KIRhub 2.0
Sign inResearch Use Only

Tenalisib

Sign in to save this workspace

Primary targets: PI3K · FDA status: FDA Phase I Trials Completed

Selectivity scorecard

KISS
97.98
Gini
0.702
CATDS
0.027

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 Tenalisib. Strongest target: RET at 98.5% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1RET98.5%1.5%
2TRKC98.1%1.9%
3FGFR398.0%2.0%
4JAK196.4%3.6%
5FGFR296.0%4.0%
6TRKB95.3%4.7%
7JAK293.8%6.2%
8FGFR193.2%6.8%
9ROS_ROS187.4%12.6%
10FGFR483.9%16.1%
11FLT376.8%23.2%
12DDR173.4%26.6%
13TRKA59.0%41.0%
14JAK355.1%44.9%
15LIMK154.4%45.6%
16TYK252.3%47.7%
17MLK3_MAP3K1152.0%48.0%
18FLT4_VEGFR348.7%51.3%
19ALK45.2%54.8%
20C_SRC39.0%61.0%

Selectivity landscape

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

Annotations

Sign in to read and post annotations.

Loading…