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Compound Detail

CHEMBL1090526

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COc1nccnc1[C@H](C)C1=C(CCN(C)C)Cc2cc(F)ccc21

Basic Information

ChEMBL ID CHEMBL1090526
Phase Preclinical
Structure Type MOL
InChI Key ABDWUBPDHWDFCV-CYBMUJFWSA-N
4
Targets
6
Activities
2
Assay Types
0
PK Parameters
12
Publications
0
Known Names

Molecular Properties

341.4
MW (Da)
3.69
ALogP
4
HBA
0
HBD
38.2
PSA (Ų)
0.80
QED
0
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H24FN3O
MW 341.43
Aromatic Rings 2
Heavy Atoms 25
NP-Likeness -0.50

Activity Summary

IC50 3 meas. best 5.75
Ki 3 meas. best 9.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL231
Ki 9.15 9.15 0.7 2
Histamine H2 receptor
CHEMBL1941
Ki 8.35 8.35 4.5 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.75 5.75 1800.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.19 5.19 6400.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20800486 10.1016/j.bmcl.2010.07.117 Unchecked 5
20227880 10.1016/j.bmcl.2010.02.055 Voltage-gated inwardly rectifying potassium channel KCNH2 2
20227880 10.1016/j.bmcl.2010.02.055 Histamine H1 receptor 1
20227880 10.1016/j.bmcl.2010.02.055 Muscarinic acetylcholine receptor M1 1
20227880 10.1016/j.bmcl.2010.02.055 Cytochrome P450 2D6 1
20227880 10.1016/j.bmcl.2010.02.055 Cytochrome P450 3A4 1
20227880 10.1016/j.bmcl.2010.02.055 Unchecked 1
20800486 10.1016/j.bmcl.2010.07.117 Cytochrome P450 2D6 1
20800486 10.1016/j.bmcl.2010.07.117 Cytochrome P450 3A4 1
20800486 10.1016/j.bmcl.2010.07.117 Histamine H1 receptor 1
20800486 10.1016/j.bmcl.2010.07.117 Histamine H2 receptor 1
20800486 10.1016/j.bmcl.2010.07.117 Hepatocyte 1

Data from ChEMBL 36 via Core Engine