KIRhub 2.0
Sign inResearch Use Only

Lapatinib

Sign in to save this workspace

Primary targets: EGFR, ERBB2_HER2 · FDA status: FDA Approved

Selectivity scorecard

KISS
99.25
Gini
0.616
CATDS
0.038

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 Lapatinib. Strongest target: EGFR at 99.2% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1EGFR99.2%0.8%
2ERBB4_HER497.8%2.2%
3ERBB2_HER295.8%4.2%
4RIPK352.5%47.5%
5SLK_STK251.5%48.5%
6ARAF47.3%52.7%
7CAMKK237.0%63.0%
8PKMYT131.1%68.9%
9BRK30.3%69.7%
10RAF129.6%70.4%
11RIPK428.9%71.1%
12ERN1_IRE128.5%71.5%
13TRPM7_CHAK125.7%74.3%
14TLK125.0%75.0%
15PKCNU_PRKD321.9%78.1%
16PDK2_PDHK221.4%78.6%
17HASPIN20.8%79.2%
18NEK820.0%80.0%
19IKKA_CHUK20.0%80.0%
20TTBK219.9%80.1%

Selectivity landscape

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

Annotations

Sign in to read and post annotations.

Loading…