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Compound Detail

CHEMBL1290041

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O=c1cc(-c2ccc(C(F)(F)F)cc2)ccn1-c1ccc2c(cnn2CCN2CCCC2)c1

Basic Information

ChEMBL ID CHEMBL1290041
Phase Preclinical
Structure Type MOL
InChI Key RMUWRXSDAOJENI-UHFFFAOYSA-N
3
Targets
3
Activities
2
Assay Types
3
PK Parameters
11
Publications
0
Known Names

Molecular Properties

452.5
MW (Da)
4.97
ALogP
5
HBA
0
HBD
43.1
PSA (Ų)
0.43
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 C25H23F3N4O
MW 452.48
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.65

Activity Summary

IC50 2 meas. best 5.7
Ki 1 meas. best 8.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanin-concentrating hormone receptor 1
CHEMBL344
Ki 8.3 8.3 5.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.7 5.7 2000.0 1
Cytochrome P450 2C19
CHEMBL3622
IC50 4.57 4.57 27000.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 2.0 hr Homo sapiens
T1/2 1.7 hr Rattus norvegicus
T1/2 3.117 hr Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20951036 10.1016/j.bmcl.2010.09.037 Liver microsomes 2
20951036 10.1016/j.bmcl.2010.09.037 Melanin-concentrating hormone receptor 1 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 2C19 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 3A4 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 1A2 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 2B6 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 2C9 1
20951036 10.1016/j.bmcl.2010.09.037 Cytochrome P450 2D6 1
20951036 10.1016/j.bmcl.2010.09.037 ADMET 1
20951036 10.1016/j.bmcl.2010.09.037 No relevant target 1
20951036 10.1016/j.bmcl.2010.09.037 Mus musculus 1

Data from ChEMBL 36 via Core Engine