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Lenvatinib

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Primary targets: FLT1_VEGFR1, FLT4_VEGFR3, KDR_VEGFR2, RET · FDA status: FDA Approved

Selectivity scorecard

KISS
97.74
Gini
0.726
CATDS
0.020

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 Lenvatinib. Strongest target: RET at 98.8% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1RET98.8%1.2%
2KDR_VEGFR298.1%1.9%
3FLT4_VEGFR397.4%2.6%
4TNIK97.2%2.8%
5FLT1_VEGFR194.8%5.2%
6DDR294.3%5.7%
7LCK93.4%6.6%
8DDR192.3%7.7%
9RIPK390.6%9.4%
10PDGFRA88.0%12.0%
11P38A_MAPK1487.1%12.9%
12C_KIT86.3%13.7%
13FGFR185.5%14.5%
14FGFR285.4%14.6%
15FMS84.9%15.1%
16FGFR379.9%20.1%
17FGFR479.3%20.7%
18MINK_MINK179.2%20.8%
19SLK_STK277.1%22.9%
20LYN76.6%23.4%

Selectivity landscape

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

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