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Mitapivat

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Primary targets: PK · FDA status: FDA Approved

Selectivity scorecard

KISS
100.00
Gini
0.625
CATDS
0.028

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 Mitapivat. Strongest target: PDGFRA at 53.3% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1PDGFRA53.3%46.7%
2C_KIT48.1%51.9%
3AURORA_A30.6%69.4%
4PDGFRB26.1%73.9%
5LIMK125.3%74.7%
6PDK3_PDHK323.8%76.3%
7PKD2_PRKD221.2%78.8%
8ASK1_MAP3K520.9%79.1%
9CDK4_CYCLIN_D320.2%79.8%
10DDR119.1%80.9%
11DAPK218.8%81.2%
12MELK18.1%81.9%
13TRKB18.0%82.0%
14CDK9_CYCLIN_T217.9%82.1%
15VRK117.5%82.5%
16LCK17.4%82.6%
17RIPK216.8%83.2%
18AURORA_B16.7%83.3%
19MEKK616.2%83.8%
20MST2_STK315.3%84.7%

Selectivity landscape

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

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