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Compound Detail

CHEMBL5414613

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COc1ccc(/C2=C/C=C(/c3ccccc3)CNC(=O)CCCCCCCCCCCNC(=O)[C@H](C(C)C)NC2=O)cc1

Basic Information

ChEMBL ID CHEMBL5414613
Phase Preclinical
Structure Type MOL
InChI Key SEMSPJCXQSAXRW-WXBJGDKBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

587.8
MW (Da)
6.45
ALogP
4
HBA
3
HBD
96.5
PSA (Ų)
0.38
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H49N3O4
MW 587.81
Aromatic Rings 2
Heavy Atoms 43
NP-Likeness 0.49

Activity Summary

IC50 1 meas. best 9.36

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KBv200
CHEMBL5465447
IC50 9.36 9.36 0.4 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KBv200 IC50 = 0.44 nM 9.36 Reversal of vinorelbine resistance in human KBv200 cells assessed as reduction i... 36728755

Literature References

PubMed DOI Target Context # Activities
36728755 10.1021/acs.jmedchem.2c01424 KBv200 2

Data from ChEMBL 36 via Core Engine