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Compound Detail

CHEMBL1222864

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O=C(C1CCN(Cc2ccncc2)CC1)N1CCC(n2c(=O)n(CCN3CCOCC3)c3ccccc32)CC1

Basic Information

ChEMBL ID CHEMBL1222864
Phase Preclinical
Structure Type MOL
InChI Key CULSXUUODLMOSV-UHFFFAOYSA-N
2
Targets
3
Activities
3
Assay Types
3
PK Parameters
8
Publications
0
Known Names

Molecular Properties

532.7
MW (Da)
2.61
ALogP
8
HBA
0
HBD
75.8
PSA (Ų)
0.47
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H40N6O3
MW 532.69
Aromatic Rings 3
Heavy Atoms 39
NP-Likeness -1.55

Activity Summary

IC50 1 meas. best 4.52
Kd 1 meas. best 9.1
Ki 1 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL5076
Ki 9.3 9.3 0.5 1
Histamine H3 receptor
CHEMBL5076
Kd 9.1 9.1 0.8 1
Cytochrome P450 3A4
CHEMBL340
IC50 4.52 4.52 30000.0 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 127.85 ng.hr.mL-1 Rattus norvegicus
CL 10.0 uL.min-1.(10^6cells)-1 Rattus norvegicus
CL 10.0 uL.min-1.(10^6cells)-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20685118 10.1016/j.bmcl.2010.07.052 Histamine H3 receptor 2
20685118 10.1016/j.bmcl.2010.07.052 Hepatocyte 2
20685118 10.1016/j.bmcl.2010.07.052 Cytochrome P450 2C9 1
20685118 10.1016/j.bmcl.2010.07.052 Cytochrome P450 2D6 1
20685118 10.1016/j.bmcl.2010.07.052 Cytochrome P450 3A4 1
20685118 10.1016/j.bmcl.2010.07.052 Cavia porcellus 1
20685118 10.1016/j.bmcl.2010.07.052 Rattus norvegicus 1
20685118 10.1016/j.bmcl.2010.07.052 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine