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Netarsudil

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Primary targets: ROCK1, ROCK2 · FDA status: FDA Approved

Selectivity scorecard

KISS
93.22
Gini
0.676
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 Netarsudil. Strongest target: P70S6K_RPS6KB1 at 99.7% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1P70S6K_RPS6KB199.7%0.3%
2PKCD99.4%0.6%
3ROCK199.3%0.7%
4MSK2_RPS6KA499.1%0.9%
5PRKX98.3%1.7%
6P70S6KB_RPS6KB298.2%1.8%
7PKG1A97.3%2.7%
8PKCEPSILON97.3%2.7%
9PKACB97.2%2.8%
10MSK1_RPS6KA597.1%2.9%
11PKCETA97.0%3.0%
12PKA96.6%3.4%
13RSK396.6%3.4%
14ROCK296.0%4.0%
15STK38_NDR195.8%4.2%
16PKG2_PRKG295.7%4.3%
17PKACG95.4%4.6%
18STK38L_NDR295.0%5.0%
19DMPK294.8%5.2%
20PKD2_PRKD294.6%5.4%

Selectivity landscape

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

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