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Alectinib

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Primary targets: ALK, RET · FDA status: FDA Approved

Selectivity scorecard

KISS
95.49
Gini
0.651
CATDS
0.011

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 Alectinib. Strongest target: SRPK1 at 99.6% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1SRPK199.6%0.4%
2CAMK2D99.5%0.5%
3MSSK1_STK2398.9%1.1%
4CHK298.8%1.2%
5ALK98.6%1.4%
6TYK1_LTK98.2%1.8%
7RET97.8%2.2%
8CAMK2A97.7%2.3%
9PIM395.1%4.9%
10PHKG194.5%5.5%
11LRRK294.5%5.5%
12SRPK294.4%5.6%
13FGR94.2%5.8%
14TRKC94.2%5.8%
15CAMKK293.3%6.7%
16FLT4_VEGFR392.8%7.2%
17LYN92.4%7.6%
18IR91.1%8.9%
19DAPK189.5%10.5%
20PHKG289.3%10.7%

Selectivity landscape

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

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