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Repotrectinib

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Primary targets: ROS_ROS1 · FDA status: FDA Approved

Selectivity scorecard

KISS
84.21
Gini
0.608
CATDS
0.008

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 Repotrectinib. Strongest target: ROS_ROS1 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ROS_ROS1100.0%0.0%
2TRKB99.8%0.2%
3TXK99.8%0.2%
4EPHA299.6%0.4%
5ALK99.4%0.6%
6BMX_ETK99.3%0.7%
7DDR199.3%0.7%
8FAK_PTK299.2%0.8%
9ACK199.0%1.0%
10TRKA98.9%1.1%
11TRKC98.9%1.1%
12FGR98.9%1.1%
13LYN98.7%1.3%
14MUSK98.6%1.4%
15LCK98.6%1.4%
16YES_YES198.4%1.6%
17BLK98.4%1.6%
18JAK298.3%1.7%
19DDR298.3%1.8%
20EPHB498.2%1.8%

Selectivity landscape

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

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