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Sirolimus

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Primary targets: FKBP12, MTOR_FRAP1 · FDA status: FDA Approved

Selectivity scorecard

KISS
100.00
Gini
0.708
CATDS
0.023

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 Sirolimus. Strongest target: ERN1_IRE1 at 31.9% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ERN1_IRE131.9%68.1%
2CAMKK230.4%69.6%
3PKMYT129.5%70.5%
4PDK2_PDHK226.8%73.2%
5WNK124.1%75.9%
6STK21_CIT23.1%76.9%
7MUSK22.9%77.1%
8GSK3A22.3%77.7%
9STK3320.6%79.4%
10PHKG119.8%80.2%
11EGFR18.0%82.0%
12CTK_MATK17.9%82.1%
13MLK3_MAP3K1117.8%82.2%
14TTBK216.0%84.0%
15SLK_STK215.6%84.4%
16STK39_STLK314.9%85.1%
17SSTK_TSSK614.7%85.3%
18TTBK114.2%85.8%
19BMPR213.8%86.2%
20KSR213.2%86.8%

Selectivity landscape

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

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