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Compound Detail

CHEMBL2163835

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O=C([C@H](Cc1ccc(Cl)cc1Cl)NC(=O)C1(c2ccc(Cl)cc2Cl)CC1)N1CCNCC1

Basic Information

ChEMBL ID CHEMBL2163835
Phase Preclinical
Structure Type MOL
InChI Key RIJSQWHSYPOPOZ-FQEVSTJZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

515.3
MW (Da)
4.49
ALogP
3
HBA
2
HBD
61.4
PSA (Ų)
0.60
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H23Cl4N3O2
MW 515.27
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness -0.78

Activity Summary

IC50 1 meas. best 6.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Ceramide glucosyltransferase
CHEMBL2063
IC50 6.82 6.82 150.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22497444 10.1021/jm300122u Ceramide glucosyltransferase 2
22497444 10.1021/jm300122u Cytochrome P450 3A4 1
22497444 10.1021/jm300122u ADMET 1

Data from ChEMBL 36 via Core Engine