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Compound Detail

CHEMBL457022

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Cc1cc(C)c(-c2cc(-c3ccc(N(C)C)cc3)[s+]c(-c3ccc(N(C)C)cc3)c2)c(C)c1.F[P-](F)(F)(F)(F)F

Basic Information

ChEMBL ID CHEMBL457022
Phase Preclinical
Structure Type MOL
InChI Key MXUJBCDWGVPANJ-UHFFFAOYSA-N
Parent Compound CHEMBL1186280
Active Moiety CHEMBL1186280
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

453.7
MW (Da)
8.09
ALogP
2
HBA
0
HBD
6.5
PSA (Ų)
0.28
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H33F6N2PS
MW 598.64
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -0.25

Activity Summary

IC50 1 meas. best 4.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.15 4.15 71000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 71000.0 nM 4.15 Inhibition of verapamil-induced ATPase activity in lipid activated mouse P-glyco... 18849167

Literature References

PubMed DOI Target Context # Activities
18849167 10.1016/j.bmc.2008.09.065 Unchecked 3
18849167 10.1016/j.bmc.2008.09.065 No relevant target 1

Data from ChEMBL 36 via Core Engine