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Compound Detail

CHEMBL5192180

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CCCCCCCCCCCCCCCC(=O)OC[C@@H](CSC[C@H](N)C(=O)N[C@@H](CO)C(=O)OC)OC(=O)CCCCCCCCCCCCCCC.Cl

Basic Information

ChEMBL ID CHEMBL5192180
Phase Preclinical
Structure Type MOL
InChI Key MGBVNDUTHSYBNT-WBGOJFLJSA-N
Parent Compound CHEMBL5222366
Active Moiety CHEMBL5222366
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

773.2
MW (Da)
9.11
ALogP
10
HBA
3
HBD
154.2
PSA (Ų)
0.03
QED
2
Ro5 Violations
39
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H81ClN2O8S
MW 809.64
Aromatic Rings 0
Heavy Atoms 53
NP-Likeness 0.38

Activity Summary

EC50 1 meas. best 6.87

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
TLR2/TLR6
CHEMBL3301399
EC50 6.87 6.87 133.7 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
TLR2/TLR6 EC50 = 133.7 nM 6.87 Agonist activity at human TLR2/TLR6 expressed in HEK-Blue hTLR2-TLR6 cells by SE... 35694694

Literature References

PubMed DOI Target Context # Activities
35694694 10.1039/d1md00372k TLR2/TLR6 5

Data from ChEMBL 36 via Core Engine