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Compound Detail

CHEMBL4079630

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C#CCCCCCCCCC(=O)OCC[C@@H]1C(=O)NC(=C)/C=C/C(=O)N[C@H](C)C(=O)N[C@@H](C(C)C)C(=O)O[C@H]1[C@H](C)CCCCCC

Basic Information

ChEMBL ID CHEMBL4079630
Phase Preclinical
Structure Type MOL
InChI Key UWWIUAMIEYXBDF-DUMLEDJKSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

657.9
MW (Da)
5.65
ALogP
7
HBA
3
HBD
139.9
PSA (Ų)
0.10
QED
2
Ro5 Violations
18
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H59N3O7
MW 657.89
Aromatic Rings 0
Heavy Atoms 47
NP-Likeness 1.29

Activity Summary

IC50 1 meas. best 5.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
K562
CHEMBL385
IC50 5.36 5.36 4410.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
K562 IC50 = 4410.0 nM 5.36 Cytotoxicity against human K562 cells measured after 72 hrs by MTT assay 28075592

Literature References

PubMed DOI Target Context # Activities
28075592 10.1021/acs.jmedchem.6b01745 K562 2
28075592 10.1021/acs.jmedchem.6b01745 Staphylococcus aureus 1
28075592 10.1021/acs.jmedchem.6b01745 No relevant target 1

Data from ChEMBL 36 via Core Engine