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Compound Detail

CHEMBL4639472

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Cc1cc(OCCCNC(=O)CCCCCN2/C(=C\C=C\C=C\C3=[N+](CCCCS(=O)(=O)[O-])c4ccccc4C3(C)C)C(C)(C)c3ccccc32)ccc1-c1nc2c(C)c(F)ccc2[nH]1

Basic Information

ChEMBL ID CHEMBL4639472
Phase Preclinical
Structure Type MOL
InChI Key PVBOICHXQQRFAQ-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

900.2
MW (Da)
10.63
ALogP
7
HBA
2
HBD
130.5
PSA (Ų)
0.03
QED
2
Ro5 Violations
20
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C53H62FN5O5S
MW 900.17
Aromatic Rings 5
Heavy Atoms 65
NP-Likeness -0.50

Activity Summary

Ki 2 meas. best 5.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 5.62 5.62 2398.8 1
Histamine H4 receptor
CHEMBL3759
Ki 5.15 5.15 7079.5 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
32420741 10.1021/acs.jmedchem.0c00160 Histamine H4 receptor 1
32420741 10.1021/acs.jmedchem.0c00160 Histamine H3 receptor 1

Data from ChEMBL 36 via Core Engine