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Compound Detail

CHEMBL3264507

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CC(=O)O[C@H]1C[C@H]2[C@@H]([C@H](OC(C)=O)C[C@@H]3C[C@H](N)CC[C@@]32C)[C@@H]2CC[C@H]([C@H](C)CCCN(CCCNc3ccnc4cc(Cl)ccc34)CCC[C@@H](C)[C@H]3CC[C@H]4[C@@H]5[C@H](OC(C)=O)C[C@@H]6C[C@H](N)CC[C@]6(C)[C@H]5C[C@H](OC(C)=O)[C@]34C)[C@@]12C

Basic Information

ChEMBL ID CHEMBL3264507
Phase Preclinical
Structure Type MOL
InChI Key LVJIFUYBDXSLLO-QXXFKIRTSA-N
3
Targets
5
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

1155.1
MW (Da)

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C68H104ClN5O8
MW 1155.06

Activity Summary

IC50 5 meas. best 6.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 6.66 6.6 217.8 3
Botulinum neurotoxin type A
CHEMBL5192
IC50 6.2 6.2 630.0 1
HepG2
CHEMBL395
IC50 5.67 5.67 2130.0 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