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Vandetanib

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Primary targets: KDR_VEGFR2 · FDA status: FDA Approved

Selectivity scorecard

KISS
95.74
Gini
0.723
CATDS
0.016

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 Vandetanib. Strongest target: EGFR at 99.3% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1EGFR99.3%0.7%
2LCK98.9%1.1%
3RET98.6%1.4%
4DDR298.5%1.5%
5DDR198.5%1.5%
6LYN98.0%2.0%
7EPHA697.3%2.7%
8ABL195.7%4.3%
9BRK95.3%4.7%
10YES_YES195.2%4.8%
11FLT4_VEGFR394.8%5.2%
12KDR_VEGFR294.5%5.5%
13PEAK194.4%5.6%
14C_SRC94.2%5.8%
15LOK_STK1093.8%6.2%
16BLK92.8%7.2%
17FGFR290.8%9.2%
18ABL2_ARG89.0%11.0%
19FLT1_VEGFR188.6%11.4%
20EPHB188.1%11.9%

Selectivity landscape

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

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