KIRhub 2.0
Sign inResearch Use Only

Leniolisib

Sign in to save this workspace

Primary targets: PI3K · FDA status: FDA Approved

Selectivity scorecard

KISS
100.00
Gini
0.604
CATDS
0.017

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 Leniolisib. Strongest target: AKT3 at 27.4% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1AKT327.4%72.6%
2DAPK220.1%79.9%
3SYK19.5%80.5%
4STK3319.2%80.8%
5ALK4_ACVR1B18.6%81.4%
6MAST318.0%82.0%
7MEKK317.2%82.8%
8WNK317.0%83.0%
9CDC7_DBF415.8%84.2%
10ERK115.8%84.2%
11CDK1_CYCLIN_A15.7%84.3%
12PDK3_PDHK315.7%84.3%
13DNA_PK15.6%84.4%
14EPHA615.3%84.7%
15TYRO3_SKY15.2%84.8%
16RAF115.2%84.8%
17CDK6_CYCLIN_D314.3%85.7%
18JNK213.5%86.5%
19ERN1_IRE113.4%86.6%
20PKG1B13.4%86.6%

Selectivity landscape

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

Annotations

Sign in to read and post annotations.

Loading…