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Compound Detail

CHEMBL4646750

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CC1(C)[C@@H](O)CC[C@]2(C)[C@H]3CC=C4[C@@H]5C[C@](C)(CO)[C@@H](O)C[C@]5(C(=O)O)CC[C@@]4(C)[C@]3(C)[C@@H](O)C[C@@H]12

Basic Information

ChEMBL ID CHEMBL4646750
Phase Preclinical
Structure Type MOL
InChI Key PMQJDRVWSFKECR-BDXKCRPOSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

504.7
MW (Da)
4.15
ALogP
5
HBA
5
HBD
118.2
PSA (Ų)
0.36
QED
1
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H48O6
MW 504.71
Aromatic Rings 0
Heavy Atoms 36
NP-Likeness 3.08

Activity Summary

EC50 1 meas. best 5.11

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
PC-12
CHEMBL612556
EC50 5.11 5.11 7740.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
PC-12 EC50 = 7740.0 nM 5.11 Neuroprotective activity against CoCl2-induced neuronal injury in rat PC12 cells 31924497

Literature References

PubMed DOI Target Context # Activities
31924497 10.1016/j.bmcl.2019.126947 PC-12 1

Data from ChEMBL 36 via Core Engine