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Compound Detail

CHEMBL1241641

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Cc1ccc2c(N3CCN(CCc4cccc5c4OCc4nc(C(F)(F)F)cn4-5)CC3)cccc2n1

Basic Information

ChEMBL ID CHEMBL1241641
Phase Preclinical
Structure Type MOL
InChI Key SKGSBVPKDPLIEF-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
2
PK Parameters
8
Publications
0
Known Names

Molecular Properties

493.5
MW (Da)
5.00
ALogP
6
HBA
0
HBD
46.4
PSA (Ų)
0.40
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H26F3N5O
MW 493.53
Aromatic Rings 4
Heavy Atoms 36
NP-Likeness -1.02

Activity Summary

Ki 5 meas. best 9.9

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1D
CHEMBL1983
Ki 9.9 9.9 0.1 1
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 9.8 9.8 0.2 1
5-hydroxytryptamine receptor 1B
CHEMBL1898
Ki 9.0 9.0 1.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 7.6 7.6 25.1 1
Sodium-dependent serotonin transporter
CHEMBL228
Ki 7.5 7.5 31.6 1

Pharmacokinetic Data

Parameter Value Units Species
CL 0.6 mL.min-1.g-1 Rattus norvegicus
CL 1.1 mL.min-1.g-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20590088 10.1021/jm100482n 5-hydroxytryptamine receptor 1A 2
20590088 10.1021/jm100482n 5-hydroxytryptamine receptor 1B 2
20590088 10.1021/jm100482n 5-hydroxytryptamine receptor 1D 2
20590088 10.1021/jm100482n Liver microsomes 2
20590088 10.1021/jm100482n Sodium-dependent serotonin transporter 1
20590088 10.1021/jm100482n Voltage-gated inwardly rectifying potassium channel KCNH2 1
20590088 10.1021/jm100482n Cytochrome P450 2C9 1
20590088 10.1021/jm100482n Cytochrome P450 3A4 1

Data from ChEMBL 36 via Core Engine