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Compound Detail

CHEMBL3427537

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C[C@@]1(O)CC[C@H]2[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)[C@@H](C(=O)Cn4cc5c(n4)CCCC5)CC[C@@H]32)C1

Basic Information

ChEMBL ID CHEMBL3427537
Phase Preclinical
Structure Type MOL
InChI Key PDOZRVXKPBQAJH-MOYGJMECSA-N
3
Targets
4
Activities
2
Assay Types
3
PK Parameters
5
Publications
0
Known Names

Molecular Properties

438.7
MW (Da)
5.35
ALogP
4
HBA
1
HBD
55.1
PSA (Ų)
0.69
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H42N2O2
MW 438.66
Aromatic Rings 1
Heavy Atoms 32
NP-Likeness 0.92

Activity Summary

EC50 2 meas. best 6.75
IC50 2 meas. best 7.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
GABA-A receptor; anion channel
CHEMBL2093872
IC50 7.62 7.62 24.0 1
Unchecked
CHEMBL612545
IC50 7.52 7.52 30.0 1
GABA-A receptor; agonist GABA site
CHEMBL2109244
EC50 6.75 6.445 178.0 2

Pharmacokinetic Data

Parameter Value Units Species
CL 10.83 mL.min-1.kg-1 Homo sapiens
CL 55.67 mL.min-1.kg-1 Rattus norvegicus
CL 67.5 mL.min-1.kg-1 Mus musculus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
25799373 10.1021/acs.jmedchem.5b00032 No relevant target 3
25799373 10.1021/acs.jmedchem.5b00032 GABA-A receptor; agonist GABA site 2
25799373 10.1021/acs.jmedchem.5b00032 Liver microsome 2
25799373 10.1021/acs.jmedchem.5b00032 GABA-A receptor; anion channel 1
25799373 10.1021/acs.jmedchem.5b00032 Liver 1

Data from ChEMBL 36 via Core Engine