Home Categories Biochemical Engineering Duvelisib (IPI-145, INK1197)
A5036512

Duvelisib (IPI-145, INK1197) , ≥98% , 1201438-56-3

CAS NO.:1201438-56-3

Empirical Formula: C22H17ClN6O

Molecular Weight: 416.86

MDL number: MFCD15144635

EINECS: 200-256-5

Pack Size Price Stock Quantity
5MG RMB319.20 In Stock
10mg RMB439.20 In Stock
25MG RMB799.20 In Stock
50mg RMB1279.20 In Stock
100MG RMB1898.40 In Stock
1G RMB7180.80 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 205-206o C
Boiling point: 757.8±60.0 °C(Predicted)
Density  1.474±0.06 g/cm3(Predicted)
storage temp.  -20°C
solubility  Soluble in DMSO (up to at least 25 mg/ml)
form  White solid.
pka 10.05±0.10(Predicted)
color  White
Stability: Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.

Description and Uses

Duvelisib (1201438-56-3) is a potent and selective (IC50’s: PI3Kα = 1602nM, PI3Kβ = 85nM, PI3Kδ= 2.5nM, PI3Kγ = 27nM) dual PI3Kδ/γ inhibitor.1 It inhibits B and T cell proliferation, blocks neutrophil migration, and inhibits basophil activation. Duvelisib antagonizes B-cell receptor cross-linking activated pro-survival signals in primary chronic lymphocytic leukemia cells.2?Duvelisib also shows preclinical/clinical activity against other hematologic malignancies such as Non-Hodgkins lymphoma, T-cell lymphoma, and others.3,4?Useful clinical agent for the treatment of various blood cancers. Low-dose treatment of T-cell-inflamed tumor models of head and neck cancers with Duvelisib enhanced responses to PD-L1 blockade via suppression of myeloid-derived suppressor cells.5?Higher doses reversed the effect due to suppression of tumor-infiltrating T lymphocytes

IPI 145 is an 1,2-dihydroisoquinolin-1(2H)-one derivative and has been developed as a modulator of PI3 kinase.

Safety

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H360

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