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Compound Detail

CHEMBL510825

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CC(=O)N[C@@H](CC(C)C)C(=O)N(C)[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@@H]5[C@H](C)N(C)C[C@@]54CC[C@@H]32)C1

Basic Information

ChEMBL ID CHEMBL510825
Phase Preclinical
Structure Type MOL
InChI Key YNZJHECUVVZSLB-JDEVNGBYSA-N
2
Targets
4
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

497.8
MW (Da)
5.26
ALogP
3
HBA
1
HBD
52.6
PSA (Ų)
0.53
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C31H51N3O2
MW 497.77
Aromatic Rings 0
Heavy Atoms 36
NP-Likeness 1.54

Activity Summary

Ki 4 meas. best 8.79

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H3 receptor
CHEMBL264
Ki 8.79 8.79 1.6 2
Histamine H3 receptor
CHEMBL4124
Ki 8.17 8.17 6.8 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18683917 10.1021/jm8003625 Histamine H3 receptor 4

Data from ChEMBL 36 via Core Engine