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Compound Detail

CHEMBL5265998

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O=C(N[C@H]1C[C@@H]1c1ccc(F)cc1)[C@@H]1CN(C(=O)c2ccc(C(=O)N3C[C@@H](C(=O)N[C@H]4C[C@@H]4c4ccc(F)cc4)[C@H](C(=O)N[C@@H]4C[C@H]4c4ccc(F)cc4)C3)cc2)C[C@H]1C(=O)N[C@H]1C[C@@H]1c1ccc(F)cc1

Basic Information

ChEMBL ID CHEMBL5265998
Phase Preclinical
Structure Type MOL
InChI Key UCXMATXWZYMRHZ-FKGARJMKSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

981.1
MW (Da)
6.31
ALogP
6
HBA
4
HBD
157.0
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 C56H52F4N6O6
MW 981.06
Aromatic Rings 5
Heavy Atoms 72
NP-Likeness -0.41

Activity Summary

EC50 2 meas. best 9.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Toll-like receptor 1/2
CHEMBL3885643
EC50 9.89 9.405 0.1 2

Activity Data Samples

Top measurements by pChEMBL value

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