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Compound Detail

CHEMBL1092126

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Cc1cccnc1[C@H](C)c1c(CCN(C)C)sc2ccccc12

Basic Information

ChEMBL ID CHEMBL1092126
Phase Preclinical
Structure Type MOL
InChI Key KJQCJXUDPPZASI-OAHLLOKOSA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

324.5
MW (Da)
4.86
ALogP
3
HBA
0
HBD
16.1
PSA (Ų)
0.67
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H24N2S
MW 324.49
Aromatic Rings 3
Heavy Atoms 23
NP-Likeness -0.86

Activity Summary

IC50 2 meas. best 6.04
Ki 1 meas. best 8.03

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL231
Ki 8.03 8.03 9.3 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.04 6.04 910.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.26 5.26 5500.0 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