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Duvelisib

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Primary targets: PI3K · FDA status: FDA Approved

Selectivity scorecard

KISS
100.00
Gini
0.716
CATDS
0.030

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 Duvelisib. Strongest target: PDK2_PDHK2 at 42.7% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1PDK2_PDHK242.7%57.3%
2CAMKK234.4%65.6%
3DNA_PK33.4%66.6%
4PKG2_PRKG233.3%66.7%
5VRK124.2%75.8%
6P38A_MAPK1421.9%78.1%
7LYN21.7%78.3%
8STK39_STLK321.6%78.4%
9PKMYT120.3%79.7%
10GSK3A18.7%81.3%
11AURORA_C18.6%81.4%
12HASPIN18.5%81.5%
13CDK2_CYCLIN_A118.2%81.8%
14MUSK18.2%81.8%
15MEKK317.6%82.4%
16ITK17.5%82.5%
17ROS_ROS116.5%83.5%
18EPHA415.8%84.2%
19PKCTHETA15.4%84.6%
20PDK1_PDPK115.2%84.8%

Selectivity landscape

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

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