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Compound Detail

CHEMBL218573

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CC(C)Cn1c(=O)n(C)c(=O)c2c(C(=O)N3C[C@H](O)CO3)c(Cc3ccccc3C(F)(F)F)sc21

Basic Information

ChEMBL ID CHEMBL218573
Phase Preclinical
Structure Type MOL
InChI Key GOSZMIDOMHVHDD-AWEZNQCLSA-N
3
Targets
3
Activities
2
Assay Types
2
PK Parameters
7
Publications
0
Known Names

Molecular Properties

511.5
MW (Da)
2.78
ALogP
8
HBA
1
HBD
93.8
PSA (Ų)
0.57
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H24F3N3O5S
MW 511.52
Aromatic Rings 3
Heavy Atoms 35
NP-Likeness -0.91

Activity Summary

IC50 2 meas. best 6.08
Ki 1 meas. best 10.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Monocarboxylate transporter 1
CHEMBL4360
Ki 10.05 10.05 0.1 1
Cytochrome P450 2C9
CHEMBL3397
IC50 6.08 6.08 830.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.08 5.08 8300.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 44.0 uL.min-1.(10^6cells)-1 Rattus norvegicus
CL - - Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Monocarboxylate transporter 1 Ki = 0.09 nM 10.05 Binding affinity to MCT1 17228867
Cytochrome P450 2C9 IC50 = 830.0 nM 6.08 Inhibition of CYP2C9 17228867
Cytochrome P450 3A4 IC50 = 8300.0 nM 5.08 Inhibition of CYP3A4 17228867

Literature References

PubMed DOI Target Context # Activities
17228867 10.1021/jm060995h ADMET 2
17228867 10.1021/jm060995h Monocarboxylate transporter 1 1
17228867 10.1021/jm060995h Cytochrome P450 2C9 1
17228867 10.1021/jm060995h Cytochrome P450 3A4 1
17228867 10.1021/jm060995h No relevant target 1
- 10.6019/CHEMBL3301361 No relevant target 1
- 10.6019/CHEMBL3301361 ADMET 1

Data from ChEMBL 36 via Core Engine