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Compound Detail

CHEMBL368816

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N#Cc1ccc(S(=O)(=O)C2(F)CCN(CCc3ccc(F)cc3F)CC2)cc1

Basic Information

ChEMBL ID CHEMBL368816
Phase Preclinical
Structure Type MOL
InChI Key RPBDTRSLAXVOEM-UHFFFAOYSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

408.4
MW (Da)
3.61
ALogP
4
HBA
0
HBD
61.2
PSA (Ų)
0.76
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C20H19F3N2O2S
MW 408.45
Aromatic Rings 2
Heavy Atoms 28
NP-Likeness -1.59

Activity Summary

Ki 5 meas. best 8.88

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL322
Ki 8.88 8.88 1.3 1
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 8.57 8.57 2.7 1
D(2) dopamine receptor
CHEMBL217
Ki 6.06 6.06 863.0 1
5-hydroxytryptamine receptor 2C
CHEMBL225
Ki 5.83 5.83 1491.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 5.57 5.57 2702.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15993598 10.1016/j.bmcl.2005.05.104 5-hydroxytryptamine receptor 2A 3
15993598 10.1016/j.bmcl.2005.05.104 5-hydroxytryptamine receptor 2C 1
15993598 10.1016/j.bmcl.2005.05.104 D(2) dopamine receptor 1
15993598 10.1016/j.bmcl.2005.05.104 Voltage-gated inwardly rectifying potassium channel KCNH2 1
15993598 10.1016/j.bmcl.2005.05.104 No relevant target 1

Data from ChEMBL 36 via Core Engine