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Compound Detail

CHEMBL453757

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CCCCCC[C@@H]1C(=O)N[C@H]([C@H](O)C(C)C)C(=O)N[C@H]([C@@H](C)CC)C(=O)N(C)[C@@H](C)C(=O)N(C)[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N(C)[C@@H](C)C(=O)N1C

Basic Information

ChEMBL ID CHEMBL453757
Phase Preclinical
Structure Type BOTH
InChI Key JPBLSECMQZGPKF-ZBADXXHPSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

808.1
MW (Da)
2.93
ALogP
8
HBA
4
HBD
188.8
PSA (Ų)
0.20
QED
1
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H77N7O8
MW 808.12
Aromatic Rings 0
Heavy Atoms 57
NP-Likeness 1.15

Activity Summary

IC50 2 meas. best 7.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3T3-L1
CHEMBL614510
IC50 7.8 7.49 16.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
3T3-L1 IC50 = 16.0 nM 7.8 Inhibition of fat accumulation in mouse 3T3L1 cells assessed as liberated trigly... 18798610
3T3-L1 IC50 = 66.0 nM 7.18 Toxicity in mouse 3T3L1 cells 18798610

Literature References

PubMed DOI Target Context # Activities
18798610 10.1021/jm800741n 3T3-L1 2

Data from ChEMBL 36 via Core Engine