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Compound Detail

CHEMBL501691

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COC1=C[C@@H](C)[C@@H]2C[C@H]3OC(OC(=O)c4cccc(Cl)c4)[C@H](O)[C@H]4C(C)=C(OC)C(=O)[C@H]([C@@]2(C)C1=O)[C@]43C

Basic Information

ChEMBL ID CHEMBL501691
Phase Preclinical
Structure Type MOL
InChI Key AAHJCAZRAHBCTO-UFUVGSDTSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

545.0
MW (Da)
4.10
ALogP
8
HBA
1
HBD
108.4
PSA (Ų)
0.56
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H33ClO8
MW 545.03
Aromatic Rings 1
Heavy Atoms 38
NP-Likeness 2.34

Activity Summary

IC50 2 meas. best 5.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KB
CHEMBL398
IC50 5.75 5.75 1800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KB IC50 = 1800.0 nM 5.75 Cytotoxicity against human KB cells by microplate method 14640524

Literature References

PubMed DOI Target Context # Activities
14640524 10.1021/np030107a Plasmodium falciparum 1
14640524 10.1021/np030107a KB 1
14640524 10.1021/np030107a Unchecked 1

Data from ChEMBL 36 via Core Engine