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Compound Detail

CHEMBL5427928

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O=C1CCCCCCCCCCCNC(=O)[C@@H]2CCCN2C(=O)/C(c2ccccc2)=C\C=C(\c2ccccc2)CN1

Basic Information

ChEMBL ID CHEMBL5427928
Phase Preclinical
Structure Type MOL
InChI Key CABGJGFZNGGIMQ-MHKYBSRRSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

555.8
MW (Da)
6.29
ALogP
3
HBA
2
HBD
78.5
PSA (Ų)
0.46
QED
2
Ro5 Violations
2
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H45N3O3
MW 555.76
Aromatic Rings 2
Heavy Atoms 41
NP-Likeness 0.23

Activity Summary

IC50 1 meas. best 8.06

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KBv200
CHEMBL5465447
IC50 8.06 8.06 8.6 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KBv200 IC50 = 8.63 nM 8.06 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