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Baricitinib

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Primary targets: JAK1, JAK2 · FDA status: FDA Approved

Selectivity scorecard

KISS
97.99
Gini
0.616
CATDS
0.014

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 Baricitinib. Strongest target: STK38L_NDR2 at 99.4% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1STK38L_NDR299.4%0.6%
2JAK198.1%1.9%
3TYK297.3%2.7%
4JAK297.2%2.8%
5STK38_NDR197.1%2.9%
6JAK397.0%3.0%
7STK22D_TSSK191.7%8.3%
8PKA90.9%9.1%
9PKCG88.2%11.8%
10LATS186.4%13.6%
11CAMK2D82.2%17.8%
12DAPK181.9%18.1%
13ROCK181.7%18.3%
14DMPK281.2%18.9%
15PKACB80.3%19.7%
16PKACG79.9%20.1%
17ACK179.5%20.5%
18PKCD76.9%23.1%
19ROCK276.5%23.5%
20P70S6K_RPS6KB174.7%25.3%

Selectivity landscape

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

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