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Compound Detail

CHEMBL2402300

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CC(=O)O[C@H]1/C=C/C(C)(C)CC2=C(C)[C@@H](OC(C)=O)[C@]3(C[C@@H](C)C=C3/C=C\1C)O2

Basic Information

ChEMBL ID CHEMBL2402300
Phase Preclinical
Structure Type MOL
InChI Key BMGXMFMQTBCDGL-ZBKWAGSWSA-N
5
Targets
6
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

400.5
MW (Da)
4.79
ALogP
5
HBA
0
HBD
61.8
PSA (Ų)
0.49
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H32O5
MW 400.52
Aromatic Rings 0
Heavy Atoms 29
NP-Likeness 2.01

Activity Summary

EC50 6 meas. best 5.25

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
EC50 5.25 5.035 5677.4 2
HepG2
CHEMBL395
EC50 4.58 4.58 26041.7 1
BJ
CHEMBL614358
EC50 4.58 4.58 26041.7 1
Raji
CHEMBL614628
EC50 4.58 4.58 26041.7 1
HEK293
CHEMBL614818
EC50 4.58 4.58 26041.7 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

Data from ChEMBL 36 via Core Engine