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Compound Detail

CHEMBL1091774

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C[C@@H](c1ccccn1)c1c(CCN2CCCC2)sc2ccccc12

Basic Information

ChEMBL ID CHEMBL1091774
Phase Preclinical
Structure Type MOL
InChI Key GDVOQNXWYQVYJH-INIZCTEOSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

336.5
MW (Da)
5.09
ALogP
3
HBA
0
HBD
16.1
PSA (Ų)
0.65
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C21H24N2S
MW 336.50
Aromatic Rings 3
Heavy Atoms 24
NP-Likeness -1.34

Activity Summary

IC50 2 meas. best 5.57
Ki 2 meas. best 8.24

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Muscarinic acetylcholine receptor M1
CHEMBL216
Ki 8.24 8.24 5.8 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 5.96 5.96 1100.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.57 5.57 2700.0 1
Histamine H1 receptor
CHEMBL231
IC50 5.21 5.21 6100.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20188547 10.1016/j.bmcl.2010.01.134 Voltage-gated inwardly rectifying potassium channel KCNH2 2
20188547 10.1016/j.bmcl.2010.01.134 Histamine H1 receptor 1
20188547 10.1016/j.bmcl.2010.01.134 Muscarinic acetylcholine receptor M1 1
20188547 10.1016/j.bmcl.2010.01.134 Cytochrome P450 2D6 1
20188547 10.1016/j.bmcl.2010.01.134 Cytochrome P450 3A4 1

Data from ChEMBL 36 via Core Engine