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Compound Detail

CHEMBL4063338

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C=C1CC[C@H]2[C@H](CC(C)C)C3=C(O[C@]2(C)CC[C@@H]2[C@@H]1CC2(C)C)C(C)(C)C(=O)C(C)(C)C3=O

Basic Information

ChEMBL ID CHEMBL4063338
Phase Preclinical
Structure Type MOL
InChI Key CUSDTBOAPLTSNT-LECQPLKFSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

454.7
MW (Da)
7.30
ALogP
3
HBA
0
HBD
43.4
PSA (Ų)
0.32
QED
1
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C30H46O3
MW 454.70
Aromatic Rings 0
Heavy Atoms 33
NP-Likeness 2.50

Activity Summary

IC50 1 meas. best 4.95

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 4.95 4.95 11300.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Plasmodium falciparum IC50 = 11300.0 nM 4.95 Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum 3D7 ... 28400231

Literature References

PubMed DOI Target Context # Activities
28400231 10.1016/j.bmcl.2017.03.065 Plasmodium falciparum 1

Data from ChEMBL 36 via Core Engine