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Compound Detail

CHEMBL5206630

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

Basic Information

ChEMBL ID CHEMBL5206630
Phase Preclinical
Structure Type MOL
InChI Key TWMUCEFSQRKSOZ-WKSNTLBMSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

815.2
MW (Da)
9.29
ALogP
10
HBA
3
HBD
157.3
PSA (Ų)
0.03
QED
2
Ro5 Violations
40
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H82N2O9S
MW 815.21
Aromatic Rings 0
Heavy Atoms 56
NP-Likeness 0.34

Activity Summary

EC50 1 meas. best 9.1

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
TLR2/TLR6
CHEMBL3301399
EC50 9.1 9.1 0.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
TLR2/TLR6 EC50 = 0.8 nM 9.1 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 Mus musculus 5
35694694 10.1039/d1md00372k TLR2/TLR6 4

Data from ChEMBL 36 via Core Engine