[CAS NO. 1159824-67-5]  CZC24832

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PRODUCTS SPECIFICATIONS [1159824-67-5]

Fulfillment
Catalog
AS941696
Brand
Arctom Scientific
CAS
1159824-67-5

DESCRIPTION [1159824-67-5]

Overview

MDLMFCD22417090
Molecular Weight364.4
Molecular FormulaC15H17FN6O2S
SMILESFC1=CC(=CN2C1=NC(N)=N2)C=3C=C(S(NC(C)(C)C)(=O)=O)C=NC3

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM2.7442 mL13.7212 mL27.4424 mL
5 mM0.5488 mL2.7442 mL5.4885 mL
10 mM0.2744 mL1.3721 mL2.7442 mL
50 mM---

Description

CZC24832 is the first selective inhibitor with of 27 nM, with 10-fold selectivity over PI3Kβ and >100-fold selectivity over PI3Kα and PI3Kδ.

Targets

PI3Kγ [1]
(Cell-free assay)
PI3Kβ [1]
(Cell-free assay)
27 nM1.1 μM

In vitro

CZC24832 has excellent selectivity to PI3Kγ. Out of the 154 identified lipid and protein kinases and the 922 other proteins, only two off targets (PI3Kβ and PIP4K2C) are detected within a 100-fold selectivity window. Despite the high sequence conservation of the human and rodent class I PI3K isoforms, the potency of CZC24832 for PI3Kγ and PI3Kβ is consistently lower by a factor of 2 to 4 in mice and rats compared to humans, but selectivity windows are largely retained. In the BT system, treatment with CZC24832 results in profound inhibition of IL-17A (IC50 =1.5 μM) as well as of B-cell activation markers such as IL-6 and IgG. In addition, strong inhibition of IL17A production is observed in T-cell systems such as human umbilical vein endothelial cells grown in the presence of TH2 blasts, indicating a general role for PI3Kγ kinase activity in the control of TH17 function. Thus, CZC24832 inhibits TH17 cell differentiation.

In vivo

In an IL-8–dependent air pouch model, CZC24832 shows a dose dependent reduction of granulocyte recruitment consistent with the degree of inhibition observed in PI3Kγ-null mice. In a therapeutic collagen induced arthritis (CIA) model, mice treated orally with 10 mg CZC24832 per kg body weight twice per day shows a substantial decrease of bone and cartilage destruction as well as of overall clinical parameters.


Synonyms

3-Pyridinesulfonamide, 5-(2-amino-8-fluoro[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N-(1,1-dimethylethyl)-
5-(2-Amino-8-fluoro[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N-(1,1-dimethylethyl)-3-pyridinesulfonamide
CZC 24832