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Compound Detail

CHEMBL5207928

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

Basic Information

ChEMBL ID CHEMBL5207928
Phase Preclinical
Structure Type MOL
InChI Key IBLLQGMGDOCGRD-KJFLPAQCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

929.4
MW (Da)
12.50
ALogP
11
HBA
2
HBD
155.6
PSA (Ų)
0.03
QED
3
Ro5 Violations
41
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C51H96N2O10S
MW 929.40
Aromatic Rings 0
Heavy Atoms 64
NP-Likeness 0.11

Activity Summary

EC50 1 meas. best 5.37

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
TLR2/TLR6
CHEMBL3301399
EC50 5.37 5.37 4269.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
TLR2/TLR6 EC50 = 4269.0 nM 5.37 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 1

Data from ChEMBL 36 via Core Engine