Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL46512

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
O=C(c1ccc(Cl)c(Cl)c1)N1CCC(F)(CNCc2cccc(-c3nccs3)n2)CC1

Basic Information

ChEMBL ID CHEMBL46512
Phase Preclinical
Structure Type MOL
InChI Key NYFVZSBKYHXQCT-UHFFFAOYSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

479.4
MW (Da)
5.25
ALogP
5
HBA
1
HBD
58.1
PSA (Ų)
0.53
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H21Cl2FN4OS
MW 479.41
Aromatic Rings 3
Heavy Atoms 31
NP-Likeness -1.81

Activity Summary

Ki 3 meas. best 9.1
EC50 1 meas. best 7.64

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL273
Ki 9.1 9.1 0.8 1
5-hydroxytryptamine receptor 1A
CHEMBL214
EC50 7.64 7.64 22.9 1
Adrenergic receptor alpha-1
CHEMBL1907610
Ki 6.26 6.26 549.5 1
D(2) dopamine receptor
CHEMBL339
Ki 5.47 5.47 3388.4 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
10229633 10.1021/jm9806906 Rattus norvegicus 3
10229633 10.1021/jm9806906 5-hydroxytryptamine receptor 1A 2
10229633 10.1021/jm9806906 D(2) dopamine receptor 1
10229633 10.1021/jm9806906 Adrenergic receptor alpha-1 1

Data from ChEMBL 36 via Core Engine