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Compound Detail

CHEMBL1289614

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CN1CCN(CCCN(C(=O)Nc2ccc(F)c(C(F)(F)F)c2)C2CCC3(c4ccc(C#N)cc4)CC23)CC1

Basic Information

ChEMBL ID CHEMBL1289614
Phase Preclinical
Structure Type MOL
InChI Key QXIJKQBZACKAMG-UHFFFAOYSA-N
2
Targets
2
Activities
2
Assay Types
3
PK Parameters
11
Publications
0
Known Names

Molecular Properties

543.6
MW (Da)
5.31
ALogP
4
HBA
1
HBD
62.6
PSA (Ų)
0.48
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H33F4N5O
MW 543.61
Aromatic Rings 2
Heavy Atoms 39
NP-Likeness -1.19

Activity Summary

IC50 1 meas. best 5.21
Ki 1 meas. best 8.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Melanin-concentrating hormone receptor 1
CHEMBL344
Ki 8.92 8.92 1.2 1
Cytochrome P450 2C19
CHEMBL3622
IC50 5.21 5.21 6100.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.283 hr Homo sapiens
T1/2 1.817 hr Rattus norvegicus
T1/2 9.567 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