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Assay Detail

CHEMBL5137735

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Binding
Inhibition of PKM2 (unknown origin)
15
Total Activities
15
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

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

Target

Pyruvate kinase PKM (CHEMBL1075189)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A Perspective on Medicinal Chemistry Approaches for Targeting Pyruvate Kinase M2.
Arora S, Joshi G, Chaturvedi A, Heuser M, Patil S, Kumar R.
J Med Chem (2022) 65 : 1171 -1205
PubMed 34726055 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Inhibition 9 - -
IC50 6 5.49 6.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL9470 SHIKONIN 1 6.10
CHEMBL28457 ALKANNIN 1 6.05
CHEMBL19612 SPERMIDINE 3.0 1 5.85
CHEMBL214344 1 5.16
CHEMBL32749 FERULATE -1.0 1 4.94
CHEMBL1414 SYRINGIC ACID 1 4.86
CHEMBL301523 PHENYLALANINE 3.0 1 -
CHEMBL279597 ALANINE 3.0 1 -
CHEMBL42336 METHIONINE 3.0 1 -
CHEMBL54922 PROLINE 2.0 1 -
CHEMBL54976 TRYPTOPHAN 4.0 1 -
CHEMBL43068 VALINE 2.0 1 -
CHEMBL1233584 ISOLEUCINE 2.0 1 -
CHEMBL291747 THREONINE 2.0 1 -
CHEMBL863 CYSTEINE 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL9470 SHIKONIN IC50 = 800.0 nM 6.10
CHEMBL28457 ALKANNIN IC50 = 900.0 nM 6.05
CHEMBL19612 SPERMIDINE IC50 = 1410.0 nM 5.85
CHEMBL214344 IC50 = 7000.0 nM 5.16
CHEMBL32749 FERULATE IC50 = 11400.0 nM 4.94
CHEMBL1414 SYRINGIC ACID IC50 = 13800.0 nM 4.86
CHEMBL301523 PHENYLALANINE Inhibition = 100.0 % -
CHEMBL279597 ALANINE Inhibition = 100.0 % -
CHEMBL42336 METHIONINE Inhibition = 65.0 % -
CHEMBL54922 PROLINE Inhibition = 65.0 % -
CHEMBL54976 TRYPTOPHAN Inhibition = 65.0 % -
CHEMBL43068 VALINE Inhibition = 65.0 % -
CHEMBL1233584 ISOLEUCINE Inhibition = 20.0 % -
CHEMBL291747 THREONINE Inhibition = 20.0 % -
CHEMBL863 CYSTEINE Inhibition = 20.0 % -