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Compound Detail

CHEMBL392236

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CC(C)OC(=O)N1CCC(CN(C2Cc3cc(C#N)ccc3N(Cc3cncn3C)C2)S(=O)(=O)c2ccccn2)CC1

Basic Information

ChEMBL ID CHEMBL392236
Phase Preclinical
Structure Type MOL
InChI Key IUJQRRMVCBZZFE-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
7
Publications
0
Known Names

Molecular Properties

591.7
MW (Da)
3.57
ALogP
9
HBA
0
HBD
124.7
PSA (Ų)
0.39
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H37N7O4S
MW 591.74
Aromatic Rings 3
Heavy Atoms 42
NP-Likeness -1.38

Activity Summary

IC50 1 meas. best 9.3

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 9.3 9.3 0.5 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 6438.13 ng.hr.mL-1 Rattus norvegicus
Cmax 4500.0 nM Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 0.5 nM 9.3 Inhibition of Plasmodium falciparum protein farnesyltransferase by SPA method 17606674

Literature References

PubMed DOI Target Context # Activities
17722901 10.1021/jm0703340 Unchecked 3
17606674 10.1128/aac.00246-07 Rattus norvegicus 3
17722901 10.1021/jm0703340 Plasmodium falciparum 2
17606674 10.1128/aac.00246-07 Caco-2 1
17606674 10.1128/aac.00246-07 Unchecked 1
17606674 10.1128/aac.00246-07 Plasmodium falciparum 1
17606674 10.1128/aac.00246-07 Mus musculus 1

Data from ChEMBL 36 via Core Engine