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Compound Detail

CHEMBL203230

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C[C@@H]1CNC[C@H]2Cc3ccc(Cl)nc3N21

Basic Information

ChEMBL ID CHEMBL203230
Phase Preclinical
Structure Type MOL
InChI Key PKOPGQYFQBKBPB-VXNVDRBHSA-N
4
Targets
4
Activities
2
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

223.7
MW (Da)
1.46
ALogP
3
HBA
1
HBD
28.2
PSA (Ų)
0.68
QED
0
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C11H14ClN3
MW 223.71
Aromatic Rings 1
Heavy Atoms 15
NP-Likeness -0.63

Activity Summary

Ki 3 meas. best 8.8
IC50 1 meas. best 4.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2C
CHEMBL225
Ki 8.8 8.8 1.6 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 7.38 7.38 42.0 1
5-hydroxytryptamine receptor 2B
CHEMBL1833
Ki 7.32 7.32 48.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 4.4 4.4 40000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16361098 10.1016/j.bmcl.2005.11.083 5-hydroxytryptamine receptor 2C 2
22122484 10.1021/jm201082a ADMET 2
16361098 10.1016/j.bmcl.2005.11.083 5-hydroxytryptamine receptor 2A 1
16361098 10.1016/j.bmcl.2005.11.083 5-hydroxytryptamine receptor 2B 1
16361098 10.1016/j.bmcl.2005.11.083 Voltage-gated inwardly rectifying potassium channel KCNH2 1
16361098 10.1016/j.bmcl.2005.11.083 Phospholipidosis 1

Data from ChEMBL 36 via Core Engine