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Compound Detail

CHEMBL505378

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C[C@H]1[C@@H](CCCOP(=O)(OCCC[C@H]2O[C@@H]3O[C@@]4(C)CC[C@H]5[C@H](C)CC[C@@H]([C@H]2C)[C@@]35OO4)Oc2ccccc2)O[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3

Basic Information

ChEMBL ID CHEMBL505378
Phase Preclinical
Structure Type MOL
InChI Key SQOLELGMLMBYCG-VGPWWDKCSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

790.9
MW (Da)
9.27
ALogP
12
HBA
0
HBD
118.6
PSA (Ų)
0.11
QED
3
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H63O12P
MW 790.93
Aromatic Rings 1
Heavy Atoms 55
NP-Likeness 1.41

Activity Summary

IC50 2 meas. best 9.68

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 9.68 9.68 0.2 1
HL-60
CHEMBL383
IC50 6.6 6.6 250.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19136263 10.1016/j.bmc.2008.12.017 HL-60 1
19136263 10.1016/j.bmc.2008.12.017 Plasmodium falciparum 1

Data from ChEMBL 36 via Core Engine