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Compound Detail

CHEMBL560923

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CC1=C(c2ccc(OCCCN3CCCC3)cc2)Oc2ccccc2S1

Basic Information

ChEMBL ID CHEMBL560923
Phase Preclinical
Structure Type MOL
InChI Key DREYZGCIOLBBDK-UHFFFAOYSA-N
2
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

367.5
MW (Da)
5.42
ALogP
4
HBA
0
HBD
21.7
PSA (Ų)
0.64
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H25NO2S
MW 367.51
Aromatic Rings 2
Heavy Atoms 26
NP-Likeness -0.80

Activity Summary

IC50 3 meas. best 8.36
Ki 1 meas. best 8.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 8.36 8.36 4.4 2
Histamine H3 receptor
CHEMBL264
IC50 8.07 8.07 8.6 1
Histamine H3 receptor
CHEMBL264
Ki 8.05 8.05 9.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19520574 10.1016/j.bmcl.2009.05.101 Histamine H3 receptor 1
19520574 10.1016/j.bmcl.2009.05.101 Voltage-gated inwardly rectifying potassium channel KCNH2 1
21802950 10.1016/j.bmcl.2011.07.006 No relevant target 1
21802950 10.1016/j.bmcl.2011.07.006 Histamine H3 receptor 1
21802950 10.1016/j.bmcl.2011.07.006 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine