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Compound Detail

CHEMBL2387260

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Cc1cc(=O)oc2cc(OCCCCN3CCC(c4noc5cc(F)ccc45)CC3)ccc12

Basic Information

ChEMBL ID CHEMBL2387260
Phase Preclinical
Structure Type MOL
InChI Key NAIAJYNMEREGMG-UHFFFAOYSA-N
9
Targets
9
Activities
2
Assay Types
0
PK Parameters
9
Publications
0
Known Names

Molecular Properties

450.5
MW (Da)
5.42
ALogP
6
HBA
0
HBD
68.7
PSA (Ų)
0.28
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 C26H27FN2O4
MW 450.51
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.15

Activity Summary

Ki 8 meas. best 8.46
IC50 1 meas. best 6.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL273
Ki 8.46 8.46 3.5 1
D(2) dopamine receptor
CHEMBL339
Ki 8.31 8.31 4.9 1
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 8.08 8.08 8.4 1
5-hydroxytryptamine receptor 2C
CHEMBL324
Ki 7.92 7.92 11.9 1
Adrenergic receptor alpha-1
CHEMBL1907610
Ki 7.8 7.8 15.8 1
Histamine H1 receptor
CHEMBL3943
Ki 7.71 7.71 19.6 1
D(3) dopamine receptor
CHEMBL3138
Ki 7.15 7.15 71.3 1
Adrenergic receptor alpha-2
CHEMBL2093864
Ki 6.8 6.8 159.6 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.8 6.8 159.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23675993 10.1021/jm400408r Voltage-gated inwardly rectifying potassium channel KCNH2 1
23675993 10.1021/jm400408r Adrenergic receptor alpha-2 1
23675993 10.1021/jm400408r Adrenergic receptor alpha-1 1
23675993 10.1021/jm400408r 5-hydroxytryptamine receptor 2C 1
23675993 10.1021/jm400408r Histamine H1 receptor 1
23675993 10.1021/jm400408r D(3) dopamine receptor 1
23675993 10.1021/jm400408r 5-hydroxytryptamine receptor 2A 1
23675993 10.1021/jm400408r 5-hydroxytryptamine receptor 1A 1
23675993 10.1021/jm400408r D(2) dopamine receptor 1

Data from ChEMBL 36 via Core Engine