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Ripretinib

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Primary targets: C_KIT, PDGFRA, PDGFRB · FDA status: FDA Approved

Selectivity scorecard

KISS
92.95
Gini
0.674
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 Ripretinib. Strongest target: ARAF at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ARAF100.0%0.0%
2BRAF100.0%0.0%
3RAF1100.0%0.0%
4C_KIT99.3%0.7%
5YSK4_MAP3K1998.7%1.3%
6ZAK_MLTK97.4%2.6%
7LCK97.2%2.8%
8FMS97.2%2.9%
9DDR196.9%3.1%
10EPHB196.5%3.5%
11TAOK2_TAO196.4%3.6%
12JAK196.0%4.0%
13LYN95.3%4.7%
14HIPK495.3%4.7%
15EPHA295.2%4.8%
16EPHB495.2%4.8%
17DDR294.8%5.2%
18MLK2_MAP3K1094.7%5.3%
19ABL2_ARG94.5%5.5%
20EPHA694.1%5.9%

Selectivity landscape

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

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