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Compound Detail

CHEMBL5200106

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Cc1ccc(CC(C)CNC(=O)/N=C(\N)NCCCc2nnc(N)o2)cc1.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F

Basic Information

ChEMBL ID CHEMBL5200106
Phase Preclinical
Structure Type MOL
InChI Key RDFLIMPCLPMKOW-UHFFFAOYSA-N
Parent Compound CHEMBL5222556
Active Moiety CHEMBL5222556
4
Targets
7
Activities
2
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

373.5
MW (Da)
1.39
ALogP
5
HBA
4
HBD
144.4
PSA (Ų)
0.31
QED
0
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H29F6N7O6
MW 601.51
Aromatic Rings 2
Heavy Atoms 27
NP-Likeness -0.87

Activity Summary

Kd 4 meas. best 8.52
Ki 3 meas. best 6.17

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Kd 8.52 8.52 3.0 1
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 6.17 6.17 676.1 1
Histamine H1 receptor
CHEMBL231
Ki 5.57 5.57 2691.5 1
Histamine H3 receptor
CHEMBL264
Ki 5.04 5.04 9120.1 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
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 H3 receptor 2
34110814 10.1021/acs.jmedchem.1c00692 Histamine H4 receptor 2

Data from ChEMBL 36 via Core Engine