KIRhub 2.0
Sign inResearch Use Only

Tivozanib

Sign in to save this workspace

Primary targets: KDR_VEGFR2 · FDA status: FDA Approved

Selectivity scorecard

KISS
92.42
Gini
0.673
CATDS
0.012

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 Tivozanib. Strongest target: RET at 99.7% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1RET99.7%0.3%
2C_KIT99.4%0.6%
3KDR_VEGFR299.3%0.7%
4FLT4_VEGFR399.3%0.7%
5LYN99.3%0.7%
6DDR299.3%0.7%
7FMS98.6%1.4%
8EPHA698.3%1.7%
9EPHB298.0%2.0%
10C_MET97.7%2.4%
11FLT1_VEGFR197.6%2.4%
12LCK97.5%2.5%
13BRK97.2%2.8%
14FRK_PTK597.2%2.8%
15HCK97.1%2.9%
16DDR197.1%2.9%
17PDGFRA96.9%3.1%
18FGR96.6%3.4%
19LOK_STK1096.2%3.8%
20TRKC96.1%3.9%

Selectivity landscape

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

Annotations

Sign in to read and post annotations.

Loading…