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Compound Detail

CHEMBL3427540

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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)Cn4ncc5ccccc54)CC[C@@H]32)C1

Basic Information

ChEMBL ID CHEMBL3427540
Phase Preclinical
Structure Type MOL
InChI Key PNRLOCDAUHBIHX-MOYGJMECSA-N
4
Targets
5
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

434.6
MW (Da)
5.63
ALogP
4
HBA
1
HBD
55.1
PSA (Ų)
0.68
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 C28H38N2O2
MW 434.62
Aromatic Rings 2
Heavy Atoms 32
NP-Likeness 0.75

Activity Summary

EC50 3 meas. best 6.29
IC50 2 meas. best 7.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
GABA-A receptor; anion channel
CHEMBL2093872
IC50 7.82 7.82 15.0 1
Unchecked
CHEMBL612545
IC50 7.52 7.52 30.0 1
GABA-A receptor; agonist GABA site
CHEMBL2109244
EC50 6.29 6.05 508.0 2
GABA-A receptor; alpha-1/beta-2/gamma-2
CHEMBL2095172
EC50 5.82 5.82 1500.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

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

Data from ChEMBL 36 via Core Engine