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Compound Detail

CHEMBL260359

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CCCNCCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3[C@H](OC(C)=O)C[C@@H]4CC5(CC[C@]4(C)[C@H]3C[C@H](OC(C)=O)[C@]12C)OOC1(CCCCC1)OO5

Basic Information

ChEMBL ID CHEMBL260359
Phase Preclinical
Structure Type MOL
InChI Key GJJCSCGFBPISGV-BDXZXWPNSA-N
1
Targets
3
Activities
1
Assay Types
2
PK Parameters
3
Publications
0
Known Names

Molecular Properties

647.9
MW (Da)
7.41
ALogP
9
HBA
1
HBD
101.5
PSA (Ų)
0.16
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C37H61NO8
MW 647.89
Aromatic Rings 0
Heavy Atoms 46
NP-Likeness 1.83

Activity Summary

IC50 3 meas. best 7.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 7.96 7.7533 11.1 3

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.0 hr Homo sapiens
T1/2 1.0 hr Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18330976 10.1021/jm701417a Plasmodium falciparum 6
18330976 10.1021/jm701417a Liver microsomes 1
18330976 10.1021/jm701417a Liver 1

Data from ChEMBL 36 via Core Engine