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Compound Detail

CHEMBL3264185

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CC(=O)N[C@@H]1CC[C@@]2(C)[C@@H](C1)C[C@@H](OC(C)=O)[C@@H]1[C@@H]2C[C@H](OC(C)=O)[C@]2(C)[C@@H]([C@H](C)CCCNCCCNc3ccnc4cc(Cl)ccc34)CC[C@@H]12

Basic Information

ChEMBL ID CHEMBL3264185
Phase Preclinical
Structure Type MOL
InChI Key UAGKUOLDGVTDRP-AFBSPGJWSA-N
3
Targets
5
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

737.4
MW (Da)
7.94
ALogP
8
HBA
3
HBD
118.7
PSA (Ų)
0.14
QED
2
Ro5 Violations
13
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C42H61ClN4O5
MW 737.43
Aromatic Rings 2
Heavy Atoms 52
NP-Likeness 1.08

Activity Summary

IC50 5 meas. best 7.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 7.89 7.6733 12.8 3
HepG2
CHEMBL395
IC50 5.84 5.84 1448.0 1
Botulinum neurotoxin type A
CHEMBL5192
IC50 5.31 5.31 4920.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
24742203 10.1021/jm500033r Plasmodium falciparum 8
24742203 10.1021/jm500033r Unchecked 3
24742203 10.1021/jm500033r Botulinum neurotoxin type A 2
24742203 10.1021/jm500033r HepG2 1

Data from ChEMBL 36 via Core Engine