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Compound Detail

CHEMBL5400673

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COc1cc(CNC2CCOCC2)ccc1Cn1ncc2nc(N)nc(N[C@@H](C)CCO)c21

Basic Information

ChEMBL ID CHEMBL5400673
Phase Preclinical
Structure Type MOL
InChI Key PUKABMLZTCFSHN-HNNXBMFYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

455.6
MW (Da)
1.92
ALogP
10
HBA
4
HBD
132.4
PSA (Ų)
0.36
QED
0
Ro5 Violations
10
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H33N7O3
MW 455.56
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -0.66

Activity Summary

IC50 1 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Toll-like receptor 7
CHEMBL5936
IC50 6.0 6.0 1003.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Toll-like receptor 7 IC50 = 1003.0 nM 6.0 Agonist activity at human TLR7 in HEK-Blue hTLR7 cells incubated for 18 hrs by Q... 38352830

Literature References

PubMed DOI Target Context # Activities
38352830 10.1021/acsmedchemlett.3c00455 Toll-like receptor 7 2
38352830 10.1021/acsmedchemlett.3c00455 ADMET 2
38352830 10.1021/acsmedchemlett.3c00455 Voltage-gated inwardly rectifying potassium channel KCNH2 1
38352830 10.1021/acsmedchemlett.3c00455 T-cell 1

Data from ChEMBL 36 via Core Engine