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Bosutinib

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

Selectivity scorecard

KISS
87.22
Gini
0.555
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 Bosutinib. Strongest target: ACK1 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ACK1100.0%0.0%
2BLK100.0%0.0%
3C_SRC100.0%0.0%
4FRK_PTK5100.0%0.0%
5KHS_MAP4K5100.0%0.0%
6MINK_MINK1100.0%0.0%
7HGK_MAP4K4100.0%0.0%
8ERBB4_HER499.9%0.1%
9EPHB299.8%0.2%
10ABL199.7%0.3%
11FYN99.7%0.3%
12EPHA299.7%0.3%
13LCK99.7%0.3%
14TNIK99.6%0.4%
15SIK299.6%0.4%
16EPHA499.6%0.4%
17HCK99.6%0.4%
18EPHB199.5%0.5%
19CSK99.5%0.5%
20BTK99.3%0.7%

Selectivity landscape

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

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