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Compound Detail

CHEMBL5182318

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C=C(C)[C@@H]1CC[C@]2(NCC3CCCC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)Cc6c[nH]nc6C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12

Basic Information

ChEMBL ID CHEMBL5182318
Phase Preclinical
Structure Type MOL
InChI Key OIQHKTHIYPPKSK-LHEJOVJJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

531.9
MW (Da)
8.61
ALogP
2
HBA
2
HBD
40.7
PSA (Ų)
0.38
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H57N3
MW 531.87
Aromatic Rings 1
Heavy Atoms 39
NP-Likeness 1.71

Activity Summary

IC50 1 meas. best 4.83

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
RAW264.7
CHEMBL612557
IC50 4.83 4.83 14970.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
RAW264.7 IC50 = 14970.0 nM 4.83 Inhibition of RANKL/M-CSF-induced osteoclastogenesis in mouse RAW264.7 cells mea... 34491054

Literature References

PubMed DOI Target Context # Activities
34491054 10.1021/acs.jmedchem.1c01019 RAW264.7 1

Data from ChEMBL 36 via Core Engine