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Compound Detail

CHEMBL5573889

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CN1C(=O)[C@@]2(c3cc(Cl)ccc31)[C@H](c1ccccc1)[C@H]1C(=O)c3cc([N+](=O)[O-])ccc3[C@H]1[C@@H]2C(=O)NC(C)(C)C

Basic Information

ChEMBL ID CHEMBL5573889
Phase Preclinical
Structure Type MOL
InChI Key DVQJOXMENFQLEJ-WLQDXNQPSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

558.0
MW (Da)
5.39
ALogP
5
HBA
1
HBD
109.6
PSA (Ų)
0.34
QED
2
Ro5 Violations
3
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H28ClN3O5
MW 558.03
Aromatic Rings 3
Heavy Atoms 40
NP-Likeness -0.42

Activity Summary

IC50 1 meas. best 8.06

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Eca-109/VCR
CHEMBL6066735
IC50 8.06 8.06 8.8 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Eca-109/VCR IC50 = 8.8 nM 8.06 Reversal of vincristine resistance in human Eca-109/VCR cells assessed as vincri... 38784466

Literature References

PubMed DOI Target Context # Activities
38784466 10.1039/d4md00136b Eca-109/VCR 4

Data from ChEMBL 36 via Core Engine