, CYP2B6, CYP2C19, and CYP3A4 (IC50s > 10 μM)[1].
In vivo
IHMT-PI3Kδ-372 (1-5 mg/kg; inhalation) improves lung function and reduced the inflammatory patterns characteristic of COPD with better forced expiratory volume in FEV1, FVC, and PEF. IHMT-PI3Kδ-372 dose-dependently decreases the inflammatory cell and reduces the abnormally high level of leukocytes including the alveolar macrophages, neutrophils, and lymphocytes. In rats, IHMT-PI3Kδ-372 (5 mg/kg; inhalation) displays a half-life of 2.3 h, low exposure of 66 ng/mL, and high clearance of 348.5 mL/min/kg in plasma and high exposure of 5599 ng/g (6 h after inhalation) in lung tissue[1].
AliasIHMT-PI3Kδ-372
Chemical Properties
Molecular Weight503.5
FormulaC26H23F2N7O2
Cas No.2429889-62-1
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 37.8 mg/mL (75.1 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9861 mL9.9305 mL19.8610 mL99.3049 mL
5 mM0.3972 mL1.9861 mL3.9722 mL19.8610 mL
10 mM0.1986 mL0.9930 mL1.9861 mL9.9305 mL
20 mM0.0993 mL0.4965 mL0.9930 mL4.9652 mL
50 mM0.0397 mL0.1986 mL0.3972 mL1.9861 mL

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