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Compound Detail

CHEMBL1559759

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O=C(Nc1cccc(Cl)c1)c1ccccc1

Basic Information

ChEMBL ID CHEMBL1559759
Phase Preclinical
Structure Type MOL
InChI Key HCMMPLSOWUBZAH-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
14
Publications
0
Known Names

Molecular Properties

231.7
MW (Da)
3.59
ALogP
1
HBA
1
HBD
29.1
PSA (Ų)
0.84
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C13H10ClNO
MW 231.68
Aromatic Rings 2
Heavy Atoms 16
NP-Likeness -1.78

Activity Summary

IC50 1 meas. best 5.06

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Plasmodium falciparum
CHEMBL364
IC50 5.06 5.06 8700.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Plasmodium falciparum IC50 = 8700.0 nM 5.06 Antiplasmodial activity against Plasmodium falciparum assessed as inhibition of ... -

Literature References

PubMed DOI Target Context # Activities
30392371 10.1021/acs.jmedchem.8b01293 GroEL/GroES 2
30392371 10.1021/acs.jmedchem.8b01293 Unchecked 2
30392371 10.1021/acs.jmedchem.8b01293 Staphylococcus aureus 2
38894921 10.1021/acsmedchemlett.3c00532 Amine oxidase [flavin-containing] B 2
- 10.1007/s00044-010-9323-4 Plasmodium falciparum 1
30392371 10.1021/acs.jmedchem.8b01293 Thiosulfate sulfurtransferase 1
30392371 10.1021/acs.jmedchem.8b01293 Enterococcus faecium 1
30392371 10.1021/acs.jmedchem.8b01293 Klebsiella pneumoniae 1
30392371 10.1021/acs.jmedchem.8b01293 Acinetobacter baumannii 1
30392371 10.1021/acs.jmedchem.8b01293 Pseudomonas aeruginosa 1
30392371 10.1021/acs.jmedchem.8b01293 Enterobacter cloacae 1
30392371 10.1021/acs.jmedchem.8b01293 HSP60/HSP10 1
30392371 10.1021/acs.jmedchem.8b01293 HEK293 1
38894921 10.1021/acsmedchemlett.3c00532 Amine oxidase [flavin-containing] A 1

Data from ChEMBL 36 via Core Engine