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Compound Detail

CHEMBL3084853

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CC(=O)O[C@H]1C[C@H]2[C@@H]([C@H](OC(C)=O)C[C@@H]3CC4(CC[C@@]32C)OOC2(CCC(C)CC2)OO4)[C@@H]2CCC(C(C)CCC(N)=O)[C@@]12C

Basic Information

ChEMBL ID CHEMBL3084853
Phase Preclinical
Structure Type MOL
InChI Key SFYMERLVGXDHSO-RAVTWPSQSA-N
2
Targets
5
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

633.8
MW (Da)
6.14
ALogP
9
HBA
1
HBD
132.6
PSA (Ų)
0.27
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H55NO9
MW 633.82
Aromatic Rings 0
Heavy Atoms 45
NP-Likeness 1.91

Activity Summary

IC50 5 meas. best 9.24

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 9.24 8.43 0.6 4
Vero
CHEMBL391
IC50 5.26 5.26 5510.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
12139444 10.1021/jm020891g Plasmodium falciparum 4
12139444 10.1021/jm020891g Mycobacterium tuberculosis 3
12139444 10.1021/jm020891g Vero 2

Data from ChEMBL 36 via Core Engine