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Compound Detail

CHEMBL4084325

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CCCCc1cc(OC2CCN(CCCS(=O)(=O)C(C)(C)C)CC2)c2ncccc2c1

Basic Information

ChEMBL ID CHEMBL4084325
Phase Preclinical
Structure Type MOL
InChI Key HSINSDXPTLWBKS-UHFFFAOYSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

446.7
MW (Da)
5.02
ALogP
5
HBA
0
HBD
59.5
PSA (Ų)
0.54
QED
1
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H38N2O3S
MW 446.66
Aromatic Rings 2
Heavy Atoms 31
NP-Likeness -0.57

Activity Summary

IC50 1 meas. best 6.33
Kd 1 meas. best 9.58

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL231
Kd 9.58 9.58 0.3 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.33 6.33 467.7 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
28958623 10.1016/j.bmcl.2017.09.020 Histamine H1 receptor 2
28958623 10.1016/j.bmcl.2017.09.020 Voltage-gated inwardly rectifying potassium channel KCNH2 1
28958623 10.1016/j.bmcl.2017.09.020 No relevant target 1
28958623 10.1016/j.bmcl.2017.09.020 ADMET 1
28958623 10.1016/j.bmcl.2017.09.020 Brain 1

Data from ChEMBL 36 via Core Engine