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Compound Detail

CHEMBL5286904

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O=C(N[C@H]1C[C@@H]1c1ccccc1)[C@@H]1CN(C(=O)c2ccc(C(=O)N3C[C@@H](C(=O)N[C@H]4C[C@@H]4c4ccccc4)[C@H](C(=O)N[C@H]4C[C@@H]4c4ccccc4)C3)c(O)c2)C[C@H]1C(=O)N[C@H]1C[C@@H]1c1ccccc1

Basic Information

ChEMBL ID CHEMBL5286904
Phase Preclinical
Structure Type MOL
InChI Key QQFVXDLVQBMRRR-XQXWRADBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

925.1
MW (Da)
5.46
ALogP
7
HBA
5
HBD
177.2
PSA (Ų)
0.10
QED
2
Ro5 Violations
14
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C56H56N6O7
MW 925.10
Aromatic Rings 5
Heavy Atoms 69
NP-Likeness -0.32

Activity Summary

EC50 1 meas. best 7.7

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Toll-like receptor 1/2
CHEMBL3885643
EC50 7.7 7.7 20.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Toll-like receptor 1/2 EC50 = 20.0 nM 7.7 Agonist activity at TLR2/TLR1 in human THP-1 cells 33346636

Literature References

PubMed DOI Target Context # Activities
33346636 10.1021/acs.jmedchem.0c01627 Toll-like receptor 1/2 2

Data from ChEMBL 36 via Core Engine