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Compound Detail

CHEMBL5436471

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CCCCC1CN(C(=O)c2ccc(C(=O)N3CC(CCCC)[C@H](C(=O)N[C@H]4C[C@@H]4c4ccccc4)C3)cc2)CC1C(=O)N[C@H]1C[C@@H]1c1ccccc1

Basic Information

ChEMBL ID CHEMBL5436471
Phase Preclinical
Structure Type MOL
InChI Key VOZBXEGXTGAFCR-YBCSGRNESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

702.9
MW (Da)
6.79
ALogP
4
HBA
2
HBD
98.8
PSA (Ų)
0.19
QED
2
Ro5 Violations
14
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H54N4O4
MW 702.94
Aromatic Rings 3
Heavy Atoms 52
NP-Likeness -0.36

Activity Summary

EC50 1 meas. best 5.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Toll-like receptor 2
CHEMBL4163
EC50 5.82 5.82 1500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Toll-like receptor 2 EC50 = 1500.0 nM 5.82 Agonist activity at human TLR2 expressed in HEK-Blue hTLR2 cells as SEAP express... 36174413

Literature References

PubMed DOI Target Context # Activities
36174413 10.1016/j.ejmech.2022.114771 Toll-like receptor 2 1

Data from ChEMBL 36 via Core Engine