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Compound Detail

CHEMBL1092377

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C[C@@H](c1ncccc1F)c1c(CCN(C)C)sc2ccccc12

Basic Information

ChEMBL ID CHEMBL1092377
Phase Preclinical
Structure Type MOL
InChI Key GETROLYXSDDSDH-CYBMUJFWSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

328.5
MW (Da)
4.69
ALogP
3
HBA
0
HBD
16.1
PSA (Ų)
0.68
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 C19H21FN2S
MW 328.46
Aromatic Rings 3
Heavy Atoms 23
NP-Likeness -1.11

Activity Summary

IC50 2 meas. best 6.48
Ki 2 meas. best 8.57

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL231
Ki 8.57 8.57 2.7 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.48 6.48 330.0 1
Muscarinic acetylcholine receptor M1
CHEMBL216
Ki 5.66 5.66 2200.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.4 5.4 4000.0 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