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Compound Detail

CHEMBL384536

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CC(C)Cn1c(=O)n(C)c(=O)c2c(C(=O)N3C[C@H](O)CO3)c(Cc3c[nH]c4ncccc34)sc21

Basic Information

ChEMBL ID CHEMBL384536
Phase Preclinical
Structure Type MOL
InChI Key HMICMRQBKBXVSC-AWEZNQCLSA-N
3
Targets
3
Activities
2
Assay Types
2
PK Parameters
7
Publications
0
Known Names

Molecular Properties

483.6
MW (Da)
1.63
ALogP
9
HBA
2
HBD
122.5
PSA (Ų)
0.44
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H25N5O5S
MW 483.55
Aromatic Rings 4
Heavy Atoms 34
NP-Likeness -0.84

Activity Summary

IC50 2 meas. best 4.82
Ki 1 meas. best 9.37

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Monocarboxylate transporter 1
CHEMBL4360
Ki 9.37 9.37 0.4 1
Cytochrome P450 3A4
CHEMBL340
IC50 4.82 4.82 15000.0 1
Cytochrome P450 2C9
CHEMBL3397
IC50 4.77 4.77 17000.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 12.0 uL.min-1.(10^6cells)-1 Rattus norvegicus
CL 3.0 uL.min-1.(10^6cells)-1 Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Monocarboxylate transporter 1 Ki = 0.43 nM 9.37 Binding affinity to MCT1 17228867
Cytochrome P450 3A4 IC50 = 15000.0 nM 4.82 Inhibition of CYP3A4 17228867
Cytochrome P450 2C9 IC50 = 17000.0 nM 4.77 Inhibition of CYP2C9 17228867

Literature References

PubMed DOI Target Context # Activities
17228867 10.1021/jm060995h ADMET 2
- 10.6019/CHEMBL3301361 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

Data from ChEMBL 36 via Core Engine