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Pacritinib

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Primary targets: JAK2 · FDA status: FDA Approved

Selectivity scorecard

KISS
88.64
Gini
0.452
CATDS
0.006

Computed from wild-type kinome inhibition at 1 μM. Gini reproduces the published values within tolerance; KISS and CATDS are computed but pending reconciliation with the paper's reference code.

Polypharmacology radar

Top 20 strongest-inhibited wild-type kinases for Pacritinib. Strongest target: IRAK1 at 99.6% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1IRAK199.6%0.4%
2TNIK99.2%0.8%
3CLK198.8%1.2%
4TYK298.8%1.2%
5JAK298.4%1.6%
6LCK98.4%1.6%
7C_KIT98.4%1.6%
8ROS_ROS198.2%1.8%
9CDK9_CYCLIN_K98.0%2.0%
10CDK9_CYCLIN_T297.9%2.1%
11HIPK297.4%2.6%
12HGK_MAP4K497.1%2.9%
13ALK1_ACVRL196.9%3.1%
14CDK9_CYCLIN_T196.8%3.2%
15TRKC96.7%3.3%
16ALK2_ACVR196.7%3.4%
17PKCA96.4%3.6%
18HIPK496.2%3.8%
19FMS95.7%4.3%
20MINK_MINK195.1%4.9%

Selectivity landscape

Where Pacritinib sits in the 92-drug selectivity landscape (KISS vs Gini). The highlighted point is Pacritinib.

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