Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5535186

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of PIM1 (unknown origin)
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Serine/threonine-protein kinase pim-1 (CHEMBL2147)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Comprehensive Insights that Targeting PIM for Cancer Therapy: Prospects and Obstacles.
Chen L, Mao W, Ren C, Li J, Zhang J.
J Med Chem (2024) 67 : 38 -64
PubMed 38164076 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 8.08 9.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5595384 1 9.62
CHEMBL5570349 1 9.05
CHEMBL5595879 1 8.77
CHEMBL4467168 DAPOLSERTIB 2.0 1 8.70
CHEMBL5573588 1 8.52
CHEMBL3975308 NUVISERTIB 2.0 1 8.30
CHEMBL3651966 LGH-447 1.0 1 8.24
CHEMBL1952329 SGI-1776 1.0 1 8.15
CHEMBL5564292 1 7.81
CHEMBL4878958 1 7.65
CHEMBL5199618 1 7.45
CHEMBL5205827 1 7.24
CHEMBL5204548 1 7.09
CHEMBL4869696 1 6.55
CHEMBL1398474 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5595384 IC50 = 0.24 nM 9.62
CHEMBL5570349 IC50 = 0.9 nM 9.05
CHEMBL5595879 IC50 = 1.7 nM 8.77
CHEMBL4467168 DAPOLSERTIB IC50 = 2.0 nM 8.70
CHEMBL5573588 IC50 = 3.0 nM 8.52
CHEMBL3975308 NUVISERTIB IC50 = 5.0 nM 8.30
CHEMBL3651966 LGH-447 IC50 = 5.8 nM 8.24
CHEMBL1952329 SGI-1776 IC50 = 7.0 nM 8.15
CHEMBL5564292 IC50 = 15.4 nM 7.81
CHEMBL4878958 IC50 = 22.27 nM 7.65
CHEMBL5199618 IC50 = 35.13 nM 7.45
CHEMBL5205827 IC50 = 57.34 nM 7.24
CHEMBL5204548 IC50 = 81.49 nM 7.09
CHEMBL4869696 IC50 = 279.0 nM 6.55
CHEMBL1398474 IC50 = 1.28 nM -