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Compound Detail

CHEMBL4846146

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CC(Oc1cc(Cl)ccc1Cl)c1nc(N)nc(N2CCN(C)CC2)n1

Basic Information

ChEMBL ID CHEMBL4846146
Phase Preclinical
Structure Type MOL
InChI Key YREDDRFGDDZWFS-UHFFFAOYSA-N
4
Targets
9
Activities
1
Assay Types
0
PK Parameters
11
Publications
0
Known Names

Molecular Properties

383.3
MW (Da)
2.65
ALogP
7
HBA
1
HBD
80.4
PSA (Ų)
0.87
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H20Cl2N6O
MW 383.28
Aromatic Rings 2
Heavy Atoms 25
NP-Likeness -1.52

Activity Summary

Ki 9 meas. best 7.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.89 7.53 12.9 4
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 6.45 6.45 355.0 1
D(2) dopamine receptor
CHEMBL217
Ki 6.43 6.43 375.0 2
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 4.82 4.82 15050.0 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
32693296 10.1016/j.ejmech.2020.112529 5-hydroxytryptamine receptor 6 5
32693296 10.1016/j.ejmech.2020.112529 ADMET 2
32693296 10.1016/j.ejmech.2020.112529 5-hydroxytryptamine receptor 7 1
32693296 10.1016/j.ejmech.2020.112529 D(2) dopamine receptor 1
32693296 10.1016/j.ejmech.2020.112529 HepG2 1
37567058 10.1016/j.ejmech.2023.115695 Acetylcholinesterase 1
37567058 10.1016/j.ejmech.2023.115695 Cholinesterase 1
37567058 10.1016/j.ejmech.2023.115695 5-hydroxytryptamine receptor 6 1
37567058 10.1016/j.ejmech.2023.115695 5-hydroxytryptamine receptor 2A 1
37567058 10.1016/j.ejmech.2023.115695 5-hydroxytryptamine receptor 7 1
37567058 10.1016/j.ejmech.2023.115695 D(2) dopamine receptor 1

Data from ChEMBL 36 via Core Engine