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Compound Detail

CHEMBL5194860

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CC(CCCc1ccccc1)CNC(=O)/N=C(\N)NCC1CCc2nc(N)sc2C1.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F

Basic Information

ChEMBL ID CHEMBL5194860
Phase Preclinical
Structure Type MOL
InChI Key JEOPVCICUSQEFS-UHFFFAOYSA-N
Parent Compound CHEMBL5222123
Active Moiety CHEMBL5222123
4
Targets
10
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

428.6
MW (Da)
3.10
ALogP
4
HBA
4
HBD
118.4
PSA (Ų)
0.38
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H34F6N6O5S
MW 656.65
Aromatic Rings 2
Heavy Atoms 30
NP-Likeness -0.48

Activity Summary

Kd 5 meas. best 8.52
Ki 5 meas. best 6.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Kd 8.52 8.52 3.0 2
Histamine H1 receptor
CHEMBL231
Kd 8.35 8.35 4.5 1
Histamine H2 receptor
CHEMBL1941
Kd 7.91 7.91 12.2 1
Histamine H4 receptor
CHEMBL3759
Kd 7.8 7.8 16.0 1
Histamine H2 receptor
CHEMBL1941
Ki 6.96 6.96 109.7 1
Histamine H3 receptor
CHEMBL264
Ki 5.76 5.76 1737.8 2
Histamine H1 receptor
CHEMBL231
Ki 5.41 5.41 3890.4 1
Histamine H4 receptor
CHEMBL3759
Ki 5.39 5.39 4073.8 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34110814 10.1021/acs.jmedchem.1c00692 Histamine H3 receptor 4
34110814 10.1021/acs.jmedchem.1c00692 Unchecked 3
34110814 10.1021/acs.jmedchem.1c00692 Histamine H1 receptor 2
34110814 10.1021/acs.jmedchem.1c00692 Histamine H2 receptor 2
34110814 10.1021/acs.jmedchem.1c00692 Histamine H4 receptor 2

Data from ChEMBL 36 via Core Engine