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Compound Detail

CHEMBL4166340

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C/C1=C/C(=O)O[C@H](C(C)(C)C)CCC[C@H](O)CCC[C@H](O)CCC[C@H](O)CCC[C@@H]2C[C@H](C[C@H](O)CCC[C@@H](O)CCC[C@@H]3C[C@H](CCCCC1)OC(C)(C)O3)OC(C)(C)O2

Basic Information

ChEMBL ID CHEMBL4166340
Phase Preclinical
Structure Type MOL
InChI Key SHPUBKDPNPVFDX-IURFRBLBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

869.3
MW (Da)
9.89
ALogP
11
HBA
5
HBD
164.4
PSA (Ų)
0.15
QED
3
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C50H92O11
MW 869.27
Aromatic Rings 0
Heavy Atoms 61
NP-Likeness 0.84

Activity Summary

IC50 1 meas. best 5.01

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 5.01 5.01 9700.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Plasmodium falciparum IC50 = 9700.0 nM 5.01 Antimalarial activity against chloroquine-sensitive Plasmodium falciparum HB3 by... 29327931

Literature References

PubMed DOI Target Context # Activities
29327931 10.1021/acs.jnatprod.7b00917 Plasmodium falciparum 1

Data from ChEMBL 36 via Core Engine