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Compound Detail

CHEMBL2057300

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C[C@]12CC[C@H](NS(N)(=O)=O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12

Basic Information

ChEMBL ID CHEMBL2057300
Phase Preclinical
Structure Type MOL
InChI Key QLIJDTTVUNSTPX-LUJOEAJASA-N
1
Targets
3
Activities
1
Assay Types
1
PK Parameters
5
Publications
0
Known Names

Molecular Properties

368.5
MW (Da)
2.76
ALogP
3
HBA
2
HBD
89.3
PSA (Ų)
0.79
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 C19H32N2O3S
MW 368.54
Aromatic Rings 0
Heavy Atoms 25
NP-Likeness 1.61

Activity Summary

IC50 3 meas. best 5.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Glucose-6-phosphate 1-dehydrogenase
CHEMBL5347
IC50 5.92 5.5333 1200.0 3

Pharmacokinetic Data

Parameter Value Units Species
t1/2 - - Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
22506561 10.1021/jm300317k Glucose-6-phosphate 1-dehydrogenase 3
22506561 10.1021/jm300317k Caco-2 2
22506561 10.1021/jm300317k Liver microsomes 2
22506561 10.1021/jm300317k No relevant target 1
35239352 10.1021/acs.jmedchem.1c01577 Glucose-6-phosphate 1-dehydrogenase 1

Data from ChEMBL 36 via Core Engine