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Compound Detail

CHEMBL1094991

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CC(C)(CN1C(=O)c2cccc3cc([N+](=O)[O-])cc(c23)C1=O)C[N+](C)(C)CCCCCC[N+](C)(C)CC(C)(C)CN1C(=O)c2cccc3cc([N+](=O)[O-])cc(c23)C1=O.[Br-].[Br-]

Basic Information

ChEMBL ID CHEMBL1094991
Phase Preclinical
Structure Type MOL
InChI Key UNUOYJOSFXYNPV-UHFFFAOYSA-L
Parent Compound CHEMBL1199149
Active Moiety CHEMBL1199149
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

795.0
MW (Da)
7.47
ALogP
8
HBA
0
HBD
161.0
PSA (Ų)
0.03
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H54Br2N6O8
MW 954.76
Aromatic Rings 4
Heavy Atoms 58
NP-Likeness -0.23

Activity Summary

IC50 1 meas. best 6.18

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 6.18 6.18 660.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Plasmodium falciparum IC50 = 660.0 nM 6.18 Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum 3D7 ... 20382538

Literature References

PubMed DOI Target Context # Activities
20382538 10.1016/j.bmc.2010.03.067 Plasmodium falciparum 2
20382538 10.1016/j.bmc.2010.03.067 ADMET 1

Data from ChEMBL 36 via Core Engine