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Compound Detail

CHEMBL5076846

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C[C@H]1C[C@H](NS(=O)(=O)c2cc3ccc(F)cc3s2)CN1CCCc1noc2cc(F)ccc12

Basic Information

ChEMBL ID CHEMBL5076846
Phase Preclinical
Structure Type MOL
InChI Key UHSHPGFICACACL-KSSFIOAISA-N
4
Targets
4
Activities
1
Assay Types
2
PK Parameters
9
Publications
0
Known Names

Molecular Properties

491.6
MW (Da)
4.69
ALogP
6
HBA
1
HBD
75.4
PSA (Ų)
0.41
QED
0
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H23F2N3O3S2
MW 491.59
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -1.46

Activity Summary

Ki 4 meas. best 9.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 2A
CHEMBL224
Ki 9.19 9.19 0.6 1
5-hydroxytryptamine receptor 7
CHEMBL3155
Ki 7.31 7.31 49.0 1
D(2) dopamine receptor
CHEMBL217
Ki 7.27 7.27 53.7 1
5-hydroxytryptamine receptor 6
CHEMBL3371
Ki 7.05 7.05 89.1 1

Pharmacokinetic Data

Parameter Value Units Species
CL 610.4 mL.min-1.g-1 Homo sapiens
T1/2 0.1833 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 2A 2
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 6 2
34436892 10.1021/acs.jmedchem.1c00497 5-hydroxytryptamine receptor 7 2
34436892 10.1021/acs.jmedchem.1c00497 D(2) dopamine receptor 2
34436892 10.1021/acs.jmedchem.1c00497 ADMET 2
34436892 10.1021/acs.jmedchem.1c00497 Muscarinic acetylcholine receptor M1 1
34436892 10.1021/acs.jmedchem.1c00497 Histamine H1 receptor 1
34436892 10.1021/acs.jmedchem.1c00497 Alpha-1A adrenergic receptor 1
34436892 10.1021/acs.jmedchem.1c00497 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine