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Ponatinib

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Primary targets: BCR_ABL, ABL1, ABL2_ARG · FDA status: FDA Approved

Selectivity scorecard

KISS
78.23
Gini
0.534
CATDS
0.007

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 Ponatinib. Strongest target: ABL1 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ABL1100.0%0.0%
2ABL2_ARG100.0%0.0%
3BLK100.0%0.0%
4C_KIT100.0%0.0%
5DDR2100.0%0.0%
6EPHA6100.0%0.0%
7FLT1_VEGFR1100.0%0.0%
8LYN100.0%0.0%
9LYN_B100.0%0.0%
10NEK4100.0%0.0%
11PDGFRB100.0%0.0%
12RAF1100.0%0.0%
13RET100.0%0.0%
14SRMS100.0%0.0%
15PDGFRA100.0%0.0%
16EPHB2100.0%0.0%
17C_SRC99.8%0.2%
18HCK99.8%0.2%
19FLT4_VEGFR399.8%0.2%
20HPK1_MAP4K199.7%0.3%

Selectivity landscape

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

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