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Compound Detail

CHEMBL447873

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CC[C@H](C)[C@H]1NC(=O)[C@@H](COCc2ccccc2)NC(=O)[C@H](C)N(C)C(=O)[C@H](C)N(C)C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C)N(C)C1=O

Basic Information

ChEMBL ID CHEMBL447873
Phase Preclinical
Structure Type BOTH
InChI Key NSYHQDOGCPSFID-WOPUIYLHSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

786.0
MW (Da)
2.18
ALogP
8
HBA
3
HBD
177.8
PSA (Ų)
0.32
QED
1
Ro5 Violations
10
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H67N7O8
MW 786.03
Aromatic Rings 1
Heavy Atoms 56
NP-Likeness 0.87

Activity Summary

IC50 2 meas. best 5.23

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3T3-L1
CHEMBL614510
IC50 5.23 4.64 5900.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
3T3-L1 IC50 = 5900.0 nM 5.23 Inhibition of fat accumulation in mouse 3T3L1 cells assessed as liberated trigly... 18798610
3T3-L1 IC50 = 89000.0 nM 4.05 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